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Roles of the Bcl-2/Bax Ratio, Caspase-8 and 9 in Resistance of Breast Cancer Cells to Paclitaxel

  • Sharifi, Simin (Department of Pharmaceutical Biotechnology, Faculty of Pharmacy, Tabriz University of Medical Sciences) ;
  • Barar, Jaleh (Department of Pharmaceutical Biotechnology, Faculty of Pharmacy, Tabriz University of Medical Sciences) ;
  • Hejazi, Mohammad Saeid (Department of Pharmaceutical Biotechnology, Faculty of Pharmacy, Tabriz University of Medical Sciences) ;
  • Samadi, Nasser (Department of Pharmaceutical Biotechnology, Faculty of Pharmacy, Tabriz University of Medical Sciences)
  • Published : 2014.11.06

Abstract

The goal of this study was to establish paclitaxel resistant MCF-7 cells, as in vitro model, to identify the molecular mechanisms leading to acquired chemoresistance in breast cancer cells. Resistant cells were developed by stepwise increasing exposure to paclitaxel. Gene expression levels of Bax and Bcl-2 along with protein levels of caspase-8 and caspase-9 were evaluated in two resistant cell lines (MCF-7/Pac64 and MCF-7/Pac5 nM). Morphological modifications in paclitaxel resistance cells were examined by light microscopy and fluorescence activated cell sorting (FACS). As an important indicator of resistance to chemotheraputic agents, the Bcl-2/Bax ratio showed a significant increase in both MCF-7/Pac5nM and MCF-7/Pac 64nM cells (p<0.001), while caspase-9 levels were decreased (p<0.001) and caspase-8 was increased (p<0.001). FACS analysis demonstrated that MCF-7/Pac64 cells were smaller than MCF-7 cells with no difference in their granularity. Our results support the idea that paclitaxel induces apoptosis in a mitochondrial-dependent manner. Identifying breast cancer patients with a higher Bcl-2/Bax ratio and caspase 9 level and then inhibiting the activity of these proteins may improve the efficacy of chemotheraputic agents.

