Cryptotanshinone attenuates the stemness of non-small cell lung cancer cells via promoting TAZ translocation from nuclear to cytoplasm
Chinese Medicine volume 15, Article number: 66 (2020)
Cancer stem cells (CSCs) are regarded as the root of tumor progression, thus representing an anti-cancer therapy through targeting this cell sub-population.
Non-small cell lung cancer (NSCLC) CSCs were enriched by non-adherent spheroid formation analysis. Lentivirus infection was used to stably change gene expression. Cell cycle, EdU incorporation, cell apoptosis, cell viability, ALDH1 activity, spheroid formation and in vivo tumor initiation assays were performed to detect the effects of Cryptotanshinone (CT), a traditional Chinese herb medicine, on the stemness of NSCLC cells. RNA-sequencing combined qRT-PCR and western blot analysis were constructed to explore the underlying mechanism contributing to CT-mediated effects.
CT could attenuate the stemness of NSCLC CSCs, as evident by the reduced spheroid formation ability, stemness marker expression and ALDH1 activity. Additionally, CT provoked NSCLC CSCs entry into the cell cycle. RNA-sequencing analysis showed that Hippo signaling pathway was highly enriched in NSCLC CSCs with CT treatment. Further experiments disclosed that CT decreased TAZ (a regulatory master of Hippo pathway) expression via promoting its nuclear-cytoplasm translocation in NSCLC CSCs. Also, overexpression of TAZ partially saved the attenuation of CT on the stemness of NSCLC CSCs. Notably, CT enhanced the sensitivity of tyrosine kinase inhibitor (TKI) and chemotherapy in NSCLC CSCs.
This work reveals that CT attenuates NSCLC CSC stemness, implying the possibility of CT as an adjuvant therapy for NSCLC.
Lung cancer is common malignant tumor in clinic with a high morbidity and mortality and ranks the first in tumors, among which non-small cell lung cancer (NSCLC) accounts for 80% . Because NSCLC has no obvious symptoms in the early stage, most of the patients are diagnosed with advanced stage. At present, radiotherapy, chemotherapy and targeted drug therapy are the main treatment in clinic, however, many patients, such as KRAS-mutant NSCLC, are not response or resistant to chemotherapy and targeted drug therapy . Therefore, it is important to find novel ways to treat NSCLC.
Tumor initiating cells, also known as cancer stem cells (CSCs), have been regarded as the root of tumorigenesis . It was found that targeting CSCs or attenuating the stemness could suppress tumor development, progression and decrease drug resistance. For example, salinomycin kills breast CSCs by sequestering iron in lysosomes and thus arrest tumor progression [4, 5]. Aspirin attenuates the chemoresistance of breast cancer cells by suppressing signaling necessary for CSC progression . Resveratrol exerts its anti-tumor effects in breast cancer via inducing the apoptosis of CSCs through modulating fatty acid synthase expression . Cryptotanshinone (CT) is the main lipid-soluble component and one of the many monomers of Salvia miltiorrhiza . CT has been shown to harbor many pharmacological activities, such as anti-cholinesterase, anti-inflammatory, anti-oxidation, anti-bacterial, anti-tumor and anti-platelet aggregation . Recent study has shown that as the main components of Salvia miltiorrhiza, CT, tanshinone I dihydrotanshinone and tanshinone IIA are the ideal inhibitors of P-gp , which is overexpressed in CSCs . CT and tanshinone IIA are both the lipid-soluble constituents of Salvia miltiorrhiza, notably, tanshinone IIA has been shown to reduce the stemness of cervix carcinoma cells , glioma stem cells  and breast cancer stem cells . A previous study has shown that CT could reduce the spheroid formation capacity and downregulate the expression of stemness regulators in prostate cells and prostate CSCs . Additionally, CT enhances paclitaxel sensitivity of tongue squamous cell carcinoma through suppressing the JAK/STAT3 pathway . These results imply that CT may hold the similar effects in regulating the stemness of tumor cells as tanshinone IIA.
