Skip to main content

Natural products as potential drug treatments for acute promyelocytic leukemia

Abstract

Acute promyelocytic leukemia (APL), which was once considered one of the deadliest types of leukemia, has become a curable malignancy since the introduction of all-trans retinoic acid (ATRA) and arsenic trioxide (ATO) as clinical treatments. ATO, which has become the first-line therapeutic agent for APL, is derived from the natural mineral product arsenic, exemplifying an important role of natural products in the treatment of APL. Many other natural products, ranging from small-molecule compounds to herbal extracts, have also demonstrated great potential for the treatment and adjuvant therapy of APL. In this review, we summarize the natural products and representative components that have demonstrated biological activity for the treatment of APL. We also discuss future directions in better exploring their medicinal value, which may provide a reference for subsequent new drug development and combination therapy programs.

Introduction

The onset and treatment of acute promyelocytic leukemia

According to the latest World Cancer Report released by the International Agency for Research on Cancer of the World Health Organization (WHO), in 2020, there were 474,519 new cases of leukemia globally, accounting for 2.5% of all cancer cases, and 311,594 new leukemia deaths, accounting for 3.1% of all cancer deaths [1]. Acute promyelocytic leukemia (APL) is a subtype of leukemia that was first defined as a specific form of acute myeloid leukemia (AML) in 1957 [2]. APL accounts for 10–15% of AML cases [3]. APL is characterized by a severe tendency to hemorrhage in the early stage. The incidence of thrombosis in APL is higher than that of other types of leukemia, and the treatment process is susceptible to hemorrhage and hemothrombosis, which may lead to the death of patients [4, 5]. The bone marrow of patients with APL is dominated by abnormal granulocytic proliferation of promyelocytes, which accounts for more than 30% of non-erythroid nucleated cells. The pathogenesis of APL is related to chromosomal translocation. More than 98% of patients with APL have PML-RARα gene fusion, which is due to t (15;17) gene translocation, resulting in the fusion of promyelocytic leukemia (PML) on chromosome 15 with the gene encoding retinoic acid receptor-α (RARα) on chromosome 17, producing the fusion protein PML-RARα, which prevents cancer cell apoptosis [6, 7].

APL was once considered one of the deadliest types of leukemia due to its rapid disease progression and high early hemorrhagic mortality. Before the introduction of anthracyclines in the clinic, the survival of patients with APL was 3–16 weeks. The introduction of anthracyclines made the complete remission (CR) rate of APL comparable to that of other AML subtypes [8]. In the 1980s, both all-trans retinoic acid (ATRA) and arsenic trioxide (ATO) were first applied to the clinical treatment of APL by Chinese scholars, which led to epochal advances in the treatment and prognosis of this disease [9, 10], their mechanisms for treating APL is shown in Fig. 1. International authoritative guidelines, including the 2023 edition of the National Comprehensive Cancer Network Clinical Guidelines for Acute Myeloid Leukemia [11], the 2018 edition of the Chinese Guidelines for the Diagnosis and Treatment of Acute Promyelocytic Leukemia [3], and the Management of Acute Promyelocytic Leukemia by the Expert Panel of the European LeukemiaNet [12], recommend ATRA and ATO as first-line treatment options for APL. Due to the standardized clinical use of ATRA and arsenic agents, the treatment of APL does not rely on hematopoietic stem cell transplantation, and APL has become one of the most curable malignant diseases [13].

Fig. 1
figure 1

Mechanisms of ATRA and ATO in the treatment of APL. The PML-RARα fusion protein inhibits the differentiation and maturation of promyelocytes through dominant-negative inhibition. ATRA degrades PML-RARα, and ATO increases mitochondrial pore permeability, resulting in the release of apoptosis-inducing factor (AIF) and cytochrome C to the outside of the mitochondria, inducing apoptosis

APL treatment by traditional prescription

Before the introduction of standardized treatment, leukemia treatment in China often relied on the use of traditional Chinese medicine (TCM). Many early clinical observations have demonstrated that TCM has a beneficial impact on the treatment of leukemia. Ailing No.1 is an injection containing arsenolite and light powder. It is the predecessor of ATO injections, which are currently widely used as the first-line treatment of APL. Since the 1970s and 1980s, there have been clinical observations on the treatment of APL by the combination of Ailing No.1 and TCM dialectical treatment, achieving an overall effective rate of 78% and a CR rate of 59% [14]. Among the TCM prescriptions used were Lianhua Decoction, Xiangsha Six Gentlemen Decoction, Longdan Xiegan Decoction, Qinggu Powder, Angong Niuhuang Pill, Zixue Pill, etc., which can help regulate the immune system and prevent infections in clinical practice. Qinghuang powder, as a typical example, is a TCM prescription recorded in the Effective Formulae Handed Down for Generations (Yuan Dynasty) and Wonderful Well-Tried Recipes (Qing Dynasty), and its main ingredients are indigo naturalis and realgar. In the 1980s, Zhou et al. began using Qinghuang powder to treat acute non-lymphoblastic leukemia. They successfully cured two patients with M3, providing evidence of its beneficial impact on APL [15]. In the 1990s, clinical observations were conducted on the treatment of leukemia using a combination of Qinggu Powder and herbal medicines like Hedyotis diffusa, and the overall effective rate of this prescription in treating leukemia reached 84.6% [16]. Xiaochengqi Decoction from the Prescriptions for Universal Relief (Ming dynasty) plus Hedyotis diffusa and antibiotics can treat severe infections complicated by acute leukemia [17]. Since TCM prescriptions typically consist of natural medicines, the aforementioned clinical records demonstrate the positive impact of natural medicines in treating leukemia. With advancements in science and technology, numerous natural products found in traditional prescriptions have been proven to possess biological activity for APL treatment. Detailed discussions on some of the active ingredients are presented below. Table 1 displays several TCM prescriptions utilized for leukemia treatment.

Table 1 Traditional Chinese medicine prescriptions and their possible active ingredient in the treatment of leukemia

APL treatment by natural products

Natural medicines play an important role in the clinical treatment of APL in China. Arsenic and realgar, which are mineral medicines based on arsenic compounds, have been used as treatments for thousands of years. Nowadays, these two medicines are still utilized in the era of modern medicine. Arsenic acid, the aqueous solvent of the main ingredient of arsenic, is made into an injection and often combined with ATRA for the treatment of APL. There is no cross-resistance between ATRA and ATO, and patients with APL who are refractory to ATRA and conventional chemotherapeutic agents are still able to undergo treatment with ATO with good responses [18]. The oral arsenic, Realgar-Indigo Naturalis Formula (RIF), which is composed entirely of TCM with realgar as the main ingredient, is also widely used in clinical practice. In the Chinese Guideline for Diagnosis and Treatment of Childhood Acute Promyelocytic Leukemia published in the Chinese Journal of Applied Clinical Pediatrics in 2022, RIF is recommended as the first choice of arsenic agent [19].

Natural medicines play a unique role in the treatment of malignant tumors. In addition to RIF, which is compatible with wisdom, early clinical treatment of APL is often accompanied by TCM evidence-based treatment. This approach has achieved good therapeutic results, with few side effects and good therapeutic efficacy, supporting a great clinical application value [14]. The 2014 edition of the Chinese Guidelines for the Diagnosis and Treatment of Acute Promyelocytic Leukemia has also introduced homoharringtonine (HHT) [20]. HHT is an anti-leukemia drug for clinical application, which was first recommended in China. It is derived from Cephalotaxus and has anti-tumor activity [21]. In addition, as the therapeutic scope of ATO is often limited due to its cardiotoxicity and many natural medicines play a protective role in the treatment of ATO-induced cardiac side effects, natural medicines have broad prospects as cardioprotective agents against ATO-induced cardiac side effects [22].

Most natural products used in the treatment of cancer have multiple targets with multiple biological properties. Therefore, they can treat a wide range of diseases, making them preferable over single-target drugs [23]. Among the anti-tumor medicines used in clinical practice with high efficacy, 60% are obtained from natural products [24]. Identifying active ingredients from natural products and developing them into drugs for clinical use fully promotes the utilization of natural resources. In recent years, due to the continuous development of science and technology, the treatment of tumors has not been limited to traditional chemotherapy. Cell therapy, gene therapy, and other emerging treatment modalities have gradually increased the curative rate of malignant tumors, but the high cost of cell therapy has become a major concern. In light of this, the inexpensiveness, safety, and effectiveness of natural products make them a viable option for the treatment of malignant tumors, such as leukemia. Focusing on APL, this review attempts to summarize the natural medicines with therapeutic potential for APL, which is expected to serve as an updated reference for future drug development.

Natural medicines currently used for APL treatment

Arsenic and realgar derived from minerals

Mineral medicines are non-renewable resources that encompass natural minerals, processed minerals, and fossilized animal bones. China has a long history of using mineral medicines, and the Soil Department and the Gold and Stone Department in the Compendium of Materia Medica have recorded the use of various types of mineral medicine, including realgar, orpiment, and arsenic, which contain arsenic as their main active ingredient. In the periodic table, the element As (arsenic) is located below P (phosphorous), belonging to the VA group. As such, arsenic compounds are similar to phosphorus in many ways. For example, the common oxidation state is As (III) and As (V), the state in nature is generally As2O3, and it can form As (OH)3 or its corresponding arsenite (AsO2-) in water. Of these, As (V) is less toxic, and its biological activity is based primarily on phosphate substitution [25]. At present, both arsenic and realgar are used as first-line treatments for APL, especially ATO injection, the efficacy of which is widely recognized worldwide.

The “poison”—ATO

In China, the use of arsenic as a treatment for leukemia dates back to the 1970s [26]. Dr. Tingdong Zhang of the First Affiliated Hospital of Harbin Medical University was inspired by a rural doctor’s prescription for treating skin cancer and used arsenic, light powder, and bufalin to configure a prescription for the small-range treatment of cancer. The patients achieved different degrees of improvement, and it was later confirmed that the active ingredient in the prescription was arsenic. Later, it was found that the efficacy of arsenic alone was comparable to the original formula, and, ATO, the main component of arsenic, was therefore directly used to design ATO injections [27]. Arsenic was previously considered as a highly toxic drug, and its use in clinical practice was limited to oral or topical application. China was the first country to develop it into an intravenous solution for the treatment of leukemia [6]. Nowadays, the treatment of APL is standardized, and ATRA combined with ATO could achieve an APL cure rate of more than 90% [28]. A prospective randomized clinical trial of ATRA-ATO/ATRA-chemotherapeutic agents (NCT01987297) showed that disease-free survival (DFS) was achieved in 96.1% of patients in the ATO group compared with 92.6% in the non-ATO group, and the 7-year relapse rate was significantly lower in the ATO group. During consolidation follow-up, grade 3–4 hematologic toxicity was significantly reduced in the ATO group. This shows that ATRA-ATO is not inferior to ATRA-chemotherapy in consolidating replacement chemotherapy and chemotherapy reduction [29]. According to the latest recommendations of the Expert Panel of European LeukemiaNet, the use of ATO in children with APL not only reduces exposure to high cumulative doses of anthracyclines, thereby reducing some long-term side effects, but it also improves outcomes in populations with a higher prevalence of high-risk disease [12]. Additional clinical trials have shown that ATRA-ATO has significantly greater and durable anti-leukemic efficacy than ATRA-chemotherapeutic agents in low-/intermediate-risk APL, and the advantages of ATRA-ATO will likely be demonstrated over time [30].

