GPX4
脂质过氧化
癌症
程序性细胞死亡
癌症研究
病态的
癌细胞
医学
细胞生物学
细胞凋亡
生物
神经科学
化学
氧化应激
生物化学
病理
内科学
过氧化氢酶
谷胱甘肽过氧化物酶
作者
Magali Walravens,Ine Koeken,Tom Vanden Berghe
出处
期刊:Biochemical Society Transactions
[Portland Press]
日期:2024-04-17
卷期号:52 (2): 693-706
摘要
Pathological breakdown of membrane lipids through excessive lipid peroxidation (LPO) was first described in the mid-20th century and is now recognized as a form of regulated cell death, dubbed ferroptosis. Accumulating evidence unveils how metabolic regulation restrains peroxidation of phospholipids within cellular membranes, thereby impeding ferroptosis execution. Unleashing these metabolic breaks is currently therapeutically explored to sensitize cancers to ferroptosis inducing anti-cancer therapies. Reversely, these natural ferroptotic defense mechanisms can fail resulting in pathological conditions or diseases such as ischemia-reperfusion injury, multi-organ dysfunction, stroke, infarction, or neurodegenerative diseases. This minireview outlines current ferroptosis-inducing anti-cancer strategies and highlights the detection as well as the therapeutic targeting of ferroptosis in preclinical experimental settings. Herein, we also briefly summarize observations related to LPO, iron and redox deregulation in patients that might hint towards ferroptosis as a contributing factor.
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