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Oleanolic acid 3-acetate, a minor element of ginsenosides, induces apoptotic cell death in ovarian carcinoma and endometrial carcinoma cells via the involvement of a reactive oxygen species-independent mitochondrial pathway

  • Jo, Hantae (Department of Biological Sciences, Ajou University) ;
  • Oh, Jeong-Hyun (Oncology Business Unit, MSD-Korea) ;
  • Park, Dong-Wook (Laboratory of Reproductive Medicine, Cheil General Hospital & Women's Healthcare Center, College of Medicine, Dankook University) ;
  • Lee, Changho (Department of Pharmacology and Biomedical Science, College of Medicine, Hanyang University) ;
  • Min, Churl K. (Department of Biological Sciences, Ajou University)
  • Received : 2018.05.25
  • Accepted : 2018.09.13
  • Published : 2020.01.15

Abstract

Objectives: Oleanolic acid, a minor element of ginsenosides, and its derivatives have been shown to have cytotoxicity against some tumor cells. The impact of cytotoxic effect of oleanolic acid 3-acetate on ovarian cancer SKOV3 cells and endometrial cancer HEC-1A cells were examined both in vivo and in vitro to explore the underlying mechanisms. Methods: Cytotoxic effects of oleanolic acid 3-acetate were assessed by cell viability, phosphatidylserine exposure on the cell surface, mitochondrial release of cytochrome C, nuclear translocation of apoptosis-inducing factor, depolarization of mitochondrial transmembrane potential (∆Ψm), and generation of reactive oxygen species (ROS). In vivo inhibition of tumor growth was also assessed with xenografts in immunocompromised mice. Results: Oleanolic acid 3-acetate exhibited potent cytotoxicity toward SKOV3 and HEC-1A cells by decreasing cell viability in a concentration-dependent manner. Importantly, oleanolic acid 3-acetate effectively suppressed the growth of SKOV3 cell tumor xenografts in immunocompromised mice. Furthermore, oleanolic acid 3-acetate induced apoptotic cell death as revealed by loss of ∆Ψm, release of cytochrome c, and nuclear translocation of apoptosis-inducing factor with a concomitant activation of many proapoptotic cellular components including poly(ADP-ribose) polymerase, Bcl-2, and caspases-8, caspase-3, and caspase-7. Oleanolic acid 3-acetate, however, caused a decrease in ROS production, suggesting the involvement of an ROS-independent pathway in oleanolic acid 3-acetate-induced apoptosis in SKOV3 and HEC-1A cells. Conclusion: These findings support the notion that oleanolic acid 3-acetate could be used as a potent anticancer supplementary agent against ovarian and endometrial cancer. Oleanolic acid 3-acetate exerts its proapoptotic effects through a rather unique molecular mechanism that involves an unconventional ROS-independent but mitochondria-mediated pathway.