In the current work, NSCLC CSCs were enriched and collected by spheroid formation analysis, and subjected to experiments. We found that CT reduced the stemness of NSCLC CSCs in a concentration-dependent manner. Additionally, CT provoked the NSCLC CSCs into cell cycle. The mechanistic studies showed that CT activated the Hippo pathway, as evident by increasing the nuclear-cytoplasm translocation of TAZ. Finally, it was found that CT sensitized NSCLC CSCs to chemotherapy and tyrosine kinase inhibitor (TKI) treatment. These results suggest that CT could be used as a combination with TKI or chemotherapy for NSCLC patients.
Materials and methods
Cell cultures and reagents
Human NSCLC cell lines A549 and H1299 were purchased from Cobioer (Shanghai, China). Cells were maintained in 1640 medium (Hyclone, South Logan, UT) containing 1% streptomycin and penicillin as well as 10% fetal bovine serum (Hyclone), and cells were cultured at 37 °C under humidified air with 5% CO2. Cell lines have been tested and authenticated by short tandem repeat (STR) DNA profiling method. Cisplatin and Erlotinib were purchased from Selleck Chemicals (Houston, TX, USA).
Quantitative real-time PCR (qRT-PCR)
Total RNA was extracted using TRIzol™ Reagent (Thermo Fisher Scientific, Waltham, MA, USA) and cDNA was reversely synthesized with High-Capacity cDNA Reverse Transcription Kit with RNase Inhibitor (Thermo Fisher Scientific). mRNA expression levels were measured using Rapid SYBR® Green qPCR kit (Sigma, St.Louis, MO) on on the Illumina Eco™ Real-Time PCR System. GAPDH expression was used as an endogenous reference. 2−△△ct method was performed to measure the relative expression levels.
RNA sequencing analysis
RNA-sequencing analysis was constructed by Genedenovo (Guangzhou, China).
Western blot analysis
Lentivirus vector construction
TAZ overexpression lentivirus, knockdown lentivirus and control vectors were constructed by Biomics (Nantong, China), denoted as Len-TAZ and Len-TAZ-kd.
Cell cycle assay
Cell cycle analysis was performed with the cell cycle assay kit (Yifeixue, Nanjing, China) following the recommendation procedures on flow cytometry.
5-Ethynyl-2′-deoxyuridine (EdU) incorporation assay
EdU incorporation assay was performed to measure the speed of DNA synthesis with a BeyoClick™ EdU-647 kit (Beyotime, Beijing, China).
Cell apoptosis assay
Annexin V-FITC/PI Apoptosis Detection Kit (Meilune, China) was used to detect cell apoptosis.
Cell viability assay
Cells were digested and seeded into 96-well plates at 4000 cells/well, after 12 h, cells were treated drug for 48 h. Then cell viability was measured using Cell Counting Kit-8 (Meilunbio, Dalian, China).
Spheroid formation analysis
The process is referred to the previous study . Briefly, NSCLC cells were maintained in DMEM-F12 medium containing B27 (Sigma, 20 ng/ml) and EGF (BD Biosciences, San Jose, CA, 10 ng/ml) in non-adherent 24-well plates (Corning, NY) at 1000 cells/well for 10 days. After then, spheroids with more than 50 μm were photographed and counted. For analysis on spheroids, spheroids were collected, trypsinized and re-seeded in plates. The spheroid-derived cells were incubated until the end of each experiment, and fresh spheroids were collected for each experiments.
ALDH1 activity assay
Acetaldehyde dehydrogenase (ALDH) Assay Kit (Solarbio, Beijing, China) was used to determine ALDH1 activity in NSCLC cells according to the manufacturer’s protocols.
In vivo tumor initiation assays
All animal experiments were performed with the approval of Ethics Committee for Animal Experimentation of Bengbu Medical College. 6–8 weeks of athymic BALB/c nude mice were purchased from the Gempharmatech (Nanjing, China). For analyzing of CT on the tumorigenic ability of NSCLC spheroids, spheroids were co-cultured with CT for 72 h before implanting in mice, and then subcutaneously implanted in mice with the same cell number. After 12 days, all mice were killed and tumor tissues were collected and weighed. The tumor-initiating ability was evaluated by calculating the tumor-formation rate. The CSC rate was calculated using ELDA software (http://bioinf.wehi.edu.au/software/elda/).