Arsenic, as a traditional medicine, is known for its toxicity. Arsenic is one of the 10 chemicals listed by the WHO as being a major public health concern. Inorganic arsenic has been recognized as a carcinogen and is the most significant chemical contaminant in drinking water worldwide [31]. In terms of whether the use of ATO will aggravate the burden in patients with APL, pharmacokinetic studies in Japan have demonstrated that ATO is metabolized when administered intravenously to patients with APL and that its methylated metabolites are rapidly eliminated from the bloodstream and excreted into the urine upon dosing completion, indicating no measurable accumulation of ATO in the bloodstream [32]. Hepatotoxicity, particularly in terms of increased liver enzymes, is often reported with the use of ATO. However, this type of hepatotoxicity is largely reversible and can be successfully managed by reducing or temporarily discontinuing ATO, and fatal liver failure has rarely been reported [33].

Although intravenous administration has become an effective treatment route for ATO, there is an emerging trend toward the use of oral ATO. Oral ATO does not put patients at risk of developing venous thrombosis, which can lead to a much better quality of life and convenience for patients, as well as reducing the burden on healthcare facilities compared with intravenous administration [34]. Ventricular arrhythmias occur in approximately 30% of patients during intravenous administration of ATO. When arsenic is administered orally, peak plasma arsenic is decreased and cardiotoxicity is relatively low [35]. Oral arsenic has obvious safety advantages, and if reliable clinical trials prove that it is not less effective than intravenous ATO, oral arsenic will be a great advancement in the treatment of APL.

Realgar as another arsenic compound

Realgar is a mineral medicine that is commonly used in TCM, and its main component is As2S2 with a small amount of As2O3 and other metal salts. In 1980, Shilin Huang, a professor at the 210th Hospital of the People’s Liberation Army, formulated a pure TCM complex formula, namely Fufang Huangdai Tablet (RIF). RIF follows the important formula of “Monarch, Minister, Assistant and Envoy,” as shown in Fig. 2, with realgar as the “Monarch,” indigo naturalis as the “Minister,” and Salvia miltiorrhiza and radix Pseudostellariae as the “Assistant and Envoy” [36]. Realgar is the main component in the formula, and its main active ingredient is As2S2, which induces apoptosis in NB4 cells and HL-60 cells, and its effect is enhanced with time and concentration within certain ranges [37, 38]. Indigo naturalis increases the efficacy of realgar, and the combination of Salvia miltiorrhiza and Radix Pseudostellariae can reduce arsenic toxicity [39]. There is also clinical evidence showing that RIF used in combination with ATO is less cardiotoxic than intravenous ATO alone, and oral RIF also reduces the incidence of infection compared with ATO [40]. A clinical trial examining the efficacy of intravenous ATO versus oral RIF demonstrated that RIF-ATRA was not inferior to ATO-ATRA for the treatment of patients with non-high-risk APL. This study suggests that a completely oral, chemotherapy-free model may be an alternative to standard intravenous therapy for patients with non-high-risk APL [41].

Fig. 2
figure 2

RIF follows the important formula of “Monarch, Minister, Assistant, and Envoy”. Realgar induces apoptosis in NB4 cells and HL-60 cells, indigo naturalis increases the efficacy of realgar, and the combination of Salvia miltiorrhiza and radix Pseudostellariae reduces arsenic toxicity

RIF was the first commercially available oral arsenic agent approved in China, and it is commercially available in mainland China, with no license for use in other regions. The treatment of APL in the majority of patients is moving toward being completely oral without the use of chemotherapy. Oral RIF with ATRA will ultimately make treatment safer, reduce the economic burden, and increase the accessibility to more patients [33, 42].

HHT derived from Cephalotaxus

HHT is a new anti-leukemia drug that is recommended for clinical application and was first recommended in China [43]. Chinese people have used Cephalotaxus to treat tumors for a long time. HHT is derived from Cephalotaxus, and it is a natural plant alkaloid with anti-tumor activity [44]. HHT inhibits protein synthesis in eukaryotic cells. In addition to its anti-tumor activity, HHT induces leukemia differentiation and maturation and promotes leukemia cell apoptosis. After intravenous injection, the highest concentration of HHT was found in the bone marrow, followed by the kidneys, liver, spleen, heart, and gastrointestinal tract, while the lowest concentration was found in muscle and brain tissue. After 2 h of intravenous administration, the drug concentration in all tissues decreased rapidly, while the concentration in the bone marrow decreased more slowly [45].

The clinical application of HHT has proven efficacious. In the early years, the use of the HA regimen (HHT combined with cytosine arabinoside, Ara-C) for the treatment of AML achieved significant efficacy, and HHT has demonstrated no cross-resistance with Daunorubicin (DNR), Ara-C, and mercaptopurine [46, 47]. HHT is recommended in the consolidation phase in the current APL diagnosis and treatment guidelines in China [3, 20]. A clinical study showed no significant difference in the treatment efficacy of HHT and DNR in patients with APL, but HHT-treated patients had a better quality of life [48]. Another retrospective study showed that induction therapy with ATRA-HHT for APL resulted in a CR rate of up to 100%, with no deaths during induction therapy, and 9-year DFS and overall survival rates of 79.0% and 83.0%, respectively. Moreover, this regimen was well tolerated and hepatotoxicity could be recovered therapeutically. No serious cardiac or renal toxicity was observed, and no secondary tumors occurred during the follow-up period. Therefore, this regimen may be a highly effective therapeutic option for patients with newly diagnosed APL [49]. The reasons for choosing HHT go beyond its efficacy. A clinical trial of HHT in combination with ATRA and ATO for the treatment of economically disadvantaged patients with initial APL demonstrated lower healthcare costs in the HHT group due to fewer blood transfusions and a lower incidence of infections compared with the commonly used Idarubicin (IDA). HHT also has fewer cardiotoxic side effects in pediatric patients, elderly patients, and patients with a history of cardiac disease [50]. HHT in combination with other medications for the treatment of APL is effective and safe, and it is therefore one of the choices in the clinic.

Natural medicines with therapeutic potential for APL

Although ATRA and ATO are well-established treatment options for APL, the occurrence of various adverse effects still seriously affects the quality of life of patients. ATRA induces terminal differentiation of leukemia cells and significantly improves the prognosis of patients with APL. However, the continued use of drugs, such as ATRA, usually causes significant treatment-related toxicity, resulting in ATRA resistance, retinoic acid syndrome (RAS), hypercalcemia, and decreased plasma drug concentrations [51]. Natural drugs are usually characterized by low toxicity and multi-pathway action, and they are more biocompatible than chemical drugs. Therefore, natural products can be used as a potential complementary resource to chemotherapeutic drugs.

Small-molecule compounds with therapeutic potential for APL

Honokiol

Magnolia officinalis and Magnolia obovata bark extracts have been utilized as traditional medicines in China and Japan for centuries. These extracts are commonly employed in traditional medicine to address various health conditions, offering sedative, antioxidant, anti-inflammatory, antibiotic, and spasmodic effects. Additionally, they exhibit significant anticancer potential while maintaining low toxicity towards healthy cells. Honokiol (HKL) and magnolol (MAG), as shown in Fig. 3, are natural lignans with multiple effects that can be extracted from Magnolia grandiflora. Their safety and efficacy have gained widespread recognition [52, 53].

Fig. 3
figure 3

Structure of HKL and its analogue MAG

Although both HKL and MAG are active ingredients extracted from Magnoliaceae, NB4 cells are more sensitive to HKL than MAG, which significantly reduces the activity of NB4 cells. Interestingly, the pathway of HKL-induced NB4 cell death does not involve apoptotic features, such as caspase activation and nucleus fragmentation, and its apoptosis-inducing process is accompanied by increased reactive oxygen species (ROS), mitochondrial damage, and expansion of the endoplasmic reticulum by triggering the accumulation of misfolded and unfolded proteins. This induces extensive cytoplasmic vacuolization and NB4 cell apoptosis. As cancer cells can evade apoptotic cell death through a variety of adaptive mechanisms, HKL, which induces cancer cell death in a non-apoptotic manner, could be an important drug for the treatment of APL [54].

In addition to inducing apoptosis, HKL is effective when used in combination with other therapies. In the treatment of myeloid leukemia, the combination of HKL with low-concentration chemotherapeutic agents has significant synergistic cytotoxic effects, which can effectively reverse drug resistance and reduce drug toxicity [55]. Moreover, HKL has a significant synergistic effect with cytarabine for the treatment of AML, where it inhibits cell proliferation and induces apoptosis [56]. However, the effect of this regimen on APL has not been confirmed. In the treatment of APL, HKL counteracts the toxic effects of ATO on the cardiac mitochondria and exerts cardioprotective effects against ischemia/reperfusion chemistry-induced cardiotoxicity. This result was confirmed in a mouse model, in which mice pretreated with HKL demonstrated significant amelioration of ATO-induced myocardial apoptosis, cardiac dysfunction, and cardiac remodeling [57]. Therefore, the combination of ATO and HKL for the treatment of APL may achieve good safety.

Sesquiterpene lactones

Sesquiterpene lactones are a class of secondary metabolites. They are a large group of naturally occurring compounds with a wide range of notable biological properties, such as anti-inflammatory, anti-bacterial, and anti-tumor properties. Sesquiterpene lactones are mostly derived from the Compositae family, and families such as Cactaceae, Solanaceae, and Euphorbiaceae may also contain sesquiterpene lactones. Many of the active constituents of traditional medicinal plants used for various ailments, such as infections, inflammation, and headaches, contain sesquiterpene lactones [58]. Their main anti-tumor mechanisms include oxidative stress, iron death, induction of apoptosis, and cellular autophagy. Aucklandia lappa Decne. from the Asteraceae family, which has been used in the combinatorial treatment of leukemia in Xiangsha Six Gentlemen Decoction, contains the sesquiterpene lactone compound dehydrocostus lactone (DL). DL can enhance TNF-α-induced apoptosis and has anti-leukemia activity in vitro [59]. The natural products of sesquiterpene lactones not only inhibit drug-resistant tumor cells, but also present sensitizing and potentiating effects when used in combination with other drugs. However, current research on drug-resistant cells and drug combinations is still limited [58]. Sesquiterpene lactones, such as gaillardin and artesunate, also show therapeutic potential for APL. Chemical structures of the sesquiterpene lactone compounds DL, gaillardin, and artesunate are shown in Fig. 4.

Fig. 4
figure 4

Chemical structures of the sesquiterpene lactone compounds gaillardin and artesunate (ART), which consist of three isoprenoid units and usually have multiple biological properties

Gaillardin

Inula sesquiterpene lactones are a kind of sesquiterpene lactones extracted from Inula species. They have many pharmacological activities such as anti-inflammation, anti-asthma, anti-tumor, neuroprotection, and anti-allergy. The Inula genus has long been used in folk medicine to treat various ailments including kidney stones, urethral infections, jaundice, bronchitis, respiratory diseases, and cancer. It is widely utilized as a traditional medicine across Asia, the Middle East, Europe, and North America. In recent years, numerous studies have increasingly demonstrated the significance of these drugs as potential candidates for treating various types of cancers due to their strong anti-tumor activity [60,61,62]. Gaillardin, a sesquiterpene lactone isolated from the chloroform extract of Inula oculus-christi L., is toxic to a variety of cancer cells. It has been demonstrated that gaillardin induces cytotoxicity through the G0/G1 phase blockade and then apoptosis in a dose-dependent manner and that it has no significant cytotoxic effect on healthy cells, making it a promising anti-hematological malignancy medicine that could open new avenues for the treatment of APL [63].

