Role of BAX in the apoptotic response to anticancer agents

被引:772
作者
Zhang, L
Yu, J
Park, BH
Kinzler, KW
Vogelstein, B [1 ]
机构
[1] Johns Hopkins Univ, Sch Med, Howard Hughes Med Inst, Ctr Oncol, Baltimore, MD 21231 USA
[2] Johns Hopkins Univ, Sch Med, Program Human Genet, Baltimore, MD 21231 USA
关键词
D O I
10.1126/science.290.5493.989
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
To assess the role of BAX in drug-induced apoptosis in human colorectal cancer cells, we generated cells that Lack functional BAX genes. Such cells were partially resistant to the apoptotic effects of the chemotherapeutic agent 5-fluorouracil, but apoptosis was not abolished. In contrast, the absence of BAX completely abolished the apoptotic response to the chemopreventive agent sulindac and other nonsteroidal anti-inflammatory drugs (NSAIDs). NSAIDs inhibited the expression of the antiapoptotic protein Bcl-X-L, resulting in an altered ratio of BAX to BcL-X-L and subsequent mitochondria-mediated cell death. These results establish an unambiguous role for BAX in apoptotic processes in human epithelial cancers and may have implications for cancer chemoprevention strategies.
引用
收藏
页码:989 / +
页数:5
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