- Open Access
Combination of shikonin with paclitaxel overcomes multidrug resistance in human ovarian carcinoma cells in a P-gp-independent manner through enhanced ROS generation
- Zhu Wang†1,
- Jianhua Yin†2,
- Mingxing Li2Email author,
- Jing Shen2,
- Zhangang Xiao2,
- Yueshui Zhao2,
- Chengliang Huang3,
- Hanyu Zhang2,
- Zhuo Zhang2,
- Chi Hin Cho2 and
- Xu Wu2Email author
© The Author(s) 2019
- Received: 8 December 2018
- Accepted: 6 March 2019
- Published: 12 March 2019
Shikonin (SKN), a naphthoquinone compound, is isolated from Chinese herbal medicine Lithospermum root and has been studied as an anticancer drug candidate in human tumor models. This study is designed to investigate whether SKN can sensitize the therapeutic effect of paclitaxel (PTX) in drug-resistant human ovarian carcinoma cells.
Human ovarian carcinoma A2780 cell along with the paired PTX-resistant A2780/PTX cells were used. The effects of SKN, PTX or their combination on cell viability were conducted using Sulforhodamine B assay. P-glycoprotein (P-gp) expression was analyzed by flow cytometry after staining with P-gp-FITC anti-body. P-gp activity was determined by a fluorometric MDR assay kit or a rhodamine 123-based efflux assay, respectively. Apoptosis was evaluated by flow cytometry after Annexin V-FITC/PI co-staining. The effect of SKN, PTX or their combination on reactive oxygen species (ROS) generation and expression of pyruvate kinase M2 (PKM2) were investigated using flow cytometry or western blotting, respectively. PKM2 activity was detected by a Pyruvate Kinase Assay Kit.
SKN/PTX co-treatment led to synergistically enhanced cytotoxicity and apoptosis in PTX-resistant ovarian cancer cells, indicating the circumvention of multidrug resistance (MDR) of PTX by SKN. Further study indicated that the MDR reversal effect of SKN was independent of inhibiting activity of the efflux transporter P-gp. Notably, SKN/PTX significantly increased the generation of intracellular ROS in A2780/PTX cells, and scavenging intracellular ROS blocked the sensitizing effects of SKN in PTX-induced cytotoxicity and apoptosis in A2780/PTX cells, but not in A2780 cells. Furthermore, SKN/PTX-induced downregulation of PKM2 (a key enzyme in glycolysis) and the suppression of its activity were inhibited by a ROS scavenger N-acetyl cysteine (NAC), suggesting that the synergy of the SKN/PTX combination may be not rely on PKM2 suppression.
These results reveal a P-gp-independent mechanism through ROS generation for the SKN/PTX combination to overcome MDR in ovarian cancer.
- Multidrug resistance
- Reactive oxygen species
- Pyruvate kinase M2
Ovarian cancer is one of the most prevalent and lethal gynecological malignancies worldwide . As ovarian cancer is particularly asymptomatic at early stage, its early diagnosis is poor . Chemotherapy and surgical therapy are the most common treatments. However, around 70% of ovarian cancer patients eventually develop advanced-staged disease and resistance to chemotherapeutic drugs . Thus, the development of new and more effective strategies to overcome multidrug resistance (MDR) is critical to successful chemotherapy.
Chemoresistance is associated with many intrinsic and extrinsic factors, including the characteristics and cellular targets of drugs, drug response of cancer cells, tumor microenvironment, and heterogeneity of tumor cells [4–6]. Most conventional anticancer drugs are capable of inducing apoptosis in cancer cells. Cancer cells usually are sensitive to drug-induced apoptosis at early stages, and become resistant eventually through abnormal regulation of apoptotic machinery [7, 8] or overexpression of efflux transporters such as P-glycoprotein (P-gp) to actively pump out anticancer drugs from cancer cells [9, 10]. Inhibition of drug transporters has long been studied as an MDR-reversal strategy [10, 11]. The major limitations of transporter inhibitors include transporters-mediated side effects and drug interactions, which has led to failure in most clinical trials [11, 12]. To circumvent MDR relevant to apoptotic defects is usually much more difficult than that relevant to transporters, because apoptotic machinery is regulated by hundreds of antiapoptotic and proapoptotic proteins . However, to overcome these apoptotic defects to re-sensitize anticancer agents to MDR tumors has been always a primary goal to achieve successful cancer treatment.