Keywords

References

  1. Bargou RC, Wagener C, Bommert K, et al (1996). Overexpression of the death-promoting gene Bax-alpha which is downregulated in breast cancer restores sensitivity to different apoptotic stimuli and reduces tumor growth in SCID mice. J Clin Invest, 97, 2651-9. https://doi.org/10.1172/JCI118715
  2. Carrick S, Parker S, Thornton CE, et al (2009). Single agent versus combination chemotherapy for metastatic breast cancer. Cochrane Database Syst Rev, 2, 3372.
  3. Childs AC, Phaneuf SL, Dirks AJ, et al (2002). Doxorubicin treatment in vivo causes cytochrome C release and cardiomyocyte apoptosis, as well as increased mitochondrial efficiency, superoxide dismutase activity, and Bcl-2:Bax ratio. Cancer Res, 62, 4592-8.
  4. Chinnaiyan AM (1999). The apoptosome: heart and soul of the cell death machine. Neoplasia, 1, 5-15. https://doi.org/10.1038/sj.neo.7900003
  5. Chipuk JE, Bouchier-Hayes L and Green DR (2006). Mitochondrial outer membrane permeabilization during apoptosis: the innocent bystander scenario. Cell Death Differ, 13, 1396-402. https://doi.org/10.1038/sj.cdd.4401963
  6. Chipuk JE, Moldoveanu T, Llambi F, et al (2010). The Bcl-2 family reunion. Mol Cell, 37, 299-310. https://doi.org/10.1016/j.molcel.2010.01.025
  7. Coley HM (2004). Development of drug-resistant models. Methods Mol Med, 88, 267-73.
  8. Crawford A and Nahta R (2011). Targeting Bcl-2 in herceptinresistant breast cancer cell lines. Curr Pharmacogenomics Person Med, 9, 184-90. https://doi.org/10.2174/187569211796957584
  9. Crotzer DR, Sun CC, Coleman RL, et al (2007). Lack of effective systemic therapy for recurrent clear cell carcinoma of the ovary. Gynecol Oncol, 105, 404-8. https://doi.org/10.1016/j.ygyno.2006.12.024
  10. Cryns V and Yuan J (1998). Proteases to die for. Genes Dev, 12, 1551-70. https://doi.org/10.1101/gad.12.11.1551
  11. Danial NN and Korsmeyer SJ (2004). Cell death: critical control points. Cell, 116, 205-19. https://doi.org/10.1016/S0092-8674(04)00046-7
  12. Darakhshan S, Bidmeshkipour A, Khazaei M, et al (2013). Synergistic effects of tamoxifen and tranilast on VEGF and MMP-9 regulation in cultured human breast cancer cells. Asian Pac J Cancer Prev, 14, 6869-74. https://doi.org/10.7314/APJCP.2013.14.11.6869
  13. Degterev A, Boyce M and Yuan J (2003). A decade of caspases. Oncogene, 22, 8543-67. https://doi.org/10.1038/sj.onc.1207107
  14. Ferreira KS, Kreutz C, Macnelly S, et al (2012). Caspase-3 feeds back on caspase-8, Bid and XIAP in type I Fas signaling in primary mouse hepatocytes. Apoptosis, 17, 503-15. https://doi.org/10.1007/s10495-011-0691-0
  15. Fulda S, Debatin KM (2006). Extrinsic versus intrinsic apoptosis pathways in anticancer chemotherapy. Oncogene, 25, 4798-811. https://doi.org/10.1038/sj.onc.1209608
  16. Gabizon A, Papahadjopoulos D (1988). Liposome formulations with prolonged circulation time in blood and enhanced uptake by tumors. Proc Natl Acad Sci USA, 85, 6949-53. https://doi.org/10.1073/pnas.85.18.6949
  17. Gabizon A, Price DC, Huberty J, et al (1990). Effect of liposome composition and other factors on the targeting of liposomes to experimental tumors: biodistribution and imaging studies. Cancer Res, 50, 6371-8.
  18. Gabizon AA (1992). Selective tumor localization and improved therapeutic index of anthracyclines encapsulated in longcirculating liposomes. Cancer Res, 52, 891-6.
  19. Garcia M, Jemal A, Ward E, et al (2007). Global cancer facts & figures 2007. Atlanta, GA: American cancer society, 1.
  20. Gee JM, Robertson JF, Ellis IO, et al (1994). Immunocytochemical localization of Bcl-2 protein in human breast cancers and its relationship to a series of prognostic markers and response to endocrine therapy. Int J Cancer, 59, 619-28. https://doi.org/10.1002/ijc.2910590508
  21. Ghanbari P, Mohseni M, Tabasinezhad M, et al (2014). Inhibition of survivin restores the sensitivity of breast cancer cells to docetaxel and vinblastine. Appl Biochem Biotechnol, 174, 667-81. https://doi.org/10.1007/s12010-014-1125-6