In vitro experiments further support this idea. In a previous study, gaillardin dose-dependently induced apoptosis in APL cells. Gaillardin extracts at concentrations of 1, 4, and 5 μM induced early apoptosis in 10.5%, 19%, and 32% of NB4 cells, respectively, with an IC50 of approximately 7 μM after 48 h. Treatment of NB4 cells with gaillardin resulted in the upregulation of Bax transcripts and a decrease in Bcl-2 mRNA, in turn increasing the Bax/Bcl-2 transcription ratio. At the tissue level, Bcl-2 and Bax dimers formed, which initiated the release of cytochrome C from the mitochondria and activated caspase-3, ultimately leading to cell death [64]. In vivo experiments evaluating the treatment of APL with gaillardin are expected.

Artesunate

Artemisinin analogs, with their unique peroxy-bridge structure, have been shown to have significant therapeutic effects against Plasmodium falciparum, which causes malaria, and are not susceptible to drug resistance [65]. One of the herbs in the Chinese prescription Qinggu Powder is Artemisia annua L. In leukemia, artemisinin has been shown to induce cell cycle arrest [66]. Artesunate (ART) is a semi-synthetic derivative of artemisinin, which has the advantages of oral administration and good water solubility. It is widely used clinically for the treatment of malaria and has shown anti-tumor effects against a variety of hematologic tumors. Studies have shown that, after the treatment of NB4, HL-60, and NB4-R1 (retinoic acid-resistant strains) with 2, 10, or 20 μg/mL ART for 12, 24, or 48 h, cell proliferation was significantly inhibited in an obvious time- and concentration-dependent manner and the cells showed typical apoptotic morphology changes after 24 h. The mechanism of action of ART may be phosphorylation of the JNK pathway in the form of p-JNK, p-MKK4, and p-ATE-2, as well as inhibition of PI3K/AKT/mTOR pathway phosphorylation [67]. ART shows potential for the treatment of APL and retinoic acid-resistant APL, but its therapeutic efficacy needs to be further demonstrated.

Celastrol

Celastrol is a natural pentacyclic triterpenoid purified from the Celastraceae family. Celastrol possesses a variety of properties as a TCM, including anti-inflammatory and broad-spectrum anti-cancer properties [68]. Celastrol achieves its anti-malignant properties against hematological neoplasm through several pathways. First, celastrol is a potent low-molecular-weight inhibitor that induces myeloid differentiation and cancer cell apoptosis by inhibiting Myb activity. In combination with other compounds, the inhibitory effect of celastrol on cell proliferation can be enhanced [69]. Second, several studies have proven that celastrol can induce apoptosis in APL cells through the p53-activated mitochondrial pathway [70]. As shown in Fig. 5, the mRNA expression of caspase-9, caspase-3, and Bax was elevated after celastrol treatment, while the mRNA expression of p53 was not. The protein expression of cleaved caspase-9, cleaved caspase-3, Bax, and p53 was significantly elevated. After 24 and 48 h, inhibition of HL-60 cell proliferation occurred in a dose-dependent manner, with IC50 values of 0.48 and 0.55 μM at 24 and 48 h.

Fig. 5
figure 5

Celastrol induces apoptosis in APL cells through the mitochondrial pathway, causing changes in cytokines

Celastrol has a satisfactory safety profile in the treatment of APL. In the nude mouse model of APL with tumor xenografts, there was no significant difference in the coefficients of the heart, liver, spleen, lungs, kidneys, brain, testes, and epididymides between the control and celastrol-treated groups of mice. There were no statistically significant differences between the alanine transaminase (ALT), aspartate transaminase (AST), blood urea nitrogen (BUN), and creatinine concentrations (CREA) of control mice and celastrol-treated mice, which were all within normal ranges, and no obvious histopathology was seen in the testes of mice, suggesting that celastrol has no toxic effects on the liver, kidneys, or reproductive system at a dose of 2 mg/kg [70]. Additional in vitro results showed that the ability of leukemia cells from two different AML mouse models to form colonies in the semisolid medium was inhibited by sub-micromolar concentrations of celastrol, but the proliferative capacity of normal hematopoietic progenitor cells from healthy mice was not inhibited under the same conditions. Similarly, colony formation assays performed on leukemic cells from patients with AML and cells from healthy donors confirmed that leukemic cell proliferation was significantly inhibited by celastrol, whereas healthy progenitor cells were unaffected [69]. These results suggest that celastrol has a good safety profile in the treatment of leukemia and is a useful alternative combination therapy.

Tanshinone IIA

Salvia miltiorrhiza Bunge is an important component of oral arsenic agent RIF. Tanshinone IIA (Tan IIA) is a diterpene quinone isolated from Salvia miltiorrhiza Bunge, which is the most abundant and structurally representative fat-soluble constituent of Salvia miltiorrhiza, and has been found to possess anti-tumor properties, such as inducing cell autophagy and apoptosis, and inhibiting tumor invasion and metastasis [71]. Many studies have proven that Tan IIA has the biological activity to treat APL by inducing apoptosis in the APL cell line NB4 [72]. It has also shown excellent therapeutic effects when combined with ATRA and ATO.

In a previous study, Tan IIA inhibited the growth of NB4 cells and induced the differentiation of NB4 cells, and these effects were gradually enhanced with an increase in drug concentration and a prolonged duration of action. Similar to As2O3 and ATRA, Tan IIA did not change the expression of PML-RARα mRNA, but it degraded the PML-RARα fusion protein and restored the expression of the PML protein. The optimal concentration to achieve this effect was 2.55 μmol/L [73]. In addition, Tan IIA induced NB4 cell autophagy to form the autophagic stream in a concentration- and time-dependent manner. The effects of Tan IIA on NB4 cells, evaluated after 48 h., included significantly reduced expression of the autophagy-related protein p62, and increased autophagy rate of NB4 cells. PI3K-Akt, and mTOR protein bands in NB4 cells were less pronounced than those in the control group after treatment with Tan IIA, which indicated that Tan IIA reduced the expression of the PI3K-I, Akt, and mTOR proteins in NB4 cells. In short, Tan IIA reduced the Akt and mTOR phosphorylation levels, and inhibited PI3K/Akt/mTOR signaling [74]. Thirdly, when Tan IIA was combined with ATO, the apoptosis and autophagy rates of NB4 cells were higher than those of the single-drug group. This may be due to the fact that Tan IIA-ATO can upregulate the expression of the apoptosis-specific protein caspase-3 and the autophagy-specific protein LC3-II in transplanted tumor tissues, as well as enhancing tumor cell apoptosis and autophagy. Therefore, the Tan IIA-ATO combination has a chemo-sensitizing effect on NB4 transplanted tumors. In addition, experiments have shown that the Tan IIA-ATO regimen causes no obvious pathological damage to the bone marrow, heart, liver, lungs, kidneys, lymph nodes, and other important tissues and organs in nude mice, demonstrating its safety [75]. Fourth, as shown in Fig. 6, Tan IIA still has a therapeutic effect in ATRA-resistant strains. MR-2 is an ATRA-resistant APL cell type. When Tan IIA was co-cultured with NB4 and MR-2 cells, Tan IIA caused differentiation and apoptosis of both cell types, which indicated that there was no cross-resistance between ATRA and Tan IIA. Tan IIA at 1.0 mg/L inhibited the proliferation of MR-2 cells and induced their transformation into granulocytes, which is the most effective way to prevent the proliferation of ATRA [76]. Tan IIA at 1.0 mg/L inhibited the proliferation of MR-2 cells and induced their differentiation to the mature stage of the granulosa lineage, and the effect was comparable to that of 0.5 mg/L Tan IIA, which induced the differentiation of NB4 cells [77]. From the above studies, it is clear that Tan IIA may be a promising clinical treatment for APL, especially for recurrent and drug-resistant patients.

Fig. 6
figure 6

Tan IIA is therapeutically effective against both NB4 and MR-2, without cross-resistance

Oleanolic acid and its derivatives

Oleanolic acid (OA), a pentacyclic triterpenoid that is ubiquitous in the plant kingdom, is the main active ingredient of Akebia quinate (Thunb.) Decne. in Longdan Xiegan Decoction, Forsythia suspensa (Thunb.) Vahl in Lianhua Decoctio and Hedyotis diffusa. OA has been endowed with an extensive variety of biological properties and therapeutic potential through its complex and multi-factorial mechanisms, and it has received much attention from the scientific community because of its biological activity in a wide range of diseases. OA and related triterpenes have a wide range of pharmacological properties, but their therapeutic potential has only been partially exploited to date [78]. The anti-cancer potential of bioactive triterpenes in vitro and in vivo models, including in the treatment of APL, has been widely discussed [79].

OA enhances the differentiation of APL cells and prevents the development of leukemia in mice [80]. Firstly, OA and its analog ursolic acid (UA) significantly inhibited the proliferation of HL-60 cells in a concentration- and time-dependent manner from 0 to 72 h after treatment. The number of non-living cells was higher for cells cultured at high OA and UA concentrations of 80–100 μM. At non-cytotoxic concentrations, OA had a more significant differentiation-inducing effect on HL-60 cells, and when combined with low-dose ATRA, OA increased the differentiation rate of HL-60 cells, whereas UA had no significant effect on the differentiation of ATRA. In a mouse model of leukemia, OA increased the survival time and decreased the infiltration of leukemia cells into the liver and kidneys.

The structures of OA and its derivatives are shown in Fig. 7. The OA derivatives DIOXOL and HIMOXOL may also be therapeutically effective against HL-60 cells, its overexpressing subline HL-60/AR, and its multidrug-resistant subline ABCC1. DIOXOL and HIMOXOL are the most potent semi-synthetic OA derivatives against human APL cells [81]. Cell cycle analyses of 5–20 μM DIOXOL and HIMOXOL treatment for 24 h showed the presence of sub-G1 cell populations, indicating DNA fragmentation of dead cells. Among them, DIOXOL was the most effective at inducing apoptosis in HL-60 cells, and higher concentrations of DIOXOL (10 μM and 20 μM) activated apoptosis to a greater degree than HIMOXOL. DIOXOL significantly reduced p65 nuclear factor kappa-B (NF-κB) and inhibited its translocation to the nucleus to activate the apoptotic program. A 70% reduction in intracellular NF-κB subunit content was observed in samples treated with 20 μM DIOXOL. HIMOXOL is the most effective compound against drug-resistant HL-60/AR cells. It can inhibit ABCC1 transporter function in a short period and reduce ABCC1 protein expression over a longer period. HIMOXOL at concentrations of 5 and 10 μM were able to act at the transcriptional level, leading to significant reductions in ABCC1 transcripts of approximately 30% and 50%. HIMOXOL was also more effective at reducing the amount of Bcl-2. Bcl-2 was reduced by 15% when HIMOXOL was used at a concentration of 10 μM, which was increased to 70% when HIMOXOL was used at a concentration of 20 μM. OA and its derivatives could be used as part of an initial screen of potential synergistic anti-leukemic agents for ATRA, providing a direction for new APL drug development.