Previous studies have demonstrated that natural products are a rich source of MDR-reversal drug candidates [11, 14]. Shikonin (SKN) as a naphthoquinone is isolated from the Chinese herbal medicine Lithospermum root, and has been identified as a promising anticancer drug candidate [15, 16]. A clinical study of SKN showed that a SKN mixture was safe and effective in treating patients with advanced lung cancer . Based on numerous mechanistic studies in different types of cancer cells, SKN is capable of inducing apoptosis through targeting virous antiapoptotic and proapoptotic pathways and related proteins, such as p53 , epidermal growth factor receptor signaling , proteasomes , reactive oxygen species (ROS) generation  and suppression of glycolysis and pyruvate kinase M2 (PKM2) , and/or mediating necrosis . A recent study suggests that SKN can reduce tamoxifen resistance in resistant human breast cancer MCF-7R cells through induction of long non-coding RNA uc.57 . Given the emerging role of SKN in treating cancer and overcoming cancer MDR, this study is designed to see whether SKN can sensitize the anticancer effect of paclitaxel (PTX) in drug-resistant human ovarian carcinoma cells.
The Minimum Standards of Reporting Checklist contains details of the experimental design, and statistics, and resources used in this study (Additional file 1).
Chemicals, reagents and antibodies
Shikonin (purity > 98%) was brought from Chengdu Must Bio-Technology Co., Ltd (Sichuan, China). PTX (purity > 99%) was purchased from Dalian Meilun Biology Technology Co., Ltd. (Liaoning, China). Dulbecco’s Modified Eagle Medium (DMEM), fetal bovine serum (FBS), penicillin–streptomycin, 0.25% (w/v) trypsin/EDTA and phosphate-buffered saline (PBS) were obtained from Life Technologies (Grand Island, USA). N-acetyl cysteine (NAC) was from Absin Bioscience Co., Ltd (Shanghai, China).
Sulforhodamine B (SRB) were purchased from Sigma Aldrich (St. Louis, MO, USA). Annexin V-FITC Apoptosis Staining/Detection Kit (ab14085) was from Abcam (Cambridge, MA, USA). Rhodamine 123 (R123) and Pyruvate Kinase Assay Kit were from Solarbio (Beijing, China). P-gp conjugated FITC antibody was obtained from BD Biosciences (San Jose, USA). The primary antibodies against PKM2, PARP and GAPDH and second antibodies were purchased from Cell Signaling Technology (Danvers, MA, USA). All reagent water used was prepared with a Milli-Q apparatus (Millipore Corporation, Darmstadt, Germany). All other chemicals were of the highest purity commercially available.
Cell lines and cell culture
Human ovarian cancer A2780 cells were obtained from Boster Biotech (Wuhan, Hubei, China). PTX-resistant A2780 cells (A2780/PTX) were selected in stepwise increasing concentrations of PTX as previously described . Cells were cultured in DMEM with 10% (v/v) heat-inactivated FBS and antibiotics (100 U/mL penicillin, 100 μg/mL streptomycin) and maintained at 37 °C in a 5% CO2 atmosphere. Cells were passed using trypsin/EDTA, and the medium was changed every other day.
Cell viability assay
Exponentially growing cells were seeded in 96-well plates at a density of 3000 cells/well in 100 μL of medium and allowed to attach overnight. Cells were treated with designated drugs or their combinations for 24 h. Cell viability was determined based on SRB method as previously described .
Apoptosis was analyzed with an Annexin V-FITC/PI detection kit based on manufacturer’s protocol. Briefly, cells were collected, washed twice with cold PBS and gently resuspended in 100 μL binding buffer, followed by staining with Annexin V-FITC (5 μL) and PI (10 μL) solution, incubating for 15 min and analyzing on a flow cytometer (BD FACS CantoTM). Triplicated experiments were performed.
P-gp expression was evaluated using the antibody of P-gp conjugated FITC (BD Biosciences, San Jose, USA) as described previously . Cells were seeded into 6-well plates at a density of 2 × 105/well. The cells were harvested and incubated with 100 μL of P-gp-FITC anti-body dye-loading buffer at 37 °C for 30 min protected from light. Then flow cytometry was used for determining the FITC fluorescence. Triplicated experiments were performed.