  22. Ghafouri-Fard S, Abdollahi DZ, Omrani M, et al (2012). shRNA mediated RHOXF1 silencing influences expression of BCL2 but not CASP8 in MCF-7 and MDA-MB-231 cell lines. Asian Pac J Cancer Prev, 13, 5865-9. https://doi.org/10.7314/APJCP.2012.13.11.5865
  23. Hamedeyazdan S, Fathiazad F, Sharifi S, et al (2012). Antiproliferative activity of Marrubium persicum extract in the MCF-7 human breast cancer cell line. Asian Pac J Cancer Prev, 13, 5843-8. https://doi.org/10.7314/APJCP.2012.13.11.5843
  24. Hembruff SL, Laberge ML, Villeneuve DJ, et al (2008). Role of drug transporters and drug accumulation in the temporal acquisition of drug resistance. BMC Cancer, 8, 318. https://doi.org/10.1186/1471-2407-8-318
  25. Iseri OD, Kars MD, Arpaci F, et al (2010). Gene expression analysis of drug-resistant MCF-7 cells: implications for relation to extracellular matrix proteins. Cancer Chemother Pharmacol, 65, 447-55. https://doi.org/10.1007/s00280-009-1048-z
  26. Janicke RU, Sprengart ML, Wati MR, et al (1998). Caspase-3 is required for DNA fragmentation and morphological changes associated with apoptosis. J Biol Chem, 273, 9357-60. https://doi.org/10.1074/jbc.273.16.9357
  27. Kelly PN and Strasser A (2011). The role of Bcl-2 and its prosurvival relatives in tumourigenesis and cancer therapy. Cell Death Differ, 18, 1414-24. https://doi.org/10.1038/cdd.2011.17
  28. Leung LK and Wang TT (1999). Differential effects of chemotherapeutic agents on the Bcl-2/Bax apoptosis pathway in human breast cancer cell line MCF-7. Breast Cancer Res Treat, 55, 73-83. https://doi.org/10.1023/A:1006190802590
  29. Lindsay J, Esposti MD and Gilmore AP (2011). Bcl-2 proteins and mitochondria--specificity in membrane targeting for death. Biochim Biophys Acta, 1813, 532-9. https://doi.org/10.1016/j.bbamcr.2010.10.017
  30. McDermott M, Eustace AJ, Busschots S, et al (2014). In vitro development of chemotherapy and targeted therapy drugresistant cancer cell lines: a practical guide with case studies. Front Oncol, 4, 40.
  31. Moulder S, Hortobagyi GN (2008). Advances in the treatment of breast cancer. Clin Pharmacol Ther, 83, 26-36. https://doi.org/10.1038/sj.clpt.6100449
  32. Ola MS, Nawaz M and Ahsan H (2011). Role of Bcl-2 family proteins and caspases in the regulation of apoptosis. Mol Cell Biochem, 351, 41-58. https://doi.org/10.1007/s11010-010-0709-x
  33. Olsson M and Zhivotovsky B (2011). Caspases and cancer. Cell Death Differ, 18, 1441-9. https://doi.org/10.1038/cdd.2011.30
  34. Oltvai ZN, Milliman CL and Korsmeyer SJ (1993). Bcl-2 heterodimerizes in vivo with a conserved homolog, Bax, that accelerates programmed cell death. Cell, 74, 609-19. https://doi.org/10.1016/0092-8674(93)90509-O
  35. Ouyang L, Shi Z, Zhao S, et al (2012). Programmed cell death pathways in cancer: a review of apoptosis, autophagy and programmed necrosis. Cell Prolif, 45, 487-98. https://doi.org/10.1111/j.1365-2184.2012.00845.x
  36. Parkin DM, Bray F, Ferlay J, et al (2005). Global cancer statistics, 2002. CA Cancer J Clin, 55, 74-108. https://doi.org/10.3322/canjclin.55.2.74
  37. Piche A, Grim J, Rancourt C, et al (1998). Modulation of Bcl-2 protein levels by an intracellular anti-Bcl-2 single-chain antibody increases drug-induced cytotoxicity in the breast cancer cell line MCF-7. Cancer Res, 58, 2134-40.
  38. Pommier Y, Sordet O, Antony S, et al (2004). Apoptosis defects and chemotherapy resistance: molecular interaction maps and networks. Oncogene, 23, 2934-49. https://doi.org/10.1038/sj.onc.1207515
  39. Rastogi RP, Sinha RP (2009). Apoptosis: molecular mechanisms and pathogenicity. EXCLI J, 8, 155-81.
  40. Reed JC (1998). Bcl-2 family proteins. Oncogene, 17, 3225-36.
  41. Ring AE and Ellis PA (2005). Taxanes in the treatment of early breast cancer. Cancer Treat Rev, 31, 618-27. https://doi.org/10.1016/j.ctrv.2005.09.005
