Arsenic trioxide induces gallbladder carcinoma cell apoptosis via downregulation of Bcl-2

被引:38
|
作者
Ai, Zhilong [1 ]
Lu, Weiqi [1 ]
Qin, Xinyu [1 ]
机构
[1] Fudan Univ, Zhongshan Hosp, Shanghai 200032, Peoples R China
关键词
gallbladder carcinoma; arsenic trioxide; apoptosis; AKT; Bcl-2; in vitro;
D O I
10.1016/j.bbrc.2006.07.181
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
Gallbladder carcinoma (GBC), an aggressive and mostly lethal malignancy, is known to be resistant to a number of apoplotic stimuli. Here, we report for the first time the pro-apoptosis role of arsenic trioxide (AS(2)O(3)) in gallbladder carcinoma and identify the contribution of Bcl-2 in the AS(2)O(3)-induced apoptosis. The treatment of AS(2)O(3) in gallbladder carcinoma cells could induce apoptosis in a dose-dependent manner and downregulate the expression of anti-apoptotic protein Bcl-2 at mRNA level. Moreover, Bcl-2 overexpression could protect gallbladder carcinoma cells from As2O3-induced apoptosis, indicating the contribution of Bcl-2 in AS(2)O(3)-induced apoptosis. Taken together, these results suggest that arsenic trioxide induces gallbladder carcinoma cell apoptosis via downregulation of Bcl-2, which may have important therapeutic implications in gallbladder carcinoma patients. (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:1075 / 1081
页数:7
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