Fig. 7
figure 7

Structure of OA and its derivatives, which all have therapeutic potential for APL

Active extracts from plants

Natural seaweed extracts—fucoidan

Fucoidan is a high molecular-weight, fucose-based, sulfated polysaccharide extracted from the brown macroalgae. It is a natural component of seaweed and is found in the cell walls of a range of brown seaweeds. Fucoidan is a heterogeneous sulfated polysaccharide containing sulfated L-fucose with 34–44% fucose content, which has immunomodulatory and anti-tumor effects [82, 83].

In a previous study, fucoidan inhibited the proliferation and induced the apoptosis of the APL cell lines NB4 and HL-60 via both endogenous and exogenous pathways. The proliferation of NB4 and HL-60 cells was inhibited in a dose-dependent manner, and the cell proliferation of HL-60 and NB4 cells decreased to less than 10% at fucoidan concentrations of 50 and 25 μg/mL, respectively. After treatment of NB4 and HL-60 cells with 100 μg/mL fucoidan for 48 h, the percentage of sub-G0/G1 cells in the dead cell population increased significantly in a time-dependent manner, and fucoidan significantly increased apoptosis in both cell lines. After 10 days of inoculation of NB4 cells into seven nude mice in each of the two groups, five in the control group developed subcutaneous tumors, whereas only two in the fucoidan group developed subcutaneous tumor masses, and no other toxicity was observed in either group [84]. These findings collectively suggest that fucoidan significantly delays tumor growth.

The conventional therapy for APL is ATRA-ATO, but drug resistance or RAS may occur with long-term use of this regimen. Some findings suggest that, by adding fucoidan to the standard APL regimen, the number of resistant cells in patients who respond to ATRA can be limited [85]. Fucoidan combined with the ATRA-ATO regimen synergistically induced NB4 cell differentiation, as evidenced by increased CD11b expression and G0/G1 blockade. In vitro findings showed that a portion of cells remained undifferentiated when cells were treated with ATRA alone or ATRA-ATO, whereas almost all cells underwent differentiation when fucoidan was combined with ATRA-ATO. CD44 expression in APL cells was reduced when mouse tumor cuts were treated with fucoidan combined with ATRA, implying that the use of this regimen may decelerate the spread of cancer cells in patients with APL. The use of fucoidan as a supplement to standard APL therapy may represent a promising new strategy for APL management.

Crocin and crocetin from saffron

Saffron is derived from Crocus sativus L., which is a valuable medicinal plant in many traditional medicinal cultures. There are around 75 species of crocus in the world, and saffron is the only species available for medicinal use. It is mainly distributed in Southern Europe and Iran, and also planted in China [86]. Saffron has more than 200 active ingredients, including pigments, flavonoids, phenolic acids, and fatty acids, amongst others [87]. Gardenia jasminoides Ellis, commonly used in TCM, is one of the components of Longdan Xiegan Decoction, and also contains similar components. The Compendium of Materia Medica describes saffron as “The smell is sweet, flat, and non-toxic. Indications: Heart worries and stagnation, persistent Qi stagnation, and promoting blood circulation. Long-serving brings joy and treats palpitations.” Among the active ingredients, crocin (CRO) and crocetin (CRT) have great potential for the treatment of APL. The activity mechanism of CRO and CRT is shown in Fig. 8.

Fig. 8
figure 8

The bioactive substances CRO and CRT in saffron. CRO inhibits the proliferation and tumorigenicity of HL-60 cells. CRT has anti-oxidant and anti-apoptotic properties and can significantly reduce oxidative stress in ATO-induced nephrotoxicity

CRO is the main water-soluble carotenoid in saffron extract. It has anti-tumor activity against many human tumors [88]. Studies have shown [89] that CRO at a certain concentration range (0.625–10 mg/mL) significantly inhibits the proliferation of HL-60 cells, and with an increase in the CRO concentration from 0.625 to 5 mg/mL, the percentage of apoptotic cells increases significantly, and this effect is time-dependent. In the nude mouse HL-60 cell model, the tumor formation time in the experimental group (6.25 mg/kg CRO) was significantly longer than in the other groups, and the tumor formation time in the experimental group (25 mg/kg CRO) was longer than in the control group and the experimental group (100 mg/kg CRO). Compared with the control group, the rate of change in tumor weight and tumor size was significantly suppressed in mice treated with 6.25 and 25 mg/kg CRO. Moreover, Bcl-2 protein expression was reduced and Bax protein expression was elevated in the tumor. The above findings prove that CRO inhibits the proliferation and tumorigenicity of HL-60 cells.

In addition to its therapeutic potential, CRO in combination with ATO reduces ATO-induced cardiotoxicity [90]. CRO administration not only reduces QTc interval prolongation, cardiac enzymes, and troponin T, but it also improves histopathological results. The expression of Bax and caspase-3 in the myocardium of rats treated with CRO was significantly decreased compared to when rats without CRO. CRO appears to reduce ATO-induced myocardial pathological changes, and the therapeutic effect of CRO appears to be dose-dependent. Similarly, CRT may be protective against ATO-induced renal injury [91]. CRT has anti-oxidant and anti-apoptotic properties, and therefore it can significantly reduce oxidative stress in ATO-induced nephrotoxicity. In one study, ATO-induced histopathological changes in the kidneys of rats showed glomerular destruction, tubular cell swelling, interstitial fibrosis with inflammatory cell infiltration, and nephrocyte atrophy and necrosis. Treatment with 25 or 50 mg/kg CRT significantly reduced the morphological changes in the kidney induced by ATO. From the above, it is reasonable to propose that CRO and CRT are ideal choices as combined treatments with ATO, and the usefulness of these combinations should be further investigated for clinical application.

Green tea extract

Tea is one of the most popular drinks in the world. Originating from China, tea was introduced to the world thousands of years ago via the Silk Road. The production of green tea involves decoction or steaming of freshly harvested leaves to inactivate polyphenol oxidase and other enzymes that prevent fermentation/oxidation, preserving the active chemical properties [92]. As one of the most consumed beverages worldwide, green tea has been the focus of much research, and its polyphenolic compounds have been shown to have many benefits for human health. Catechins are the main components extracted from green tea leaves and are present in about 30% of dried green tea, which includes epigallocatechin gallate (EGCG), epicatechin gallate (ECG), epigallocatechin (EGC), and epicatechin (EC), as shown in Fig. 9. Catechins are inexpensive, safe, and can be administered orally. Catechins, especially EGCG, have multifaceted effects that make them attractive candidates for the prevention and treatment of leukemia and myelodysplastic syndrome [92, 93].

Fig. 9
figure 9

The four main active substances of catechins: EC, ECG, EGC, and EGCG

A previous study showed that green tea extract reduced leukocytes and immature cells (progenitor cells) in the peripheral blood, bone marrow, and spleen of leukemic mice while increasing mature cells in the bone marrow. An important observation in leukemic mice is an increase in the number of leukocytes, and treatment with 250 mg/kg green tea extract for 4 days decreased the percentage of leukocytes while decreasing the percentage of immature cells and increasing the percentage of mature cells. These results suggest that green tea extract has anti-leukemic proliferative effects in vivo by inhibiting malignant clonal expansion [94]. In addition, catechins can have anti-leukemic activity by inducing apoptosis. In another study, NB4 cells were inoculated subcutaneously in nude mice, and 10 mM catechin was used as the only drinking water of the mice for 10 days. Tumor size was significantly reduced in the treated group, and no tumor infiltration was detected in any organ at necropsy. The PML-RARα fusion protein was degraded after treatment of primary leukemia cells with 100 and 150 μM catechin for 24 h [93]. This is a strong rationale supporting the therapeutic potential of catechins for APL.

Of the four major catechins, EGCG is the most abundant and potent polyphenolic compound in green tea extract, accounting for 50–75% of total catechins [92]. Due to its long half-life, the compound is rapidly absorbed and distributed in all tissues [93]. EGCG has emerged as an effective inducer of apoptosis through mechanisms involved in caspase activation, regulation of the Bcl-2 family of proteins, disruption of survival signaling pathways, and modulation of redox balance and induction of oxidative stress [92]. It has been shown that EGCG can specifically cause tumor cell death, but it is not toxic to healthy cells. Exposure of HL-60 cells to EGCG reduced cell proliferation and induced apoptosis. When HL-60 cells were treated with EGCG, there was a time-dependent decrease in cell proliferation, and significant induction of apoptosis was seen in EGCG-treated HL-60 cells at day 9 [95]. With the combination of ATRA and EGCG for the treatment of myeloid leukemia, neutrophil differentiation was enhanced. In combination with ATRA, the ATRA-induced effect of DAPK2 activation was enhanced, and granulocyte maturation was enhanced [96]. In addition, as a cell proliferation inhibitor and epigenetic modifier, EGCG may be useful for the treatment of APL [97].

Crude methanolic extract of Mucuna macrocarpa(CMEMM)

Mucuna macrocarpa Wall. (Leguminosae) is a large woody climber that is distributed in China, mainly in Yunnan, Guizhou, Guangdong, Hainan, Guangxi, Taiwan, and Southeast Asia. In folk medicine, the dried stems of this species have been used to enhance blood circulation in a variety of hematological and circulatory disorders [98].

CMEMM in combination with ATO increases the efficacy of ATO [98]. Specifically, HL-60, Jurkat, and Molt-3 cells were treated with 2.5 or 5 μM ATO alone or in combination with increasing doses of CMEMM (25–75 μg/mL). It was found that CMEMM enhanced the growth inhibition of HL-60, Jurkat, and Molt-3 cells after ATO treatment for 24 or 48 h, and combined treatment with ATO and CMEMM synergistically inhibited the growth of HL-60 cells. Additionally, apoptotic morphology and flow cytometry data indicated higher apoptosis induction with combined treatment than with ATO or CMEMM alone. Further studies showed that leukemia cell apoptosis induced by ATO-CMEMM was mediated by oxidative stress [99]. Compared with ATO alone, higher levels of cleaved caspase-3, caspase-9, and poly (ADP-ribose) polymerase were present in HL-60 and Jurkat cells exposed to the ATO-CMEMM combination. In addition, the in vitro antiproliferative effect of 25–75 μg/mL Mucuna macrocarpa on HL-60 cells was dose-dependently and time-dependently enhanced at 72 h. The IC50 of CMEMM was 36.4 μg/mL after 7 h of exposure, and the cells showed apoptotic characteristics. CMEMM (500 mg/kg/day by intraperitoneal injection) inhibited tumor growth in mouse xenografts in vivo. CMEMM exerts its anti-leukemic effect in HL-60 cells through the apoptotic pathway, and it may be considered an anti-leukemic drug candidate in the future.

Discussion

Natural products have good prospects for the treatment of malignant tumors

Nature has always been the natural pharmacy for mankind. Before the advent of modern science and technology, human beings obtained medicines from nature to treat their diseases. The development of modern science and technology is also accompanied by a growing use of traditional medicines worldwide. Natural medicines usually have multiple targets and pathways of action; therefore, they have a variety of biological properties for the treatment of a wide range of diseases, which means that they are often preferred over single-target drugs. In the first two decades of the twentieth century, coronaviruses have ravaged the world several times. Multi-target natural medicines have played an important role in human resistance to coronavirus [100]. Nowadays, although various therapies are emerging for the treatment of malignant tumors, natural medicines are not to be ignored because of mild, safe, and inexpensive.

