Molecular mechanism of 'mitocan'-induced apoptosis in cancer cells epitomizes the multiple roles of reactive oxygen species and Bcl-2 family proteins

被引:179
作者
Neuzil, Jiri
Wang, Xiu-Fang
Dong, Lan-Feng
Low, Pauline
Ralph, Stephen J.
机构
[1] Griffith Univ, Sch Med Sci, Apoptosis Res Grp, Southport, Qld 9716, Australia
[2] Acad Sci Czech Republ, Inst Mol Genet, Prague, Czech Republic
[3] Griffith Univ, Sch Med Sci, Genom Res Ctr, Southport, Qld 9716, Australia
来源
FEBS LETTERS | 2006年 / 580卷 / 22期
关键词
mitocan; alpha-tocopheryl succinate; reactive oxygen species; Bax; Bcl-2/Bcl-X-L; BH3; domain; cardiolipin; cytochrome c;
D O I
10.1016/j.febslet.2006.05.072
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
Mitochondria have emerged recently as effective targets for novel anti-cancer drugs referred to as 'mitocans'. We propose that the molecular mechanism of induction of apoptosis by mitocans, as exemplified by the drug alpha-tocopheryl succinate, involves generation of reactive oxygen species (ROS). ROS then mediate the formation of disufide bridges between cytosolic Bax monomers, resulting in the formation of mitochondrial outer membrane channels. ROS also cause oxidation of cardiolipin, triggering the release of cytochrome c and its translocation via the activated Bax channels. This model may provide a general mechanism for the action of inducers of apoptosis and anticancer drugs, mitocans, targeting mitochondria via ROS production. (c) 2006 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:5125 / 5129
页数:5
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