Hsps odpowiedzialne za oporność komórek raka szyjki macicy na indukcję apoptozy pod wpływem ostolu i tamoksyfenu
Joanna Jakubowicz-Gil 1 , Roman Paduch 2 , Krystyna Skalicka-Woźniak 3 , Joanna Sumorek-Wiadro 1 , Adrian Zając 1 , Antoni Gawron 1Abstrakt
Aim: The aim of the present study was to investigate the efficacy of osthole (7-metoxy-8-isopenthenocoumarin) alone and combined with tamoxifen (TAM) in the elimination of human cervical cancer cells via programmed death. The involvement of heat shock proteins, i.e. well-known molecular chaperones, will be investigated. Material/Methods: Three human cervical cancer cell lines, infected with human papilloma virus (HPV), i.e. HeLa (HPV 18), SiHa (HPV 16), and CaSki (HPV 16 and 18), were used in the experiments. After osthole and TAM treatment, cells stained with fluorochromes were analyzed microscopically according to apoptotic, autophagic, and necrotic morphology. Hsp27, Hsp72, and Hsp90 levels were analyzed by immunoblotting. Transfection with specific siRNA was used for blocking of Hsp expression. Results: In the HeLa, CaSki, and SiHa cell lines, osthole and TAM applied alone had no significant effect on cell death induction. This was correlated with an overexpression of heat shock proteins 27, 72, and 90. In the case of a combination of both drugs, the level of apoptosis was elevated only in SiHa cells. Preincubation with osthole followed by TAM addition as well as simultaneous incubation with both drugs was the most effective. This was correlated with the inhibition of Hsp27, Hsp72, and Hsp90 expression. Blocking of Hsp expression with specific siRNA increased the sensitivity of the studied cell lines to the induction of apoptosis, but not to autophagy or necrosis. Conclusions: Our results indicated that the elimination of heat shock proteins from cervical cancer cells sensitized them to initiation of apoptosis after osthole and tamoxifen treatment.
Przypisy
- 1. Ajiro M., Zheng Z.M.: E6^E7, a novel splice isoform protein of human papillomavirus 16, stabilizes viral E6 and E7 oncoproteins via HSP90 and GRP78. MBio, 2015; 6: e02068–e020614
Google Scholar - 2. Ariazi E.A., Cunliffe H.E., Lewis-Wambi J.S., Slifker M.J., Willis A.L., Ramos P., Tapia C., Kim H.R., Yerrum S., Sharma C.G., Nicolas E., Balagurunathan Y., Ross E.A., Jordan V.C.: Estrogen induces apoptosis in estrogen deprivation-resistant breast cancer through stress responses as identified by global gene expression across time. Proc. Natl. Acad. Sci. USA, 2011; 108: 18879–18886
Google Scholar - 3. Barot K.P., Jain S.V., Kremer L., Singh S., Gathe M.D.: Recent advances and therapeutic journey of coumarins: current status and perspectives. Med. Chem. Res., 2015; 24: 2771–2798
Google Scholar - 4. Castle P.E., Ashfaq R., Ansari F., Muller C.Y.: Immunohistochemical evaluation of heat shock proteins in normal and preinvasive lesions of the cervix. Cancer Lett., 2005; 229: 245–252
Google Scholar - 5. Ciocca D.R., Calderwood S.K.: Heat shock proteins in cancer: diagnostic, prognostic, predictive, and treatment implications. Cell Stress Chaperones, 2005; 10: 86–103
Google Scholar - 6. Den Boom J.A., Pyeon D., Wang S.S., Horswill M., Schiffman M., Sherman M., Zuna R.E., Wang Z., Hewitt S.M., Pearson R., Schott M., Chung L., He Q., Lambert P.O, Walker J., et al.: Molecular transitions from papillomavirus infection to cervical precancer and cancer: Role of stromal estrogen receptor signalling. Proc. Natl. Acad. Sci. USA, 2015; 112: E3255–E3264