Results were expressed as Mean ± SD and analyzed using Graphpad Prism (Version X; La Jolla, CA, USA). Student’s t test was used to assess the differences between groups. P < 0.05 was considered statistically significant.
Non-adherent spheroids formed by NSCLC cells exhibit the CSCs-like traits
Because non-adherent spheres have been shown to exhibit CSCs-like traits , NSCLC CSCs were enriched and collected via spheroid formation analysis. The CSCs-like traits were firstly identified through examining stemness marker expression, spheroid-forming ability and ALDH1 activity. As expected, the non-adherent spheroids harbored higher expression levels of stemness markers (oct4 and nanog), stronger capacity of spheroid formation and higher level of ALDH1 activity compared to adherent NSCLC cells (Fig. 1a–e). Since CSCs are always at a quiescent stage which helps them escape from being killed by drugs , we compared the cell cycle status between NSCLC cells and NSCLC non-adherent spheroids. It was found that NSCLC non-adherent spheroids exhibited a decreased EdU incorporation (Fig. 1f, g) and expression of differentiation genes (CD64 and CD11c)  (Fig. 1h, i). Additionally, NSCLC non-adherent spheroids held the remarkably upregulated ratio of quiescent (G0) cells and downregulated S/G2/M cells (Fig. 1j). Notably, cell apoptosis displayed no difference between NSCLC cells and non-adherent spheroids (Fig. 1k). Overall, these results indicate that the non-adherent NSCLC spheroids could be used as the model of NSCLC CSCs.
CT attenuates the stemness of NSCLC CSCs
Following this, we investigated the CT effects on the stemness of NSCLC CSCs. As shown in Fig. 2a–d, CT displayed a stronger inhibitory effect on the viability of NSCLC CSCs than that in NSCLC cells, characterized as the lower IC50 values. Additionally, CT reduced the expression of stemness markers (oct4 and nanog) in a concentration-dependent manner (Fig. 2e–g). The spheroid-forming ability of NSCLC CSCs was attenuated by CT treatment, which is supported by the decreased spheroid number and size (Fig. 2h, i). CT decreased the activity of ALDH1 in NSCLC CSCs (Fig. 2j). Furthermore, the tumor-initiation ability of NSCLC CSCs was significantly attenuated by CT treatment, which is characterized by the decrease of tumor-formation rate and CSC rate (Fig. 2k, l).
CT assists the NSCLC CSCs enter cell cycle
To further confirm the CT effects on the stemness of NSCLC CSCs, the differentiation, proliferative and clonogenic capacity was evaluated. As shown in Fig. 3a, b, NSCLC CSCs treated with CT displayed an increased EdU incorporation compared with control group, whereas the apoptosis of NSCLC CSCs was unaffected. Furthermore, the reduced ratios of quiescent (G0) cells and an increased S/G2/M cells were observed in NSCLC CSCs with CT treatment (Fig. 3c). Additionally, the expression of differentiation genes (CD64 and CD11c) was increased by CT in NSCLC CSCs (Fig. 3d, e). Since CDK3 is essential for G0 phase exit in cell cycle, CDK3 expression was determined and results indicated that CT increased the expression CDK3 in NSCLC CSCs (Fig. 3f). As a result, these results demonstrate that CT suppresses the stemness of NSCLC CSCs.
Hippo pathway is activated in NSCLC CSCs with CT treatment
Then we explored the mechanisms by which CT attenuates the stemness of NSCLC CSCs. RNA-sequencing was performed in NSCLC CSCs with or without CT treatment. As shown in Fig. 4a, b, one of the mostly enriched pathways is Hippo pathway, which plays important roles in CSC expansion. However, the expression of the upstream regulators of Hippo pathway, the large tumor suppressor 1/2 (LATS1/2) was unchanged, but the downstream executor TAZ and its target genes (CTGF, TIF-1 and Smad2) expression was significantly decreased (Fig. 4b). Additionally, gene set enrichment analysis (GSEA) of this dataset revealed a positive enrichment of stem cell-differentiated signatures in NSCLC CSCs with CT treatment, and the embryonic stem cell function and adult tissue stem modules exhibited a negative enrichment (Fig. 4c–e), this effect further confirmed the inhibitory roles of CT on the stemness of NSCLC CSCs. As the expression of TAZ is regulated by its nuclear-cytoplasm translocation, we evaluated the effect of CT on the translocation from nuclear to cytoplasm of TAZ. To our surprise, it was found that the expression of TAZ in nuclear was decreased, while its expression in cytoplasm was increased (Fig. 5a, b). IF experiments obtained the consistent results (Fig. 5c). This effect means that CT promotes TAZ translocation from nuclear to cytoplasm.