Natural medicines have good clinical evidence in the treatment of malignant tumors. Paclitaxel, an active ingredient derived from Taxus cuspidata Sieb. Et Zucc., has been widely used in the clinic as a broad-spectrum drug to treat diseases such as breast cancer [101]. In the treatment of hematological malignancies, vincristine, a dimeric indole alkaloid from the leaves of Catharanthus roseus (L.) G. Don, is used in the treatment of acute lymphoblastic leukemia [102], Hodgkin’s lymphoma [103], and other hematological malignancies. Podophyllin is a natural active ingredient derived from the Dysosma species, and its derivative etoposide is a highly active anti-tumor drug, which is used in the treatment of hemophagocytic syndrome [104, 105]. ATO, which is derived from natural products, has become the first-line drug for the treatment of APL worldwide, and the combination of ATO and ATRA can achieve an APL remission rate of 90%. However, this regimen is prone to toxicity and side effects, such as drug resistance, RAS and cardiotoxicity with prolonged use, so it is essential to adopt a combination of drugs for treatment. In addition to oral RIF, which can reduce the cardiotoxicity of arsenicals, natural drugs, such as HKL, CRO, and HHT, can protect the heart when used in combination with ATO. Natural drugs, such as ART, Tan IIA, OA and its derivatives, and fucoidan, amongst others, affect ATRA-resistant cells; therefore, they may be useful therapeutic options in the clinic. In addition to the natural drugs mentioned in this paper, other natural products, such as Acanthopanax senticosus Harms leaf extract [106], Patrinia heterophylla Bunge [107], Korean red ginseng extract [108], and quercetin [109], amongst others, also have therapeutic potential for treating APL, which should be further explored.

Cancer cells are always changing, and they utilize many pathways to resist apoptosis and cell differentiation, which is an important reason for tumor deterioration, drug resistance, and recurrence. Therefore, actively exploring new mechanisms of anti-tumor drugs and developing efficient and low-toxicity therapeutics or adjuvant therapeutic drugs are important steps in the search for new anti-tumor solutions. Natural products are an important source of new drugs and actively exploring the possibilities of natural medicines to treat diseases is just as important as exploring emerging cancer treatment products.

Modern science and technology promote the growth of natural medicines

Since the modern scientific and technological revolution, the development of active ingredients from natural products has increased due to the rapid development of genetic, cell, and fermentation engineering, and drug activities derived from natural products have been continuously explored. Obtaining active ingredients from natural products and developing them into clinical drugs is useful to fully promote the utilization of natural resources.

The potency and content of active ingredients in natural medicines are usually related to their place of origin. Most natural bioactive products face the problem of large-scale production to meet production demand, which constitutes one of the major obstacles for those promising drug candidates to eventually reach the clinic. Natural products with therapeutic activity should have a stable source to meet the marketing demand. For example, HHT is found in plants at extremely low levels, which is a problem that needs to be solved, and only China has achieved profitable production of HHT thus far [43, 44]. To introduce HHT to the world, an alternative source is needed to meet the growing demand. One of the 213 fungal strains isolated from Cephalotaxus hainanensis Li. has the ability to biosynthesize HHT and is expected to provide a sustainable source of HHT [110]. In addition to direct access, chemical synthesis is also a major route for the mass production of natural products. For example, the alkaloidal active ingredient camptothecin, which is derived from Camptotheca acuminata Decne, can either be isolated from the bark of Camptotheca acuminata Decne or synthesized by chemical methods [111]. Although natural products are known to be biologically active, their derivatives can also be actively explored for their biological activities, such as DIOXOL and HIMOXOL, OA derivatives, and etoposide, which is a derivative of podophyllin. In the framework of natural products, changing the chemical groups or chirality may improve therapeutic activity, which is one method of new drug development.

For natural drugs that have been identified to have therapeutic activity but poor oral bioavailability, low solubility, and weak membrane permeability, a number of new delivery technologies can be utilized, including liposomes, solid dispersions, nicotinic aldehyde gels, and nanoliposomes. For example, the oral bioavailability and anti-leukemia activity of Tan IIA can be substantially enhanced using biotinylated lipid bilayer-coated mesoporous silica nanoparticles (Bio-LB-MSNs) as a carrier [112]. Currently, many natural products for the treatment of APL are only at the stage of in vitro study and animal experiments, and they have not yet undergone clinical exploration and translation. Clinical data act as valid evidence for the promotion of natural products. Numerous clinical observations have proven that combined Chinese and Western medicine has value in clinical practice. For example, natural medicines supplemented with chemotherapy can improve the prognosis of patients and enhance their immunity, thus improving the quality of their survival and reducing their medical expenses to a certain extent. Under the premise of safety and effectiveness, natural medicine-related clinical trials should be vigorously promoted for the benefit of a wider group of patients.

Intellectual property protection and promotion of natural medicine

Traditional medicines from China, India, Thailand, and many other countries play important roles in the treatment of diseases. These traditional medicines are not only used to treat diseases, but also they are part of the traditional culture of these countries. The collection of TCMs and traditional prescriptions, the collation and verification of evidence on their use, and the promotion of their application are important for combining Chinese and Western medicines. The Chinese medical community has been tirelessly exploring new medicines in TCM and seeking new applications for existing medicines, instead of completely disregarding traditional remedies or categorizing herbs as food additives. The advancement in our understanding of diseases not only allows for innovation in Western medicine therapy but also creates new possibilities for the “new application of ancient remedies”. Injectable ATO is one of the important achievements of the prescription collection of Chinese tradition. At present, there are still many unknown prescriptions in Chinese folk medicine, and many traditional medicines, including TCMs, have not yet entered the field of intellectual property protection for geographical and linguistic reasons. Traditional prescription provides one source of innovation. Collecting and organizing traditional prescriptions and explaining their mechanisms of action with theories of modern science can recognize the action pathways of natural medicines from different perspectives, and improve the vitality of medical innovation.

The United Nations Convention on Biological Diversity treaty has included the protection of traditional medicinal knowledge within its framework, and the efforts of international organizations have led some developed countries to pay attention to the protection of traditional medicinal knowledge and to implement specific rules with the help of existing intellectual property rights protection. At present, there is no law specifically protecting traditional medicine knowledge in China, and the protection methods are scattered. None of the existing intellectual property laws can systematically locate and comprehensively protect traditional medicine knowledge. Moreover, due to the scattered provisions, the protection effect is relatively weak and the scope of protection is narrow [113]. Developers from economically developed countries and regions rely on their scientific and technological knowledge to develop, utilize, improve, and innovate traditional medicine without permission. They use the evidence acquired from these investigations to develop new medicines and obtain intellectual property rights, mainly patents, as well as to obtain high commercial profits, resulting in the frequent loss of intellectual property rights of TCM, which is already faced with a lack of protection [114]. As a successful country in protecting traditional medicines, India has gradually established a unique intellectual property system to regulate the traditional medicine industry, while resisting biopiracy [115]. This is a good example that the development of natural products should be based on the protection of origin and intellectual property. The development of natural medicine should conducted on the premise of mutual benefit, and ultimately benefit for the world.

Availability of data and materials

The datasets presented in this review can be found in online repositories.

Abbreviations

WHO:

World Health Organization

APL:

Acute promyelocytic leukemia

AML:

Acute myeloid leukemia

PML:

Promyelocytic leukemia

RARα:

Retinoic acid receptor-α

CR:

Complete remission

ATRA:

All-trans retinoic

ATO:

Arsenic trioxide

TCM:

Traditional Chinese medicine

RIF:

Realgar-indigo naturalis formula

HHT:

Homoharringtonine

DFS:

Disease-free survival

Ara-C:

CytosineArabinoside

DNR:

Daunorubicin

IDA:

Idarubicin

RAS:

Retinoic acid syndrome

HKL:

Honokiol

MAG:

Magnolol

ROS:

Reactive oxygen species

DL:

Dehydrocostus lactone

ART:

Artesunate

ALT:

Alanine transaminase

AST:

Aspartate transaminase

BUN:

Blood urea nitrogen

CREA:

Creatinine concentrations

Tan IIA:

Tanshinone IIA

OA:

Oleanolic acid

UA:

Ursolic acid

NF-κB:

Nuclear factor kappa-B

CRO:

Crocin

CRT:

Crocetin

EGCG:

Epigallocatechin gallate

ECG:

Epicatechin gallate

EGC:

Epigallocatechin

EC:

Epicatechin

CMEMM:

Crude methanolic extract of Mucuna macrocarpa

References

  1. Sung H, Ferlay J, Siegel RL, Laversanne M, Soerjomataram I, Jemal A, et al. Global Cancer Statistics 2020: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries. CA Cancer J Clin. 2021;71(3):209–49. https://doi.org/10.3322/caac.21660.

    Article  PubMed  Google Scholar 

  2. Hillestad LK. Acute promyelocytc leukemia. J Intern Med. 1957;159(3):189–94. https://doi.org/10.1111/j.0954-6820.1957.tb00124.x.

    Article  CAS  Google Scholar 

  3. Shen Z, Huang X, Ma J. Chinese guidelinesfor diagnosisand treatment of acute promyelocytic leukemia (2018). Chin J Hematol. 2018;39(3):179–83. https://doi.org/10.3760/cma.j.issn.0253-3737.2018.03.002.

    Article  Google Scholar 

  4. He C, Yu J. Progress of compound huangdai tablets in the treatment of acute promyelocytic leukemia in children. J Pediatr Pharm. 2022;28(8):54–7.

    CAS  Google Scholar 

  5. Zhang X, Guo X. Risk factors of thrombosis in Chinese subjects with acute promyelocytic leukemia. Thrombosis J. 2021;19(1):42. https://doi.org/10.1186/s12959-021-00294-7.

    Article  CAS  Google Scholar 

  6. Zhang T. The development of arsenic. Chin J Integr Tradit West Med. 2001;23(1):65–6.

    Google Scholar 

  7. Chen Z, Chen G, Zhang T, Wang Z, Chen S. Treatment of acute promyelocytic leukemia with traditional Chinese medicine and induced cell differentiation and apoptosis. Collected abstracts of papers from the World Integrative Medicine Congress, Beijing: 1997, p. 47.

  8. Coombs CC, Tavakkoli M, Tallman MS. Acute promyelocytic leukemia: where did we start, where are we now, and the future. Blood Cancer J. 2015;5(4):e304–e304. https://doi.org/10.1038/bcj.2015.25.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  9. Sanz MA, Grimwade D, Tallman MS, Lowenberg B, Fenaux P, Estey EH, et al. Management of acute promyelocytic leukemia: recommendations from an expert panel on behalf of the European LeukemiaNet. Blood. 2009;113(9):1875–91. https://doi.org/10.1182/blood-2008-04-150250.

    Article  CAS  PubMed  Google Scholar 

  10. Huang X. Chinese guideline for diagnosis and treatment of promyelocytic leukemia (2014): shine Chinese characteristic guideline template. Chin J Hematol. 2014;35(5):387. https://doi.org/10.3760/cma.j.issn.025-2727.2014.05.002.

    Article  Google Scholar 

  11. Pollyea DA, Altman JK, Bixby D, Fathi A. Acute myeloid leukemia, version 3.2023, NCCN clinical practice guidelines in oncology. J Natl Compr Cancer Netw. 2023. https://doi.org/10.6004/jnccn.2023.0025.

