GPX4
脂质过氧化
程序性细胞死亡
神经退行性变
化学
坏死性下垂
氧化应激
细胞生物学
谷胱甘肽
活性氧
医学
线粒体
生物化学
自噬
细胞凋亡
癌症研究
生物
谷胱甘肽过氧化物酶
超氧化物歧化酶
疾病
内科学
作者
Sebastian Doll,Marcus Conrad
出处
期刊:Iubmb Life
[Wiley]
日期:2017-03-09
卷期号:69 (6): 423-434
被引量:300
摘要
Ferroptosis is a recently described form of regulated necrotic cell death, which appears to contribute to a number of diseases, such as tissue ischemia/reperfusion injury, acute renal failure, and neurodegeneration. A hallmark of ferroptosis is iron-dependent lipid peroxidation, which can be inhibited by the key ferroptosis regulator glutathione peroxidase 4(Gpx4), radical trapping antioxidants and ferroptosis-specific inhibitors, such as ferrostatins and liproxstatins, as well as iron chelation. Although great strides have been made towards a better understanding of the proximate signals of distinctive lipid peroxides in ferroptosis, still little is known about the mechanistic implication of iron in the ferroptotic process. Hence, this review aims at summarizing recent advances in our understanding to what is known about enzymatic and nonenzymatic routes of lipid peroxidation, the involvement of iron in this process and the identification of novel players in ferroptotic cell death. Additionally, we review early works carried out long time before the term "ferroptosis" was actually introduced but which were instrumental in a better understanding of the role of ferroptosis in physiological and pathophysiological contexts. © 2017 IUBMB Life, 69(6):423-434, 2017.
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