CT reduces the stemness of NSCLC CSCs dependent on TAZ expression
Then, we investigated whether CT-mediated effects were dependent on TAZ expression. TAZ was overexpressed in NSCLC CSCs with CT treatment via lentivirus infection. The infection efficiency was examined (Fig. 6a, b). Additionally, overexpression of TAZ partially reversed the inhibitory effects of CT on the stemness of NSCLC CSCs, which was supported by the rescue of stemness marker expression (Fig. 6c–e), spheroid-forming ability (Fig. 6f, g) and ALDH1 activity (Fig. 6h).
CT sensitizes NSCLC CSCs to TKI treatment and chemotherapy
Since CSCs are usually resistant to common drug treatment, we finally evaluated whether CT is involved in drug sensitivity of NSCLC CSCs. Because TKIs and chemotherapy are two mostly used for NSCLC treatment, Erlotinib and Cisplatin were chosen as the research subjects. As expected, NSCLC CSCs indeed exhibited an extent of resistance to Erlotinib and Cisplatin through detecting cell viability, however, CT re-sensitized NSCLC CSCs to Erlotinib and Cisplatin treatment, this effect was attenuated by TAZ overexpression (Fig. 7a–d). Therefore, our results confirm that TAZ is essential for CT-mediated inhibition on the stemness of NSCLC CSCs.
Our work discloses the inhibitory roles of CT in the stemness of NSCLC cells, including regulating the self-renewal capability and drug sensitivity, provoking the NSCLC CSCs entry into cell cycle. Although the previous studies have shown that CT has been proved to be an ideal inhibitor of P-gp  and inhibit the spheroid formation capacity and downregulate the expression of stemness genes in prostate cells and prostate CSCs , this study firstly reveals the CT roles in NSCLC CSC progression.
The Hippo pathway is an evolutionarily conserved signaling which play critical roles in cell differentiation and regulating organ size . Alterations in Hippo pathway have been shown in regulating the stemness and targeting this pathway is correlated with CSCs progression. For example, as the stemness regulator master, sox2 maintains cancer cell stemness by antagonizing the Hippo pathway . The tumor suppressor, STADR13-correlated competing endogenous RNA (ceRNA) network attenuates breast cancer cell stemness via a direct inhibition on YAP/TAZ activity (the key executors of Hippo pathway) through activating Hippo pathway . MORC2 promotes the stemness and tumorigenesis by facilitating DNA methylation-dependent silencing of Hippo signaling in hepatocellular carcinoma cells . Notably, as the critical executors of Hippo pathway, the WW Domain-Containing Proteins YAP and TAZ have been shown to maintain the stemness and tissue homeostasis, and facilitate tumorigenesis . However, in the current study, TAZ expression but not YAP expression was reduced in NSCLC cells with CT treatment. We speculated that this different effect may be due to the different structure of YAP and TAZ, which should be explored in the future.