    Article  Google Scholar 

  12. Sanz MA, Fenaux P, Tallman MS, Estey EH, Löwenberg B, Naoe T, et al. Management of acute promyelocytic leukemia: updated recommendations from an expert panel of the European LeukemiaNet. Blood. 2019;133(15):1630–43. https://doi.org/10.1182/blood-2019-01-894980.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  13. Kayser S, Schlenk RF, Platzbecker U. Management of patients with acute promyelocytic leukemia. Leukemia. 2018;32(6):1277–94. https://doi.org/10.1038/s41375-018-0139-4.

    Article  PubMed  Google Scholar 

  14. Sun H, Ma L, Hu X, Zhang T, Rong F, Wang X, et al. Report on 16 cases of long term survival of acute promyelocytic leukemia with combination of ailing no.1 and traditional Chinese medicine diagnosis and treatment. Inf Tradit Chin Med. 1991;6:39–41. https://doi.org/10.19656/j.cnki.1002-2406.1991.06.018.

    Article  Google Scholar 

  15. Hu X, Liu F, Ma R, Deng C. Zhou Aixiang’s experience in treating leukemia with Qinghuang powder. J Tradit Chin Med. 2011;52(14):1187–9. https://doi.org/10.13288/j.11-2166/r.2011.14/007.

    Article  Google Scholar 

  16. Li L, Liu X. Observation on the therapeutic effect of dialectical treatment for 59 cases of leukemia. Hebei J Tradit Chin Med. 1995;17(2):10–1.

    Google Scholar 

  17. Xie L. Treatment of acute leukemia with severe infection by tongfu xiehe method combined with antibiotics. Hunan J Tradit Chin Med. 1993;9(05):55. https://doi.org/10.16808/j.cnki.issn1003-7705.1993.05.044.

    Article  Google Scholar 

  18. Chen G, Zhu J, Shi X, Ni J, Zhong H, Jin X, et al. In vitro studies on cellular and molecular mechanisms of arsenic trioxide (As2O3) in the treatment of acute promyelocytic leukemia: As2O3 induces NB4 cell apoptosis with downregulation of Bcl-2 expression and modulation of PML-RARα/PML proteins. Blood. 1996;88(3):1052–61. https://doi.org/10.1182/blood.V88.3.1052.1052.

    Article  CAS  PubMed  Google Scholar 

  19. Luo X, Jiang H. Chinese guideline for diagnosis and treatment of childhood acute promyelocytic leukemia. Chin J Appl Clin Pediatr. 2022;37(2):81–8. https://doi.org/10.3760/cma.j.cn101070-20211103-01309.

    Article  Google Scholar 

  20. Ma J. Chinses guidelines for diagnosis and treatment of acute promyelocytic leukemia (2014). Chin J Hematol. 2014;35(3):475–7. https://doi.org/10.3760/cma.j.issn.0253-2727.2014.05.024.

    Article  CAS  Google Scholar 

  21. Yang Z, Wang X, Zhang L, Cheng J, Wang Y, Hou L. Research progress in homoharringtonine. Drug Eval Res. 2019;42(7):781–6. https://doi.org/10.7501/j.issn.1674-6376.2019.04.035.

    Article  Google Scholar 

  22. Wang J, Liu Y, Hu J, Chen C. Potential of natural products in combination with arsenic trioxide: investigating cardioprotective effects and mechanisms. Biomed Pharmacother. 2023;162:114464. https://doi.org/10.1016/j.biopha.2023.114464.

    Article  CAS  PubMed  Google Scholar 

  23. Goel H, Kumar R, Tanwar P, Upadhyay TK, Khan F, Pandey P, et al. Unraveling the therapeutic potential of natural products in the prevention and treatment of leukemia. Biomed Pharmacother. 2023;160:114351. https://doi.org/10.1016/j.biopha.2023.114351.

    Article  CAS  PubMed  Google Scholar 

  24. Cotoraci C, Ciceu A, Sasu A, Miutescu E, Hermenean A. The anti-leukemic activity of natural compounds. Molecules. 2021;26(9):2709. https://doi.org/10.3390/molecules26092709.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  25. Englinger B, Pirker C, Heffeter P, Terenzi A, Kowol CR, Keppler BK, et al. Metal drugs and the anticancer immune response. Chem Rev. 2019;119(2):1519–624. https://doi.org/10.1021/acs.chemrev.8b00396.

    Article  CAS  PubMed  Google Scholar 

  26. Shen X, Gao K, Sui M, Zhang Z. Progress in long-term survival of patients with acute promyelocytic leukemia treated with arsenite acid. Mod Oncol. 2023;31(02):360–3. https://doi.org/10.3969/j.issn.1672-4992.2023.02.032.

    Article  Google Scholar 

  27. Zhang T. Arsenite injection was born in China. Compilation of papers of the first International Conference on Rheumatology of Integrated Chinese and Western Medicine, Harbin: 2004.

  28. Kantarjian H, Kadia T, DiNardo C, Daver N, Borthakur G, Jabbour E, et al. Acute myeloid leukemia: current progress and future directions. Blood Cancer J. 2021;11(2):41. https://doi.org/10.1038/s41408-021-00425-3.

    Article  PubMed  PubMed Central  Google Scholar 

  29. Chen L, Zhu H, Li Y, Liu Q, Hu Y, Zhou J, et al. Arsenic trioxide replacing or reducing chemotherapy in consolidation therapy for acute promyelocytic leukemia (APL2012 trial). Proc Natl Acad Sci USA. 2021;118(6): e2020382118. https://doi.org/10.1073/pnas.2020382118.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  30. Platzbecker U, Avvisati G, Cicconi L, Thiede C, Paoloni F, Vignetti M, et al. Improved outcomes with retinoic acid and arsenic trioxide compared with retinoic acid and chemotherapy in non–high-risk acute promyelocytic leukemia: final results of the randomized Italian-German APL0406 Trial. J Clin Oncol. 2017;35(6):605–12. https://doi.org/10.1200/JCO.2016.67.1982.

    Article  CAS  PubMed  Google Scholar 

  31. World Health Organization. Arsenic, www.who.int/news-room/fact-sheets/detail/arsenic;2023. Accessed 17 Dec 2023.

  32. Fujisawa S, Ohno R, Shigeno K, Sahara N, Nakamura S, Naito K, et al. Pharmacokinetics of arsenic species in Japanese patients with relapsed or refractory acute promyelocytic leukemia treated with arsenic trioxide. Cancer Chemother Pharmacol. 2007;59(4):485–93. https://doi.org/10.1007/s00280-006-0288-4.

    Article  CAS  PubMed  Google Scholar 

  33. Zhu H, Hu J, Lo-Coco F, Jin J. The simpler, the better: oral arsenic for acute promyelocytic leukemia. Blood. 2019;134(7):597–605. https://doi.org/10.1182/blood.2019000760.

    Article  CAS  PubMed  Google Scholar 

  34. Kumana CR, Kwong Y, Gill H. Oral arsenic trioxide for treating acute promyelocytic leukaemia: Implications for its worldwide epidemiology and beyond. Front Oncol. 2022;12:1026478. https://doi.org/10.3389/fonc.2022.1026478.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  35. Siu C, Au W, Yung C, Kumana CR, Lau C, Kwong Y, et al. Effects of oral arsenic trioxide therapy on QT intervals in patients with acute promyelocytic leukemia: implications for long-term cardiac safety. Blood. 2006;108(1):103–6. https://doi.org/10.1182/blood-2006-01-0054.

    Article  CAS  PubMed  Google Scholar 

  36. Chen N. HUANG Shilin’s experience in the treatment of acute promyelocytic leukemia. J Tradit Chin Med. 2016;57:1185–7. https://doi.org/10.13288/j.11-2166/r.2016.14.004.

    Article  Google Scholar 

  37. Bai Y, Huang S. Studies on red orpiment induction of NB4 and HL-60cell apoptosis. Chin J Hematol. 1998;19(9):477–80.

    CAS  Google Scholar 

  38. Wang G, Zhou L, Wang L. The advances of active composition of natural medicine to leukemia cells apoptosis. Nat Prod Res Dev. 2004;16(3):269–72. https://doi.org/10.16333/j.1001-6880.2004.03.025.

    Article  CAS  Google Scholar 

  39. Li G, Li R, Pan Y, Ma W, Liu Y, Xu J, et al. The adverse reactions of arsenic in the treatment of acute promyelocytic leukemia and the prevention and treatment of traditional Chinese medicine. Beijing J Tradit Chin Med. 2022;41(8):930–4.

    Google Scholar 

  40. Yang M, Wan W, Luo J, Zheng M, Huang K, Yang L, et al. Multicenter randomized trial of arsenic trioxide and Realgar- Indigo naturalis formula in pediatric patients with acute promyelocytic leukemia: Interim results of the SCCLG-APL clinical study. Am J Hematol. 2018;93(12):1467–73. https://doi.org/10.1002/ajh.25271.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  41. Zhu H, Wu D, Du X, Zhang X, Liu L, Ma J, et al. Oral arsenic plus retinoic acid versus intravenous arsenic plus retinoic acid for non-high-risk acute promyelocytic leukaemia: a non-inferiority, randomised phase 3 trial. Lancet Oncol. 2018;19(7):871–9. https://doi.org/10.1016/S1470-2045(18)30295-X.

    Article  CAS  PubMed  Google Scholar 

  42. Lou Y, Ma Y, Jin J, Zhu H. Oral realgar-indigo naturalis formula plus retinoic acid for acute promyelocytic leukemia. Front Oncol. 2021;10:597601. https://doi.org/10.3389/fonc.2020.597601.

    Article  PubMed  PubMed Central  Google Scholar 

  43. Lu D, Cao J, Xu B. Biological activities and clinical utilizations of harringtonine and homoharringtonine. Nat Prod Res Dev. 2000;12(5):70–3. https://doi.org/10.3969/j.issn.1001-6880.2000.05.017.

    Article  CAS  Google Scholar 

  44. Xia X, Xia G, Wu Y, Xia H, Wang L, Shang H, et al. Trace therapeutic substances of traditional Chinese medicine: great resources of innovative drugs derived from traditional Chinese medicine. China J Chin Mater Med. 2022;47(7):1705–29. https://doi.org/10.19540/j.cnki.cjcmm.20220210.201.

    Article  Google Scholar 

  45. Wang Y, Liu B, Wei H, Lin D, Zhou C, Liu K, et al. Homoharringtonine in newly diagnosed acute promyelocytic leukemia treatment: a prospective, randomized controlled trial. Chin J Hematol. 2016;37(3):183–8. https://doi.org/10.3760/cma.j.issn.0253-2727.2016.03.002.

    Article  CAS  Google Scholar 

  46. Yuan Y, Li W, Lin D, Mi Y, Wang Y, Wei H, et al. Outcome of acute promyelocytic leukemia with homoharringtonine and ATRA. Chin J Hematol. 2011;32(11):752–7. https://doi.org/10.3760/cma.j.issn.0253-2727.2011.11.007.

    Article  Google Scholar 

  47. Bian S, Wang Z, Hao Y, Yan W, Yang T, Qian L, et al. Combination Chemotherapv for acute non-lumphoblastic leukemias in adult. A conparison of HAT AND D (A) AT protocols. Chin J Hematol. 1988;9(8):449–52. https://doi.org/10.3760/cma.j.issn.0253-2727.1988.08.101.

    Article  Google Scholar 

  48. Li Y. Study of Homoharringtonine and daunorubicin in acute promyelocytic leukemia. Guide Chin Med. 2020;18(1):147–8. https://doi.org/10.15912/j.cnki.gocm.2020.01.125.