  42. Sabzichi M, Hamishehkar H, Ramezani F, et al. (2014). Luteolinloaded phytosomes sensitize human breast carcinoma MDAMB 231 cells to doxorubicin by suppressing Nrf2 mediated signalling. Asian Pac J Cancer Prev, 15, 5311-6. https://doi.org/10.7314/APJCP.2014.15.13.5311
  43. Saloustros E, Mavroudis D, Georgoulias V (2008). Paclitaxel and docetaxel in the treatment of breast cancer. Expert Opin Pharmacother, 9, 2603-16. https://doi.org/10.1517/14656566.9.15.2603
  44. Scaffidi C, Fulda S, Srinivasan A, et al (1998). Two CD95 (APO-1/Fas) signaling pathways. EMBO J, 17, 1675-87. https://doi.org/10.1093/emboj/17.6.1675
  45. Schrohl AS, Meijer-van Gelder ME, Holten-Andersen MN, et al (2006). Primary tumor levels of tissue inhibitor of metalloproteinases-1 are predictive of resistance to chemotherapy in patients with metastatic breast cancer. Clin Cancer Res, 12, 7054-8. https://doi.org/10.1158/1078-0432.CCR-06-0950
  46. Seifi-Alan M, Shamsi R, Ghafouri-Fard S, et al (2013). Expression analysis of two cancer-testis genes, FBXO39 and TDRD4, in breast cancer tissues and cell lines. Asian Pac J Cancer Prev, 14, 6625-9. https://doi.org/10.7314/APJCP.2013.14.11.6625
  47. Seve P, Isaac S, Tredan O, et al (2005). Expression of class III {beta}-tubulin is predictive of patient outcome in patients with non-small cell lung cancer receiving vinorelbine-based chemotherapy. Clin Cancer Res, 11, 5481-6. https://doi.org/10.1158/1078-0432.CCR-05-0285
  48. Shajahan AN, Dobbin ZC, Hickman FE, et al (2012). Tyrosinephosphorylated caveolin-1 (Tyr-14) increases sensitivity to paclitaxel by inhibiting BCL2 and BCLxL proteins via c-Jun N-terminal kinase (JNK). J Biol Chem, 287, 17682-92. https://doi.org/10.1074/jbc.M111.304022
  49. Simstein R, Burow M, Parker A, et al (2003). Apoptosis, chemoresistance, and breast cancer: insights from the MCF-7 cell model system. Exp Biol Med (Maywood), 228, 995-1003.
  50. Stoetzer OJ, Nussler V, Darsow M, et al (1996). Association of Bcl-2, Bax, bcl-xL and interleukin-1 beta-converting enzyme expression with initial response to chemotherapy in acute myeloid leukemia. Leukemia, 10, 18-22.
  51. Strasser A, Harris AW, Huang DC, et al (1995). Bcl-2 and Fas/APO-1 regulate distinct pathways to lymphocyte apoptosis. EMBO J, 14, 6136-47.
  52. Tabasinezhad M, Samadi N, Ghanbari P, et al (2013). Sphingosin 1-phosphate contributes in tumor progression. J Cancer Res Ther, 9, 556-63. https://doi.org/10.4103/0973-1482.126446
  53. Tang D, Lahti JM, Kidd VJ (2000). Caspase-8 activation and bid cleavage contribute to MCF7 cellular execution in a caspase-3-dependent manner during staurosporine-mediated apoptosis. J Biol Chem, 275, 9303-7. https://doi.org/10.1074/jbc.275.13.9303
  54. Thornberry NA, Lazebnik Y (1998). Caspases: enemies within. Science, 281, 1312-6. https://doi.org/10.1126/science.281.5381.1312
  55. Wang H, Vo T, Hajar A, et al (2014). Multiple mechanisms underlying acquired resistance to taxanes in selected docetaxel-resistant MCF-7 breast cancer cells. BMC Cancer, 14, 37. https://doi.org/10.1186/1471-2407-14-37
  56. Ward S, Simpson E, Davis S, et al (2007). Taxanes for the adjuvant treatment of early breast cancer: systematic review and economic evaluation. Health Technol Assess, 11, 1-144.
  57. Wild PJ, Reichle A, Andreesen R, et al (2004). Microsatellite instability predicts poor short-term survival in patients with advanced breast cancer after high-dose chemotherapy and autologous stem-cell transplantation. Clin Cancer Res, 10, 556-64. https://doi.org/10.1158/1078-0432.CCR-0601-03
  58. Yang E and Korsmeyer SJ (1996). Molecular thanatopsis: a discourse on the BCL2 family and cell death. Blood, 88, 386-401.
  59. Zuo KQ, Zhang XP, Zou J, et al (2010). Establishment of a paclitaxel resistant human breast cancer cell strain (MCF-7/Taxol) and intracellular paclitaxel binding protein analysis. J Int Med Res, 38, 1428-35. https://doi.org/10.1177/147323001003800424

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