KRAS mutations are frequent in non-small cell lung cancer (NSCLC). However, it is difficult to targeting KRAS or the downstream/upstream effectors, such as tyrosine kinase inhibitors (TKIs). Here, NSCLC cells with KRAS mutation or not (A549 with KRAS mutation and H1299 with wild-type KRAS) were chosen as the research subjects. Our results demonstrate that CT attenuated the stemness of the KRAS-mutant and –wild-type NSCLC cells, implying CT has no selectivity on NSCLC cells. Notably, although PI3K/Akt pathway has been shown to promote tumor progression [26, 27] and Akt and PI3K inhibitors are in clinical trials , most of them failed in NSCLC and resistance always happens. The previous work indicates that PI3K/Akt signaling is suppressed in quiescent acute myeloid leukemia stem cells  and inhibition of AKT activity increased the ratio of the G0-phased cells . And limonin attenuates the stemness of hepatocellular carcinoma cells by reducing cellular quiescence through activating PI3K/Akt signaling . These results suggest that PI3K/Akt activity was different in cells with or without stemness. As shown in Fig. 4 results, PI3K/Akt pathway was activated in NSCLC CSCs with CT treatment, and overexpression of TAZ just partially reversed the inhibitory effects of CT (Fig. 5), demonstrating that CT may attenuate the stemness of NSCLC CSCs through other pathways, such as PI3K/Akt. In addition, in vivo experiments should be constructed to confirm the conclusion. Importantly, Salvia miltiorrhiza has the highest application frequency in the compatibility of traditional Chinese medicine for promoting blood circulation and removing blood stasis and the other main components of Salvia miltiorrhiza, such as tanshinone I, dihydrotanshinone and tanshinone IIA, have been confirmed to be involved in CSC progression [10,11,12,13,14,15]. Combined with these previous results, this study attempts to use modern medical mechanism to study and explain the theory of traditional Chinese medicine, reveal the potential mechanism of blood-activiating and stasis-dissolving drugs to resist chemoresistance of breast cancer. We strongly believe that Salvia miltiorrhiza, which is a typical blood-activiating and stasis-dissolving drug and has been proved to be used in clinic, may be used to target CSCs, this could be explored in the future.
All in all, our results indicate that CT reduces NSCLC CSC stemness, providing a potential drug for combinatory using for NSCLC treatment.
Availability of data and materials
All data generated or analysed during this study are included in this published article.
Cancer stem cells
Non-small cell lung cancer
Quantitative real-time PCR
Tyrosine kinase inhibitor
Short tandem repeat
Large tumor suppressor 1/2
Gene set enrichment analysis
Competing endogenous RNA
Lemjabbar-Alaoui H, Hassan OU, Yang YW, Buchanan P. Lung cancer: biology and treatment options. Biochem Biophys Acta. 2015;1856:189–210.
Mainardi S, Mulero-Sanchez A, Prahallad A, Germano G, Bosma A, Krimpenfort P, Lieftink C, Steinberg JD, de Wit N, Goncalves-Ribeiro S, Nadal E, Bardelli A, Villanueva A, Bernards R. SHP2 is required for growth of KRAS-mutant non-small-cell lung cancer in vivo. Nat Med. 2018;24:961–7.
Li K, Zhang TT, Hua F, Hu ZW. Metformin reduces TRIB3 expression and restores autophagy flux: an alternative antitumor action. Autophagy. 2018;14:1278–9.
Sun J, Luo Q, Liu L, Yang X, Zhu S, Song G. Salinomycin attenuates liver cancer stem cell motility by enhancing cell stiffness and increasing F-actin formation via the FAK-ERK1/2 signalling pathway. Toxicology. 2017;384:1–10.
Mai TT, Hamai A, Hienzsch A, Caneque T, Muller S, Wicinski J, Cabaud O, Leroy C, David A, Acevedo V, Ryo A, Ginestier C, Birnbaum D, Charafe-Jauffret E, Codogno P, Mehrpour M, Rodriguez R. Salinomycin kills cancer stem cells by sequestering iron in lysosomes. Nature chemistry. 2017;9:1025–33.
Saha S, Mukherjee S, Khan P, Kajal K, Mazumdar M, Manna A, Mukherjee S, De S, Jana D, Sarkar DK, Das T. Aspirin suppresses the acquisition of chemoresistance in breast cancer by disrupting an NFkappaB-IL6 signaling axis responsible for the generation of cancer stem cells. Cancer Res. 2016;76(7):2000–12.
Pandey PR, Okuda H, Watabe M, Pai SK, Liu W, Kobayashi A, Xing F, Fukuda K, Hirota S, Sugai T, Wakabayashi G, Koeda K, Kashiwaba M, Suzuki K, Chiba T, Endo M, Fujioka T, Tanji S, Mo YY, Cao D, Wilber AC, Watabe K. Resveratrol suppresses growth of cancer stem-like cells by inhibiting fatty acid synthase. Breast Cancer Res Treat. 2011;130:387–98.