Keywords

References

  1. Hill RA, Connolly JD. Triterpenoids. Nat Prod Rep 2011;28:1087-117. https://doi.org/10.1039/c1np00012h
  2. Liby KT, Yore MM, Sporn MB. Triterpenoids and rexinoids as multifunctional agents for the prevention and treatment of cancer. Nat Rev Cancer 2007;7:357-69. https://doi.org/10.1038/nrc2129
  3. Bray F, Jemal A, Grey N, Ferlay J, Forman D. Global cancer transitions according to the Human Development Index (2008-2030): a population-based study. Lancet Oncol 2012;13:709-801.
  4. Bolton KL. Role of common genetic variants in ovarian cancer susceptibility and outcome. J Intern Med 2012:1365-2796.
  5. Sjoblom T, Jones S, Wood LD, Parsons DW, Lin J, Barber TD, Mandelker D, Leary RJ, Ptak J, Sillman N, et al. The consensus coding sequences of human breast and colorectal cancers. Science 2006;314:268-74. https://doi.org/10.1126/science.1133427
  6. Loeb LA. Human cancers express mutator phenotypes: origin, consequences and targeting. Nat Rev Cancer 2011;11:450-7. https://doi.org/10.1038/nrc3063
  7. Jutooru I, Chadalapaka G, Abdelrahim M, Basha MR, Samudio I, Konopleva M, Andreeff M, Safe S. Methyl 2-cyano-3,12-dioxooleana-1,9-dien-28-oate decreases specificity protein transcription factors and inhibits pancreatic tumor growth: role of microRNA-27a. Mol Pharmacol 2010;78(2):226-36. https://doi.org/10.1124/mol.110.064451
  8. Park WH, Lee MS, Park K, Kim ES, Kim BK, Lee YY. Monensin-mediated growth inhibition in acute myelogenous leukemia cells via cell cycle arrest and apoptosis. Int J Cancer 2001;101:235-42. https://doi.org/10.1002/ijc.10592
  9. Lin HI, Lee YJ, Chen BF, Tsai MC, Lu JL, Chou CJ, Jow GM. Involvement of Bcl-2 family, cytochrome c and caspase 3 in induction of apoptosis by beauvericin in human non-small cell lung cancer cells. Cancer Lett 2005;230:248-59. https://doi.org/10.1016/j.canlet.2004.12.044
  10. Campos CB, Degasperi GR, Pacifico DS, Alberici LC, Carreira RS, Guimaraes F, Castilho RF, Vercesi AE. Ibuprofen-induced Walker 256 tumor cell death: cytochrome c release from functional mitochondria and enhancement by calcineurin inhibition. Biochem Pharmacol 2004;68:2197-206. https://doi.org/10.1016/j.bcp.2004.08.006
  11. Hu S, Zhao H, Al-Humadi NH, Yin XJ, Ma JK. Silica-induced apoptosis in alveolar macrophages: evidence of in vivo thiol depletion and the activation of mitochondrial pathway. J Toxicol Environ Health 2006;69:1261-84. https://doi.org/10.1080/15287390500361875
  12. Arimura T, Kojima-Yuasa A, Kennedy DO, Matsui-Yuasa I. Reactive oxygen species-independent G1 arrest induced by evening primrose extract in Ehrlich ascites tumor cells. Cancer Lett 2004;207:19-25. https://doi.org/10.1016/j.canlet.2003.11.001
  13. Ko CH, Shen SC, Hsu CS, Chen YC. Mitochondrial-dependent, reactive oxygen species-independent apoptosis by myricetin: roles of protein kinase C, cytochrome c, and caspase cascade. Biochem Pharmacol 2005;69:913-27. https://doi.org/10.1016/j.bcp.2004.12.005
  14. Flynn JM, Cammarata PR. Estradiol attenuates mitochondrial depolarization in polyol-stressed lens epithelial cells. Mol Vis 2006;12:271-82.
  15. Park DW, Choi DS, Ryu H-S, Kwon HC, Joo H, Min CK. A well-defined in vitro three-dimensional culture of human endometrium and its applicability to endometrial cancer invasion. Cancer Lett 2003;195:185-92. https://doi.org/10.1016/S0304-3835(03)00131-9
  16. Choi DS, Kim JH, Ryu HS, Kim HC, Han JH, Lee JS, Min CK. Syndecan-1, a key regulator of cell viability in endometrial cancer. Int J Cancer 2007;121:741-50. https://doi.org/10.1002/ijc.22713
  17. Park DW, Cho T, Kim MR, Kim YA, Min CK, Hwang KJ. ATP-induced apoptosis of human granulosa luteal cells cultured in vitro. Fertil Steril 2003;80:993-1002. https://doi.org/10.1016/S0015-0282(03)01118-X
  18. Oh JH, Lee HS, Park SH, Ryu HS, Min CK. Syndecan-1 overexpression promotes tumor growth and angiogenesis in an endometrial cancer xenograft model. Int J Gynecol Cancer 2010;20:751-6. https://doi.org/10.1111/IGC.0b013e3181e02faa
  19. Mendel DB, Laird AD, Xin X, Louie SG, Christensen JG, Li G, Schreck RE, Abrams TJ, Ngai TJ, Lee LB, et al. In vivo antitumor activity of SU11248, a novel tyrosine kinase inhibitor targeting vascular endothelial growth factor and platelet derived growth factor receptors: determination of a pharmacokinetic/pharmacodynamic relationship. Clin Cancer Res 2003;9:327-37.
  20. Joza N, Susin SA, Daugas E, Stanford WL, Cho SK, Li CYJ, Sasaki T, Elia AJ, Cheng HYM, Ravagnan L, et al. Essential role of the mitochondrial apoptosisinducing factor in programmed cell death. Nature 2001;410:549-54. https://doi.org/10.1038/35069004
  21. Wang XH, Jia DZ, Liang YJ, Yan SL, Ding Y, Chen LM, Shi Z, Zeng MS, Liu GF, Fu LW. Lgf-YL-9 induces apoptosis in human epidermoid carcinoma KB cells and multidrug resistant KBv200 cells via reactive oxygen species-independent mitochondrial pathway. Cancer Lett 2007;249:256-70. https://doi.org/10.1016/j.canlet.2006.09.008
  22. Park DS, Morris EJ, Stefanis L, Troy CM, Shelanski ML, Geller HM, Greene LA. Multiple pathways of neuronal death induced by DNA-damaging agents, NGF deprivation, and oxidative stress. J Neurosci 1998;18:830-40. https://doi.org/10.1523/jneurosci.18-03-00830.1998
  23. Lambert DG. Drugs and receptors. Contin Edu Anesth Crit Care Pain 2004;4:181-4. https://doi.org/10.1093/bjaceaccp/mkh049
  24. Pae HO, Oh GS, Choi BM, Seo EA, Oh H, Shin MK, Kim TH, Kwon TO, Chung HT. Induction of apoptosis by 4-acetyl-12,13-epoxyl-9-trichothecene-3,15-diol from Isaria japonica Yasuda through intracellular reactive oxygen species formation and caspase-3 activation in human leukemia HL-60 cells. Toxicol In Vitro 2003;17:49-57. https://doi.org/10.1016/S0887-2333(02)00097-8
  25. Zhuge J, Cederbaum AI. Serum deprivation-induced HepG2 cell death is potentiated by CYP2E1. Free Radic Biol Med 2006;40:63-74. https://doi.org/10.1016/j.freeradbiomed.2005.08.012

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