Expression of calbindin-D28k is inversely correlated with proapototic gene expression in hydrogen peroxide-induced cell death in endometrial cancer cells

被引:12
|
作者
Jung, Eui-Man [1 ]
Choi, Kyung-Chul [1 ]
Jeung, Eui-Bae [1 ]
机构
[1] Chungbuk Natl Univ, Coll Vet Med, Lab Vet Biochem & Mol Biol, Cheongju 361763, Chungbuk, South Korea
关键词
calbindin-D(28)k; Bax; p53; Bcl-2; caspase; 3; apoptosis; TUMOR-SUPPRESSOR P53; PITUITARY GH3 CELLS; ENDOPLASMIC-RETICULUM; INDUCED APOPTOSIS; OXIDATIVE STRESS; PROGESTERONE-RECEPTOR; SUPEROXIDE-DISMUTASE; MENSTRUAL-CYCLE; KEY MEDIATORS; CA2+ CHANNEL;
D O I
10.3892/ijo.2011.916
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Calbindin-D-28k (CaBP-28k) is a calcium binding protein important for intracellular Ca2+ buffering and known to have anti-apoptotic properties in neurons, osteoblasts and male germ cells. Although endometrial cancer is a common invasive gynecologic malignancy, the involvement of uterine CaBP-28k in apoptotic signaling of endometrial cancer is poorly understood. The present study investigates the role of CaBP-28k in hydrogen peroxide (H2O2)-induced apoptotic signaling in human enclometrial Ishikawa cells. The dose- and time-dependent effect of H2O2 on Bax, p53 and Bcl-2 expression was assessed by Western blot analysis. Treatment of cells with 1 mM H2O2 for 1 h induced an increase in Bax and p53 expression, but the expression of Bcl-2 was not affected by H2O2, treatment. Interestingly, overexpression of CaBP- 28k inhibited cell death and caused a decrease in Bax, p53 and caspase 3 expression during H2O2-induced apoptosis, suggesting that CaBP-28k blocks the up-regulation of apoptosis-related gene expression. siRNA knockdown of CaBP-28k resulted in an elevation of H2O2-induced cell death and an increase in Bax, p53 and caspase 3, providing additional evidence that induction of the CaBP-28k gene might be associated with survival signaling during H2O2-mediated cell death. Overall, these results suggest that CaBP-28k expression is inversely correlated with pro-apoptotic gene expression in human endometrial Ishikawa cells.
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页码:1059 / 1066
页数:8
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