Zhang W, Yu W, Cai G, Zhu J, Zhang C, Li S, Guo J, Yin G, Chen C, Kong L. A new synthetic derivative of cryptotanshinone KYZ3 as STAT3 inhibitor for triple-negative breast cancer therapy. Cell Death Dis. 2018;9:1098.
Chen W, Lu Y, Chen G, Huang S. Molecular evidence of cryptotanshinone for treatment and prevention of human cancer. Anticancer Agents Med Chem. 2013;13:979–87.
Lee WY, Cheung CC, Liu KW, Fung KP, Wong J, Lai PB, Yeung JH. Cytotoxic effects of tanshinones from Salvia miltiorrhiza on doxorubicin-resistant human liver cancer cells. J Nat Prod. 2010;73:854–9.
Bauml JM, Mick R, Ciunci C, Aggarwal C, Davis C, Evans T, Deshpande C, Miller L, Patel P, Alley E, Knepley C, Mutale F, Cohen RB, Langer CJ. Pembrolizumab after completion of locally ablative therapy for oligometastatic non-small cell lung cancer: a phase 2 trial. JAMA Oncol. 2019;5(9):1283–90.
Qin J, Shi H, Xu Y, Zhao F, Wang Q. Tanshinone IIA inhibits cervix carcinoma stem cells migration and invasion via inhibiting YAP transcriptional activity. Biomed Pharmacother. 2018;105:758–65.
Yang L, Guo H, Dong L, Wang L, Liu C, Wang X. Tanshinone IIA inhibits the growth, attenuates the stemness and induces the apoptosis of human glioma stem cells. Oncol Rep. 2014;32:1303–11.
Lin C, Wang L, Wang H, Yang L, Guo H, Wang X. Tanshinone IIA inhibits breast cancer stem cells growth in vitro and in vivo through attenuation of IL-6/STAT3/NF-kB signaling pathways. J Cell Biochem. 2013;114:2061–70.
Zhang Y, Cabarcas SM, Zheng JI, Sun L, Mathews LA, Zhang X, Lin H, Farrar WL. Cryptotanshinone targets tumor-initiating cells through down-regulation of stemness genes expression. Oncol Lett. 2016;11:3803–12.
Wang Y, Lu HL, Liu YD, Yang LY, Jiang QK, Zhu XJ, Fan HN, Qian Y. Cryptotanshinone sensitizes antitumor effect of paclitaxel on tongue squamous cell carcinoma growth by inhibiting the JAK/STAT3 signaling pathway. Biomed Pharmacother. 2017;95:1388–96.
Tang Z, Tang Y, Li L, Liu T, Yang J. Limonin provokes hepatocellular carcinoma cells with stemness entry into cycle via activating PI3K/Akt signaling. Biomed Pharmacother. 2019;117:109051.
Li Z, Liu H, Zhong Q, Wu J, Tang Z. LncRNA UCA1 is necessary for TGF-beta-induced epithelial–mesenchymal transition and stemness via acting as a ceRNA for Slug in glioma cells. FEBS Open Bio. 2018;8:1855–65.
Zheng L, Xiang C, Li X, Guo Q, Gao L, Ni H, Xia Y, Xi T. STARD13-correlated ceRNA network-directed inhibition on YAP/TAZ activity suppresses stemness of breast cancer via co-regulating Hippo and Rho-GTPase/F-actin signaling. J Hematol Oncol. 2018;11:72.
Kreso A, O’Brien CA, van Galen P, Gan OI, Notta F, Brown AM, Ng K, Ma J, Wienholds E, Dunant C, Pollett A, Gallinger S, McPherson J, Mullighan CG, Shibata D, Dick JE. Variable clonal repopulation dynamics influence chemotherapy response in colorectal cancer. Science. 2013;339:543–8.
Hu J, Zheng L, Shen X, Zhang Y, Li C, Xi T. MicroRNA-125b inhibits AML cells differentiation by directly targeting Fes. Gene. 2017;620:1–9.
