P73 regulates cisplatin-induced apoptosis in ovarian cancer cells via a calcium/calpain-dependent mechanism

被引:67
作者
Al-Bahlani, S. [1 ,2 ,3 ,4 ]
Fraser, M. [1 ,2 ,3 ,9 ,10 ]
Wong, A. Y. C. [2 ,5 ]
Sayan, B. S. [6 ]
Bergeron, R. [2 ,5 ,7 ]
Melino, G. [6 ,8 ]
Tsang, B. K. [1 ,2 ,7 ,11 ]
机构
[1] Univ Ottawa, Ottawa Hosp, Res Inst, Dept Obstet & Gynaecol, Ottawa, ON K1Y 4E9, Canada
[2] Univ Ottawa, Ottawa Hosp, Res Inst, Dept Cellular & Mol Med, Ottawa, ON K1Y 4E9, Canada
[3] Ottawa Hosp, Res Inst, Chron Dis Program, Ottawa, ON, Canada
[4] Sultan Qaboos Univ, Dept Pathol, Muscat, Oman
[5] Ottawa Hosp, Res Inst, Neurosci Program, Ottawa, ON, Canada
[6] Univ Leicester, MRC, Toxicol Unit, Leicester, Leics, England
[7] Univ Ottawa, Dept Psychiat, Ottawa, ON K1N 6N5, Canada
[8] Univ Rome, Dept Expt Med, IDI IRCCS Biochem Lab, Rome, Italy
[9] Princess Margaret Hosp, Ontario Canc Inst, Radiat Med Program, Toronto, ON M4X 1K9, Canada
[10] Princess Margaret Hosp, Ontario Canc Inst, STTARR Innovat Facil, Toronto, ON M4X 1K9, Canada
[11] Seoul Natl Univ, World Class Univ WCU Biomodulat Major, Dept Agr Biotechnol, Coll Agr & Life Sci, Seoul, South Korea
基金
新加坡国家研究基金会; 英国医学研究理事会;
关键词
CDDP; p73; alpha; calpain; calcium; ovarian cancer; X-LINKED INHIBITOR; P53; FAMILY; NEUROBLASTOMA-CELLS; CARCINOMA CELLS; FEEDBACK LOOP; IN-VIVO; CALPAIN; PROTEIN; BAX; CHEMOSENSITIVITY;
D O I
10.1038/onc.2011.134
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
P73 is important in drug-induced apoptosis in some cancer cells, yet its role in the regulation of chemosensitivity in ovarian cancer (OVCA) is poorly understood. Furthermore, if and how the deregulation of p73-mediated apoptosis confers resistance to cisplatin (CDDP) treatment is unclear. Here we demonstrate that TAp73 alpha over-expression enhanced CDDP-induced PARP cleavage and apoptosis in both chemosensitive (OV2008 and A2780s) and their resistant counterparts (C13* and A2780cp) and another chemoresistant OVCA cells (Hey); in contrast, the effect of Delta Np73 alpha over-expression was variable. P73 alpha downregulation attenuated CDDP-induced PUMA and NOXA upregulation and apoptosis in OV2008 cells. CDDP decreased p73 alpha steady-state protein levels in OV2008, but not in C13*, although the mRNA expression was identical. CDDP-induced p73 alpha downregulation was mediated by a calpain-dependent pathway. CDDP induced calpain activation and enhanced its cytoplasmic interaction and co-localization with p73 alpha in OV2008, but not C13* cells. CDDP increased the intracellular calcium concentration ([Ca(2+)](i)) in OV2008 but not C13* whereas cyclopiazonic acid (CPA), a Ca(2+)-ATPase inhibitor, caused this response and calpain activation, p73 alpha processing and apoptosis in both cell types. CDDP-induced [Ca(2+)](i) increase in OV2008 cells was not effected by the elimination of extracellular Ca(2+), but this was attenuated by the depletion of internal Ca(2+) store, indicating that mobilization of intracellular Ca(2+1) stores was potentially involved. These findings demonstrate that p73 alpha and its regulation by the Ca(2+)-mediated calpain pathway are involved in CDDP-induced apoptosis in OVCA cells and that dysregulation of Ca(2+)/calpain/p73 signaling may in part be the pathophysiology of CDDP resistance. Understanding the cellular and molecular mechanisms of chemoresistance will direct the development of effective strategies for the treatment of chemoresistant OVCA. Oncogene (2011) 30, 4219-4230; doi: 10.1038/onc.2011.134; published online 25 April 2011
引用
收藏
页码:4219 / 4230
页数:12
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