    Article  Google Scholar 

  49. Wang Y, Lin D, Wei H, Li W, Liu B, Zhou C, et al. Long-term follow-up of homoharringtonine plus all-trans retinoic acid-based induction and consolidation therapy in newly diagnosed acute promyelocytic leukemia. Int J Hematol. 2015;101(3):279–85. https://doi.org/10.1007/s12185-014-1730-8.

    Article  CAS  PubMed  Google Scholar 

  50. Pei R, Li S, Zhang P, Ma J, Liu X, Du X, et al. Clinical investigation of homoharringtonine in combination with all transretinoic acid and arsenic trioxide for acute promyelocytic leukemia. Chin J Hematol. 2013;34(2):144–8. https://doi.org/10.3760/cma.j.issn.0253-2727.2013.02.012.

    Article  Google Scholar 

  51. Bennett MT, Sirrs S, Yeung JK, Smith CA. Hypercalcemia due to all trans retinoic acid in the treatment of acute promyelocytic leukemia potentiated by voriconazole. Leuk Lymphoma. 2005;46(12):1829–31. https://doi.org/10.1080/10428190500235298.

    Article  CAS  PubMed  Google Scholar 

  52. Rauf A, Olatunde A, Imran M, Alhumaydhi FA, Aljohani ASM, Khan SA, et al. Honokiol: a review of its pharmacological potential and therapeutic insights. Phytomedicine. 2021;90:153647. https://doi.org/10.1016/j.phymed.2021.153647.

    Article  CAS  PubMed  Google Scholar 

  53. Sarrica A, Kirika N, Romeo M, Salmona M, Diomede L. Safety and toxicology of magnolol and honokiol. Planta Med. 2018;84(16):1151–64. https://doi.org/10.1055/a-0642-1966.

    Article  CAS  PubMed  Google Scholar 

  54. Liu X, Gu Y, Bian Y, Cai D, Li Y, Zhao Y, et al. Honokiol induces paraptosis-like cell death of acute promyelocytic leukemia via mTOR and MAPK signaling pathways activation. Apoptosis. 2021;26(3–4):195–208. https://doi.org/10.1007/s10495-020-01655-9.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  55. Xue F, Cheng Z, Liang W, Chen H, Wang S, Yao L, et al. Resistance reverse effect of honokiol on multidrug resistance of U937/ADR cell line. J Shanghai Jiaotong Univ (Med Sci). 2009;29(9):1035–9. https://doi.org/10.1360/972009-495.

    Article  CAS  Google Scholar 

  56. Li S. The effect of honokiol combiend with cytarbine on human acute myeloid leukemia and the study of its mechanism. Doctoral dissertation. Zhejiang University, 2014.

  57. Huang A, Yang F, Cheng P, Liao D, Zhou L, Ji X, et al. Honokiol attenuate the arsenic trioxide-induced cardiotoxicity by reducing the myocardial apoptosis. Pharmacol Res Perspec. 2022;10(2): e00914. https://doi.org/10.1002/prp2.914.

    Article  CAS  Google Scholar 

  58. Lin J, Chen S. Advance in antitumor activity and mechanism of natural sesquiterpene lactones. Cent South Pharm. 2023;21(6):1589–98. https://doi.org/10.7539/j.issn.1672-2981.2023.06.029.

    Article  Google Scholar 

  59. Oh G, Pae H, Chung H, Kwon J, Lee J, Kwon T, et al. Dehydrocostus lactone enhances tumor necrosis factor-α-induced apoptosis of human leukemia HL-60 cells. Immunopharmacol Immunotoxicol. 2004;26(2):163–75. https://doi.org/10.1081/IPH-120037712.

    Article  CAS  PubMed  Google Scholar 

  60. Roozbehani M, Abdolmohammadi MH, Hamzeloo-Moghadam M, Irani S, Fallahian F. Gaillardin, a potent sesquiterpene lactone induces apoptosis via down-regulation of NF-κβ in gastric cancer cells, AGS and MKN45. J Ethnopharmacol. 2021;281:114529. https://doi.org/10.1016/j.jep.2021.114529.

    Article  CAS  PubMed  Google Scholar 

  61. Cao F, Chu C, Qin J, Guan X. Research progress on antitumor mechanisms and molecular targets of Inula sesquiterpene lactones. Chin Med. 2023;18:164. https://doi.org/10.1186/s13020-023-00870-1.

    Article  PubMed  PubMed Central  Google Scholar 

  62. Yang L, Wang X, Hou A, Zhang J, Wang S, Man W, et al. A review of the botany, traditional uses, phytochemistry, and pharmacology of the Flos Inulae. J Ethnopharmacol. 2021;276:114125. https://doi.org/10.1016/j.jep.2021.114125.

    Article  CAS  PubMed  Google Scholar 

  63. Karami A, Hamzeloo-Moghadam M, Yami A, Barzegar M, Mashati P, Gharehbaghian A. Antiproliferative effect of gaillardin from Inula oculus-christi in human leukemic cells. Nutr Cancer. 2020;72(6):1043–56. https://doi.org/10.1080/01635581.2019.1665188.

    Article  CAS  PubMed  Google Scholar 

  64. Sayyadi M, Moradabadi A, Noroozi-Aghideh A, Yazdanian M. Effect of gaillardin on proliferation and apoptosis of acute promyelocytic leukemia cell lines, NB4 as cancer treatment. Biointerface Res Appl Chem. 2020;11(1):7445–52. https://doi.org/10.33263/BRIAC111.74457452.

    Article  Google Scholar 

  65. Jiang Y, Dong Y, Zhou F, Chen J, Zhou Y, Tian C, et al. Research progress on artemisinin and its derivatives. Chin Tradit Herb Drugs. 2022;53(2):599–608. https://doi.org/10.7501/j.issn.0253-2670.2022.02.030.

    Article  Google Scholar 

  66. Steinbrück L, Pereira G, Efferth T. Effects of artesunate on cytokinesis and G2/M cell cycle progression of tumour cells and budding yeast. Cancer Genom Proteom. 2010;7(6):337–46.

    Google Scholar 

  67. Zhuang Y. Experimental study of Puerariae radix flavone and Artesunate against Acute promyelocytic Leukemia Cells in vitro. Doctoral dissertation. Nanjing University of Chinese Medicine, 2018.

  68. Wang C, Dai S, Zhao X, Zhang Y, Gong L, Fu K, et al. Celastrol as an emerging anticancer agent: current status, challenges and therapeutic strategies. Biomed Pharmacother. 2023;163:114882. https://doi.org/10.1016/j.biopha.2023.114882.

    Article  CAS  PubMed  Google Scholar 

  69. Uttarkar S, Dassé E, Coulibaly A, Steinmann S, Jakobs A, Schomburg C, et al. Targeting acute myeloid leukemia with a small molecule inhibitor of the Myb/p300 interaction. Blood. 2016;127(9):1173–82. https://doi.org/10.1182/blood-2015-09-668632.

    Article  CAS  PubMed  Google Scholar 

  70. Zhang X, Yang J, Chen M, Li L, Huan F, Li A, et al. Metabolomics profiles delineate uridine deficiency contributes to mitochondria-mediated apoptosis induced by celastrol in human acute promyelocytic leukemia cells. Oncotarget. 2016;7(29):46557–72. https://doi.org/10.18632/oncotarget.10286.

    Article  PubMed  PubMed Central  Google Scholar 

  71. Cao Y, Wang S, Li X, Zhang Y, Qiao Y. The anticancer mechanism investigation of Tanshinone IIA by pharmacological clustering in protein network. BMC Syst Biol. 2018;12(1):90. https://doi.org/10.1186/s12918-018-0606-6.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  72. Li J, Zhang K, Yang Y, Meng W. Tanshinone IIA in acute promyelocytic leukemia. Am J Med Sci. 2012;344(4):283–8. https://doi.org/10.1097/MAJ.0b013e318240bca6.

    Article  PubMed  Google Scholar 

  73. Guo Q. In vitro study on the differentiation mechanism of NB4 cells induced by tanshinoneIIA and comparative study with ATRA and As2O3. Doctoral dissertation. Zhengzhou University, 2013.

  74. Wang D, Ding Y, Chen J, You H, Wei L, Xu Y, et al. TanshinoneIIA induces autophagy via PI3K/Akt /mTOR signaling pathway in human leukemia NB4 cell line in vitro. J China Pediatr Blood Cancer. 2020;25(1):4–8. https://doi.org/10.3969/j.ossn.1673-5323.2020.01.002.

    Article  CAS  Google Scholar 

  75. Wang D. Chemotherapy sensitizing effect of Tan IIA combined with ATO on acute promyelocyte leukemia and its mechanism in vivo and in vitro. Doctoral dissertation. Zhengzhou University, 2015.

  76. Yang Y, Liu T. Complete remission of acute promyelocytic leukemia resisting all trans retinoic acid of one case treated by TanshinoneIIA. J Sichuan Univ (Med Sci Edi). 2006;37(6):965–7.

    Google Scholar 

  77. Liang Y, Song W, Wang J, Jing L, Qu W, Fu R, et al. A study on the cell differentiation induced by tanshinone II A and its molecular mechanism in retinotic acid: resistant acute promyelocytic leukemia. Chin J Intern Med. 2005;44(5):366–9. https://doi.org/10.3760/j.issn:0578-1426.2005.05.015.

    Article  CAS  Google Scholar 

  78. Castellano JM, Ramos-Romero S, Perona JS. Oleanolic acid: extraction, characterization and biological activity. Nutr. 2022;14(3):623. https://doi.org/10.3390/nu14030623.

    Article  CAS  Google Scholar 

  79. Patlolla JMR, Rao CV. Triterpenoids for cancer prevention and treatment: current status and future prospects. Curr Pharm Biotechnol. 2012;13(1):147–55. https://doi.org/10.2174/138920112798868719.

    Article  CAS  PubMed  Google Scholar 

  80. Rawendra RDS, Lin P, Chang C, Hsu J, Huang T, Shih W. Potentiation of acute promyelocytic leukemia cell differentiation and prevention of leukemia development in mice by oleanolic acid. Anticancer Res. 2015;35(12):6583–90.

    CAS  PubMed  Google Scholar 

  81. Paszel-Jaworska A, Rubiś B, Bednarczyk-Cwynar B, Zaprutko L, Rybczyńska M. Proapoptotic activity and ABCC1-related multidrug resistance reduction ability of semisynthetic oleanolic acid derivatives DIOXOL and HIMOXOL in human acute promyelocytic leukemia cells. Chem-Biol Interact. 2015;242:1–12. https://doi.org/10.1016/j.cbi.2015.07.011.

    Article  CAS  PubMed  Google Scholar 

  82. Black WAP. The seasonal variation in the combined L-fucose content of the common British Laminariaceae and fucaceae. J Sci Food Agric. 1954;5(9):445–8. https://doi.org/10.1002/jsfa.2740050909.

    Article  CAS  Google Scholar 

  83. Fitton, Stringer, Park, Karpiniec. Therapies from Fucoidan: new developments. Mar Drugs. 2019;17(10):571. https://doi.org/10.3390/md17100571.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  84. Atashrazm F, Lowenthal RM, Woods GM, Holloway AF, Karpiniec SS, Dickinson JL. Fucoidan suppresses the growth of human acute promyelocytic leukemia cells in vitro and In Vivo. J Cell Physiol. 2016;231(3):688–97. https://doi.org/10.1002/jcp.25119.