Britschgi A, Duss S, Kim S, Couto JP, Brinkhaus H, Koren S, De Silva D, Mertz KD, Kaup D, Varga Z, Voshol H, Vissieres A, Leroy C, Roloff T, Stadler MB, Scheel CH, Miraglia LJ, Orth AP, Bonamy GM, Reddy VA, Bentires-Alj M. The Hippo kinases LATS1 and 2 control human breast cell fate via crosstalk with ERalpha. Nature. 2017;541(7638):541–5.
Basu-Roy U, Bayin NS, Rattanakorn K, Han E, Placantonakis DG, Mansukhani A, Basilico C. Sox2 antagonizes the Hippo pathway to maintain stemness in cancer cells. Nat Commun. 2015;6:6411.
Wang T, Qin ZY, Wen LZ, Guo Y, Liu Q, Lei ZJ, Pan W, Liu KJ, Wang XW, Lai SJ, Sun WJ, Wei YL, Liu L, Guo L, Chen YQ, Wang J, Xiao HL, Bian XW, Chen DF, Wang B. Epigenetic restriction of Hippo signaling by MORC2 underlies stemness of hepatocellular carcinoma cells. Cell Death Differ. 2018;25:2086–100.
Chen YA, Lu CY, Cheng TY, Pan SH, Chen HF, Chang NS. WW Domain-Containing Proteins YAP and TAZ in the Hippo Pathway as Key Regulators in Stemness Maintenance, Tissue Homeostasis, and Tumorigenesis. Front Oncol. 2019;9:60.
Wang S, Zhu M, Wang Q, Hou Y, Li L, Weng H, Zhao Y, Chen D, Ding H, Guo J, Li M. Alpha-fetoprotein inhibits autophagy to promote malignant behaviour in hepatocellular carcinoma cells by activating PI3K/AKT/mTOR signalling. Cell Death Dis. 2018;9:1027.
Ma XL, Shen MN, Hu B, Wang BL, Yang WJ, Lv LH, Wang H, Zhou Y, Jin AL, Sun YF, Zhang CY, Qiu SJ, Pan BS, Zhou J, Fan J, Yang XR, Guo W. CD73 promotes hepatocellular carcinoma progression and metastasis via activating PI3K/AKT signaling by inducing Rap1-mediated membrane localization of P110beta and predicts poor prognosis. J Hematol Oncol. 2019;12:37.
Fransecky L, Mochmann LH, Baldus CD. Outlook on PI3K/AKT/mTOR inhibition in acute leukemia. Mol Cell Ther. 2015;3:2.
Lechman ER, Gentner B, Ng SWK, Schoof EM, van Galen P, Kennedy JA, Nucera S, Ciceri F, Kaufmann KB, Takayama N, Dobson SM, Trotman-Grant A, Krivdova G, Elzinga J, Mitchell A, Nilsson B, Hermans KG, Eppert K, Marke R, Isserlin R, Voisin V, Bader GD, Zandstra PW, Golub TR, Ebert BL, Lu J, Minden M, Wang JCY, Naldini L, Dick JE. miR-126 regulates distinct self-renewal outcomes in normal and malignant hematopoietic stem cells. Cancer Cell. 2016;29:602–6.
Dey-Guha I, Wolfer A, Yeh AC, Darp R, Leon E, Wulfkuhle J, Petricoin EF, Wittner BS, Ramaswamy S. Asymmetric cancer cell division regulated by AKT. Proc Natl Acad Sci USA. 2011;108:12845–50.
This work was supported in part by National Natural Science Foundation of China under Grant 81800090.
This work is supported by the Natural Science Foundation of China under Grant 81800090. Linling Jin, Zhenzhen Wu, Yanli Wang, Xin Zhao
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Jin, L., Wu, Z., Wang, Y. et al. Cryptotanshinone attenuates the stemness of non-small cell lung cancer cells via promoting TAZ translocation from nuclear to cytoplasm. Chin Med 15, 66 (2020). https://doi.org/10.1186/s13020-020-00348-4
- Non-small cell lung cancer