The role of the electron transport gene SDHC on lifespan and cancer

被引:17
作者
Ishii, Naoaki [1 ]
Ishii, Takamasa
Hartman, Philip S.
机构
[1] Tokai Univ, Sch Med, Dept Mol Life Sci, Kanagawa 2591193, Japan
[2] Texas Christian Univ, Dept Biol, Ft Worth, TX 76129 USA
关键词
aging; cancer; mitochondria; electron transport chain; oxidative stress; SDHC;
D O I
10.1016/j.exger.2006.06.037
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
Much attention has been focused on the hypothesis that oxidative damage contributes to cellular and organismal aging. A mev-1 mutation in the cytochrome b large subunit (SDHC) of complex II results in superoxide anion (O-2(-)) overproduction and therefore leads to apoptosis and precocious aging in the nematode Caenorhabditis elegans. To extend these data, a transgenic mouse cell line was constructed with a homologous mutation to mev-1. Many of the mutant nematode phenotypes (e.g., increased superoxide anion production, apoptosis) were recapitulated in the mouse. In addition, a significant fraction of the cells that survived apoptosis were transformed. These data support the notion that oxidative stress from mitochondria play an important role of both apoptosis, which leads to precocious aging, and cancer (c) 2006 Elsevier Inc. All rights reserved.
引用
收藏
页码:952 / 956
页数:5
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