Ferrootosis: Death by Lipid Peroxidation

被引:2243
作者
Yang, Wan Seok [1 ,4 ]
Stockwell, Brent R. [1 ,2 ,3 ]
机构
[1] Columbia Univ, Howard Hughes Med Inst, Dept Biol Sci, New York, NY 10032 USA
[2] Columbia Univ, Dept Chem, New York, NY 10027 USA
[3] Columbia Univ, Dept Syst Biol, New York, NY USA
[4] St Johns Univ, Dept Biol Sci, Queens, NY USA
基金
美国国家卫生研究院;
关键词
NONAPOPTOTIC CELL-DEATH; HEPATOCELLULAR-CARCINOMA CELLS; STRESS-INDUCED APOPTOSIS; OXIDATIVE STRESS; SPONDYLOMETAPHYSEAL DYSPLASIA; HUNTINGTONS-DISEASE; LYMPHOMA GROWTH; TUMOR-CELLS; SBP2; GENE; FERROPTOSIS;
D O I
10.1016/j.tcb.2015.10.014
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Ferroptosis is a regulated form of cell death driven by loss of activity of the lipid repair enzyme glutathione peroxidase 4 (GPX4) and subsequent accumulation of lipid -based reactive oxygen species (ROS), particularly lipid hydroperoxides. This form of iron -dependent cell death is genetically, biochemically, and morphologically distinct from other cell death modalities, including apoptosis, unregulated necrosis, and necroptosis. Ferroptosis is regulated by specific pathways and is involved in diverse biological contexts. Here we summarize the discovery of ferroptosis, the mechanism of ferroptosis regulation, and its increasingly appreciated relevance to both normal and pathological physiology.
引用
收藏
页码:165 / 176
页数:12
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