    Article  CAS  PubMed  Google Scholar 

  85. Atashrazm F, Lowenthal RM, Dickinson JL, Holloway AF, Woods GM. Fucoidan enhances the therapeutic potential of arsenic trioxide and all-trans retinoic acid in acute promyelocytic leukemia, in vitro and in vivo. Oncotarget. 2016;7(29):46028–41. https://doi.org/10.18632/oncotarget.10016.

    Article  PubMed  PubMed Central  Google Scholar 

  86. Lian H, Hurilebagen HQ. A Review of crocin and crocetin in the Saffron. J Med Pharm Chin Minor. 2021;27(8):53–7. https://doi.org/10.16041/j.cnki.cn15-1175.2021.08.025.

    Article  Google Scholar 

  87. Lv M, Wang Q, Yang S, Chen L. Research progress of saffron and its components in inhibiting the expression of inflammatory factors. Chongqing Med. 2017;46(13):1850–3.

    Google Scholar 

  88. Bakshi H, Sam S, Rozati R, Sultan P, Rathore B, Lone Z, et al. DNA fragmentation and cell cycle arrest: a hallmark of apoptosis induced by crocin from kashmiri saffron in a human pancreatic cancer cell line. Asian Pac J Cancer Prev. 2010;11(3):675–9. https://doi.org/10.1186/ar2982.

    Article  CAS  PubMed  Google Scholar 

  89. Sun Y, Xu H, Zhao Y, Wang L, Sun L, Wang Z, et al. Crocin exhibits antitumor effects on human leukemia HL-60 cells in vitro and in vivo. Evid-Based Complement Altern Med. 2013;2013:1–7. https://doi.org/10.1155/2013/690164.

    Article  Google Scholar 

  90. Liang Y, Zheng B, Li J, Shi J, Chu L, Han X, et al. Crocin ameliorates arsenic trioxide-induced cardiotoxicity via Keap1-Nrf2/HO-1 pathway: reducing oxidative stress, inflammation, and apoptosis. Biomed Pharmacother. 2020;131:110713. https://doi.org/10.1016/j.biopha.2020.110713.

    Article  CAS  PubMed  Google Scholar 

  91. Liu P, Xue Y, Zheng B, Liang Y, Zhang J, Shi J, et al. Crocetin attenuates the oxidative stress, inflammation and apoptosis in arsenic trioxide-induced nephrotoxic rats: implication of PI3K/AKT pathway. Int Immunopharmacol. 2020;88:106959. https://doi.org/10.1016/j.intimp.2020.106959.

    Article  CAS  PubMed  Google Scholar 

  92. Della Via FI, Alvarez MC, Basting RT, Saad STO. The effects of green tea catechins in hematological malignancies. Pharm. 2023;16(7):1021. https://doi.org/10.3390/ph16071021.

    Article  CAS  Google Scholar 

  93. Zhang L, Chen Q, Xu P, Qian Y, Wang A, Xiao D, et al. Catechins induced acute promyelocytic leukemia cell apoptosis and triggered PML-RARα oncoprotein degradation. J Hematol Oncol. 2014;7(1):75. https://doi.org/10.1186/s13045-014-0075-3.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  94. Torello CO, Shiraishi RN, Della Via FI, Castro TCLD, Longhini AL, Santos I, et al. Reactive oxygen species production triggers green tea-induced anti-leukaemic effects on acute promyelocytic leukaemia model. Cancer Lett. 2018;414:116–26. https://doi.org/10.1016/j.canlet.2017.11.006.

    Article  CAS  PubMed  Google Scholar 

  95. Berletch JB, Liu C, Love WK, Andrews LG, Katiyar SK, Tollefsbol TO. Epigenetic and genetic mechanisms contribute to telomerase inhibition by EGCG. J Cell Biochem. 2008;103(2):509–19. https://doi.org/10.1002/jcb.21417.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  96. Britschgi A, Simon H, Tobler A, Fey MF, Tschan MP. Epigallocatechin-3-gallate induces cell death in acute myeloid leukaemia cells and supports all- trans retinoic acid-induced neutrophil differentiation via death-associated protein kinase 2. Br J Haematol. 2010;149(1):55–64. https://doi.org/10.1111/j.1365-2141.2009.08040.x.

    Article  CAS  PubMed  Google Scholar 

  97. Borutinskaitė V, Virkšaitė A, Gudelytė G, Navakauskienė R. Green tea polyphenol EGCG causes anti-cancerous epigenetic modulations in acute promyelocytic leukemia cells. Leuk Lymphoma. 2018;59(2):469–78. https://doi.org/10.1080/10428194.2017.1339881.

    Article  CAS  PubMed  Google Scholar 

  98. Lu K, Lee H, Huang M, Lai S, Ho Y, Chang Y, et al. Synergistic apoptosis-inducing Antileukemic effects of arsenic trioxide and Mucuna macrocarpa stem extract in human leukemic cells via a reactive oxygen species-dependent mechanism. Evid-Based Complement Altern Med. 2012;2012:1–14. https://doi.org/10.1155/2012/921430.

    Article  Google Scholar 

  99. Lu K, Chang Y, Yin P, Chen T, Ho Y, Chang Y, et al. In vitro and in vivo apoptosis-inducing antileukemic effects of Mucuna macrocarpa Stem extract on HL-60 human leukemia cells. Integr Cancer Ther. 2010;9(3):298–308. https://doi.org/10.1177/1534735410378661.

    Article  CAS  PubMed  Google Scholar 

  100. Chen J, Ding Z. Advances in natural product anti-coronavirus research (2002–2022). Chin Med. 2023;18:13. https://doi.org/10.1186/s13020-023-00715-x.

    Article  PubMed  PubMed Central  Google Scholar 

  101. Chinese Anti-Cancer Association, Committee of Breast Cancer Society. Guideline for Breast Cancer of Chinese Anti-cancer Association (2021 edition). Chin Oncol. 2021;31(10):954–1040. https://doi.org/10.19401/j.cnki.1007-3639.2021.10.013

  102. Qiu L, Wang J. Chinese guidelines for diagnosis and treatment of adult acute lymphoblastic leukemia (2021). Chin J Hematol. 2021;42(9):705–16. https://doi.org/10.3760/cma.j.issn.0253-2727.2021.09.001.

    Article  Google Scholar 

  103. Cai Q, Li J, Qiu L. The guidelines for diagnosis and treatment of Hodgkin lymphoma in China (2022). Chin J Hematol. 2022;43(9):705–15. https://doi.org/10.3760/cma.j.issn.0253-2727.2022.09.001.

    Article  Google Scholar 

  104. Zhu C, Yang J, Li D, Zhao L, Pan X, Xiong Y. Research progress of natural antitumor drug Podophyllotoxin and its derivatives. Drug Eval. 2004;1(4):306–9. https://doi.org/10.3969/j.issn.1672-2809.2004.04.014.

    Article  Google Scholar 

  105. Wang Z, Wang T. Chinese Guidelines for Diagnosis and Treatment of hemophagocytic syndrome (2022 edition). Natl Med J China. 2022;102(20):1492–9. https://doi.org/10.3760/cma.j.cn112137-20220310-00488.

    Article  Google Scholar 

  106. Han Y, Zhang A, Zhang Y, Sun H, Meng X, Wang X. Chemical metabolomics for investigating the protective effectiveness of Acanthopanax senticosus Harms leaf against acute promyelocytic leukemia. RSC Adv. 2018;8(22):11983–90. https://doi.org/10.1039/C8RA01029C.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  107. Feng L, Zhu S, Ma J, Hong Y, Wan M, Qiu Q, et al. Integrated bioinformatics analysis and network pharmacology to explore the potential mechanism of Patrinia heterophylla Bunge against acute promyelocytic leukemia. Med. 2023;102(40): e35151. https://doi.org/10.1097/MD.0000000000035151.

    Article  CAS  Google Scholar 

  108. Jo S, Lee H, Kim S, Lee CH, Chung H. Korean red ginseng extract induces proliferation to differentiation transition of human acute promyelocytic leukemia cells via MYC-SKP2-CDKN1B axis. J Ethnopharmacol. 2013;150(2):700–7. https://doi.org/10.1016/j.jep.2013.09.036.

    Article  CAS  PubMed  Google Scholar 

  109. Ramos AM, Aller P. Quercetin decreases intracellular GSH content and potentiates the apoptotic action of the antileukemic drug arsenic trioxide in human leukemia cell lines. Biochem Pharmacol. 2008;75(10):1912–23. https://doi.org/10.1016/j.bcp.2008.02.007.

    Article  CAS  PubMed  Google Scholar 

  110. Hu X, Li W, Yuan M, Li C, Liu S, Jiang C, et al. Homoharringtonine production by endophytic fungus isolated from Cephalotaxus hainanensis Li. World J Microbiol Biotechnol. 2016;32(7):110. https://doi.org/10.1007/s11274-016-2073-9.

    Article  CAS  PubMed  Google Scholar 

  111. Feng J, Zhang Y, Tan Y, Zhang W. The development in research on Camptotheca acuminata and utilization of camptothecin. Sci Silvae Sin. 2000;36(5):100–8.

    Google Scholar 

  112. Li Z, Zhang Y, Zhang K, Wu Z, Feng N. Biotinylated-lipid bilayer coated mesoporous silica nanoparticles for improving the bioavailability and anti-leukaemia activity of Tanshinone IIA. Artif Cells Nanomed Biotechnol. 2018;46(1):578–87. https://doi.org/10.1080/21691401.2018.1431651.

    Article  CAS  PubMed  Google Scholar 

  113. Ma X. The breakthrough of protection of traditional medicine intellectual property right and the innovation of China. Guizhou Ethn Stud. 2022;43(01):79–85. https://doi.org/10.13965/j.cnki.gzmzyj10026959.2022.01.011.

    Article  Google Scholar 

  114. Chen X. Research on the protection of intellectual property rights of traditional medicine. People’s Trib. 2015. https://doi.org/10.16619/j.cnki.rmlt.2015.32.061.

    Article  Google Scholar 

  115. Hu J. Analyses the enlightenment of Indian traditional medicine intellectual property rights protection to China. Chin J Tradit Chin Med Pharm. 2016;31(11):4395–8.

    Google Scholar 

Download references

Acknowledgements

This work is supported by China Pharmaceutical University “Jointly Build World-class SCI-TECH Journals” Project Cooperation Agreements (HBJH202301) and Research on International Communication of Traditional Chinese Medicine Culture from the Perspective of “the Belt and Road”.

Funding

China Pharmaceutical University “Jointly Build World-class SCI-TECH Journals” Project Cooperation Agreements (HBJH202301). Research on International Communication of Traditional Chinese Medicine Culture from the Perspective of “the Belt and Road”.

Author information

Authors and Affiliations

Authors

Contributions

JC searched the literature, writing and editing the manuscript. ZD supervision, review and editing the manuscript. Both authors read and approved the final manuscript.

Corresponding author

Correspondence to Zuoqi Ding.

Ethics declarations

Ethics approval and consent to participate

Not applicable.

Consent for publication

All authors consent to the publication of this work in Chinese Medicine.

Competing interests

The authors declare no competing interests.

Additional information

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Chen, J., Ding, Z. Natural products as potential drug treatments for acute promyelocytic leukemia. Chin Med 19, 57 (2024). https://doi.org/10.1186/s13020-024-00928-8

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/s13020-024-00928-8

Keywords