P-gp activity assay
P-gp activity was analyzed using a fluorometric MDR assay kit (Abcam, Cambridge, UK) based on manufacturer’s protocol. Briefly, cells (6.0 × 104 cells/well) were seeded into 96-well flat clear-bottom black-wall microplates and cultured for 24 h. The cells were treated with SKN (0.5, 1 and 2 μM), PTX (1 μM) or the combination of PTX/SKN (1 μM each) for 1 h. Verapamil, a known inhibitor of P-gp, was applied as a positive control. Then 100 μL MDR dye-loading solution was added into each well and incubated at 37 °C for another 1 h in dark. Intracellular fluorescence was determined using SpectraMax M5 microplate reader with excitation wavelength of 490 nm and emission wavelength of 525 nm. Triplicated experiments were performed.
P-gp substrate efflux assay
A flow cytometry-based efflux assay was performed to investigate whether SKN influences P-gp function. Briefly, cells were incubated for 1 h with a specific fluorescent P-gp substrate R123 (0.5 μg/mL) with or without SKN (1 μM). Then, the cells were washed twice with ice-cold PBS and incubated in R123-free medium at 37 °C for 1 h with SKN or without SKN. Cells were then washed twice with ice-cold PBS until flow cytometry analysis to detect R123 fluorescence. The verapamil (20 μM) was used as the positive controls in a parallel study.
Measurement of reactive oxygen species (ROS)
Intracellular ROS levels were quantified using a fluorescent probe of 5-(and-6)-chloromethyl-2′,7′-dichlorodihydrofluorescein diacetate (CM-H2DCFDA, Life Technologies). Cells were seeded into 12-well plates at a density of 6 × 104, incubated overnight, and then treated with NAC (5 mM), SKN (1 μM), PTX (1 μM), or their combinations as specified for 4 h. The cells were stained with 1 μM CM-H2DCFDA for 30 min at 37 °C and then measured by flow cytometry (BD FACS CantoTM). Triplicated experiments were performed.
After treatment, cells were lysed with RIPA lysis buffer containing 1% protease inhibitor. Cell extracts were resolved by sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE) gel and transferred to a nitrocellulose membrane. After blocking with 5% nonfat milk in Tris-buffered saline (50 mM Tris–HCl, pH 7.5, 150 mM NaCl) containing 0.1% Tween 20, the membranes were probed with the corresponding primary antibodies. Following incubation with anti-mouse or anti-rabbit IgG horseradish peroxidase conjugate, protein bands were visualized using ECL blotting detection reagents (Clarity, Bio-Rad).
PKM2 activity assay
PKM2 activity was determined according to the Pyruvate Kinase Assay Kit (Solarbio, Beijing, China). An aliquot of 10 μL whole cell lysate was used for the assay. The change in absorbance at 340 nm on a microplate reader was recorded for 2 min.
All results are expressed as mean ± SD. Statistical analysis was carried out using GraphPad Prism 5 software (GraphPad Software, San Diego, CA, USA). One-way ANOVA followed by Dunnett’s multiple comparisons test was used for statistical comparison among multiple groups, where a p-value less than 0.05 is considered statistically significant.
Combinational treatment of SKN with PTX significantly enhances cytotoxicity to PTX-resistant ovarian cancer cells
Combination of SKN and PTX induces enhanced apoptosis
Reversal of PTX resistance by SKN is not P-gp dependent
To further confirm the results, a P-gp efflux assay was performed. We firstly demonstrated (Fig. 3c, d) that the P-gp-specific substrate R123 had a fluorescence retention in A2780 cells but not in A2780/PTX cells, suggesting an active efflux of R123 in A2780/PTX cells. The results (Fig. 3d) also showed that the P-gp inhibitor verapamil significantly increased R123 accumulation in A2780/PTX cells, while SKN had no effect. It is thus confirmed that SKN does not affect P-gp activity.
The above result indicates that SKN circumvents PTX resistance in A2780/PTX cells, not through influencing P-gp activity.
ROS production is essential for SKN/PTX-induced cell apoptosis
ROS mediates SKN-induced PKM2 suppression in A2780/PTX cells
PKM2 activity is further monitored. It is demonstrated (Fig. 7b) that the combination of SKN with PTX significantly decreased PKM2 activity while NAC pretreatment could prevent this effect. Notably, SKN but not PTX alone reduced the PKM2 activity.
Overall, the result demonstrates that SKN/PTX-induced ROS is related to PKM2 downregulation by SKN. The SKN-induced PKM2 activity suppression may be a consequence of ROS induction in A2780/PTX cells.