Google Scholar - 7. Grenman S., Shapira A., Carey T.E.: In vitro response of cervical cancer cell lines CaSki, HeLa and ME-180 to the antiestrogen tamoxifen. Gynecol. Oncol., 1988; 30: 228–238
Google Scholar - 8. Jakubowicz-Gil J., Bądziul D., Langner E., Wertel I., Zając A., Rzeski W.: Temozolomide and sorafenib as programmed cell death inducers of human glioma cells. Pharmacol. Rep., 2017; 69: 779–787
Google Scholar - 9. Jarząb A., Grabarska A., Kiełbus M., Jeleniewicz W., Dmoszyńska-Graniczka M., Skalicka-Woźniak K., Sieniawska E., Polberg K., Stepulak A.: Osthole induces apoptosis, suppresses cell-cycle progression and proliferation of cancer cells. Anticancer Res., 2014; 34: 6473–6480
Google Scholar - 10. Jiang G., Liu J., Ren B., Tang Y, Owusu L., Li M., Zhang J., Liu L., Li W.: Anti-tumor effects of osthole on ovarian cancer cells in vitro. J. Ethnopharmacol., 2016; 193: 368–376
Google Scholar - 11. Khar A., Ali A.M.: Serum protects HeLa cells from antiestrogen effects in culture. Eur. J. Cancer Clin. Oncol., 1987; 23: 761–763
Google Scholar - 12. Lo W.Y., Lai C.C., Hua C.H., Tsai M.H., Huang S.Y., Tsai C.H., Tsai F.J.: S100A8 is identified as a biomarker of HPV18-infected oral squamous cell carcinomas by suppression subtraction hybridization, clinical proteomics analysis, and immunohistochemistry staining. J. Proteome Res., 2007; 6: 2143–2151
Google Scholar - 13. Majumdar S.K., Valdellon J.A., Brown K.A.: In vitro investigations on the toxicity and cell death induced by tamoxifen on two non-breast cancer cell types. J. Biomed. Biotechnol., 2001; 1: 99–107
Google Scholar - 14. Radin D.P., Patel P.: Delineating the molecular mechanisms of tamoxifen’s oncolytic actions in estrogen receptor-negative cancers. Eur. J. Pharmacol., 2016; 781: 173–180
Google Scholar - 15. Rondón-Lagos M., Villegas V.E., Rangel N., Sánchez M.C., Zaphiropoulos P.G.: Tamoxifen resistance: emerging molecular targets. Int. J. Mol. Sci., 2016; 17: E1357
Google Scholar - 16. Salami S., Karami-Tehrani F.: Biochemical studies of apoptosis induced by tamoxifen in estrogen receptor positive and negative breast cancer cell lines. Clin. Biochem., 2003; 36: 247–253
Google Scholar - 17. Xu X., Zhang Y., Qu D., Jiang T., Li S.: Osthole induces G2/M arrest and apoptosis in lung cancer A549 cells by modulating PI3K/Akt pathway. J. Exp. Clin. Cancer Res., 2011; 30: 33
Google Scholar - 18. Zhang L., Jiang G., Yao F., He Y., Liang G., Zhang Y., Hu B., Wu Y., Li Y., Liu H.: Growth inhibition and apoptosis induced by osthole, a natural coumarin, in hepatocellular carcinoma. PLoS One, 2012; 7: e37865
Google Scholar - 19. Zhou L., Zhu T., Yang L., Wang B., Liang X., Lu L., Tsao Y.P., Chen S.L., Li J., Xiao X.: Long-term protection against human papillomavirus e7-positive tumor by a single vaccination of adeno-associated virus vectors encoding a fusion protein of inactivated e7 of human papillomavirus 16/18 and heat shock protein 70. Hum. Gene Ther., 2010; 21: 109–119
Google Scholar - 20. Zong J., Wang C., Liu B., Liu M., Cao Y., Sun X., Yao Y., Sun G.: Human hsp70 and HPV16 oE7 fusion protein vaccine induces an effective antitumor efficacy. Oncol. Rep., 2013; 30: 407–412
Google Scholar