脂质过氧化
GPX4
细胞生物学
转录因子
氧化应激
4-羟基壬醛
程序性细胞死亡
信号转导
化学
生物
活性氧
细胞凋亡
生物化学
基因
超氧化物歧化酶
谷胱甘肽过氧化物酶
作者
Matthew Dodson,Raúl Castro-Portuguez,Donna D. Zhang
出处
期刊:Redox biology
[Elsevier]
日期:2019-01-12
卷期号:23: 101107-101107
被引量:1276
标识
DOI:10.1016/j.redox.2019.101107
摘要
The transcription factor nuclear factor erythroid 2-related factor 2 (NRF2) is a key regulator of the cellular antioxidant response, controlling the expression of genes that counteract oxidative and electrophilic stresses. Many pathological conditions are linked to imbalances in redox homeostasis, illustrating the important role of antioxidant defense systems in preventing the pathogenic effects associated with the accumulation of reactive species. In particular, it is becoming increasingly apparent that the accumulation of lipid peroxides has an important role in driving the pathogenesis of multiple disease states. A key example of this is the recent discovery of a novel form of cell death termed ferroptosis. Ferroptosis is an iron-dependent, lipid peroxidation-driven cell death cascade that has become a key target in the development of anti-cancer therapies, as well as the prevention of neurodegenerative and cardiovascular diseases. In this review, we will provide a brief overview of lipid peroxidation, as well as key components involved in the ferroptotic cascade. We will also highlight the role of the NRF2 signaling pathway in mediating lipid peroxidation and ferroptosis, focusing on established NRF2 target genes that mitigate these pathways, as well as the relevance of the NRF2-lipid peroxidation-ferroptosis axis in disease.
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