Successful therapy of ovarian cancer is always hindered by the symptomless at early state, the high incidence of recurrence and the development of MDR [29, 30]. The development of novel therapeutic agents or strategy for ovarian cancer therapy, particularly, to improve response to current chemotherapy, remains a key goal for achieving a better clinical outcome. SKN is a naturally occurring compounds derived from the Chinese medicinal herb Lithospermum root (Zicao, in Chinese) with potent anticancer effect. SKN is reported to induce apoptosis, necrosis or necroptosis in various cancer cell lines via regulating many signaling pathways and molecular targets. In this study, we proposed to use a combinational therapy of SKN and PTX to see the therapeutic effect in human ovarian cancer. Notably, SKN as a naturally occurring compound is able to sensitize PTX to PTX-resistant ovarian cancer cells.
Shikonin is identified as a specific and potent chemosensitizer. We firstly observed that SKN at 1 and 2 µM synergistically enhanced PTX cytotoxicity and apoptosis in A2780/PTX cells, with only additive or antagonistic effect seen on PTX-sensitive A2780 cells. This suggests that the sensitization effect of SKN is specific. Importantly, SKN is also generally a more potent chemosensitizer to overcome MDR compared to other naturally occurring compounds such as curcumin , (−)-epigallocatechin-3-gallate (EGCG) , polyoxypregnanes , where a dosage of 5–100 µM is usually required. However, whether SKN can overcome MDR in vivo needs further experiment.
MDR-reversal effect of SKN is further revealed to be P-gp-independent. P-gp as an efflux transporter is one of main causes of MDR in cancers. Due to its wide distribution in human such as liver, kidney, intestine and tissue-blood-barriers, P-gp is highly involved in drug interactions . Adverse events frequently occur when a P-gp inhibitor is used together with a conventional drug that is also a P-gp substrate and has a narrow therapeutic window . Actually, many conventionally used drugs such as paclitaxel, doxorubicin, vinblastine, and camptothecin are P-gp substrates. The fact that SKN does not affect P-gp activity may suggest a generally safe profile for using SKN in combinational chemotherapy.
Cancer cells usually have a high basal level of oxidative stress and are likely to be more vulnerable to further drug-induced ROS. Triggering ROS is thus considered as a good strategy for selectively killing cancer cells without significant cytotoxicity to normal cells . In current study, we demonstrate that SKN overcoming MDR of PTX is critically associated with enhanced cellular ROS production. As pretreatment of NAC effectively attenuated SKN/PTX-induced apoptosis in A2780/PTX cells, but not in A2780 cells, it is suggested that increased ROS generation is essential for the enhanced effect of SKN/PTX in A2780/PTX cells, and also other factors might be involved in their cytotoxic effect in A2780 cells.
Besides many molecular targets, SKN is previously known to increase ROS in cancer cells . Of particular note, it is found that PKM2 inhibition is associated with ROS accumulation induced by SKN treatment. In a previous study, SKN and its analogues were identified as PKM2 inhibitors . PKM2 is critically necessary for aerobic glycolysis in cancer cells, and is a hallmark of cancer metabolism and the main energy source for cancer cell growth and survival . Previous study suggested that PKM2 may play a role in SKN-induced cell death in human non-small cell lung cancer and breast cancer cells . In present study, SKN-mediated PKM2 suppression is found to relate with ROS generation, as pretreatment of NAC reverses this effect. It is suggested that PKM2 is not crucial for the synergistic effect of the SKN/PTX combination in in A2780/PTX cells, but is likely a downstream effector of ROS. Actually, controversies on whether PKM2 should be activated or inhibited for cancer therapy have been reported [37, 38]. Nevertheless, the cross talk between SKN-induced ROS and PKM2 regulation needs further investigations.
In present study, we demonstrate that SKN overcomes MDR of PTX in human ovarian cancer A2780/PTX cells through significantly restoring PTX-induced cytotoxicity and apoptosis. The results also show that the sensitizing effect is not P-gp-dependent and is critically associated with increased intracellular level of ROS by SKN. Moreover, the synergy of the SKN/PTX combination may be not rely on suppressing PKM2. The study suggests that SKN/PTX combination would be potentially used as an effective therapeutic regimen for ovarian cancer.
ZW, JY and ML performed the experiments. ML, XW and CHC conceived and designed the experiments. XW, YZ, JS, ZZ, CH, HZ and ZX analyzed the data and wrote the paper. All authors read and approved the final manuscript.
The authors declare that they have no competing interests.
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The work was funded by the National Natural Science Foundation of China (NO. 81703807, NO. 81803237) and the Joint Funds of the Southwest Medical University & Luzhou, Sichuan Province, China (NO. 2018LZXNYD-ZK34, NO. 2017LZXNYD-J02).
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