脂肪性肝炎
程序性细胞死亡
GPX4
脂肪肝
医学
生物信息学
生物
细胞凋亡
癌症研究
疾病
氧化应激
病理
内科学
遗传学
谷胱甘肽过氧化物酶
过氧化氢酶
作者
Yifei Le,Zhijie Zhang,Cui Wang,Dezhao Lu
出处
期刊:Endocrine, metabolic & immune disorders
[Bentham Science Publishers]
日期:2021-05-01
卷期号:21 (5): 785-800
被引量:15
标识
DOI:10.2174/1871530320666200731175328
摘要
Cell death is a fundamental biological phenomenon that contributes to the pathogenesis of various diseases. Regulation of iron and iron metabolism has received considerable research interests especially concerning the progression of metabolic diseases.Emerging evidence shows that ferroptosis, a non-apoptotic programmed cell death induced by iron-dependent lipid peroxidation, contributes to the development of complex diseases such as non-alcoholic steatohepatitis, cardiomyopathy, renal ischemia-reperfusion, and neurodegenerative diseases. Therefore, inhibiting ferroptosis can improve the pathophysiology of associated metabolic diseases. This review describes the vital role of ferroptosis in mediating the development of certain metabolic diseases. Besides, the potential risk of iron and ferroptosis in atherosclerosis and cardiovascular diseases is also described. Iron overload and ferroptosis are potential secondary causes of death in metabolic diseases. Moreover, this review also provides potential novel approaches against ferroptosis based on recent research advances.Several controversies exist concerning mechanisms underlying ferroptotic cell death in metabolic diseases, particularly in atherosclerosis. Since ferroptosis participates in the progression of metabolic diseases such as non-alcoholic steatohepatitis (NASH), there is a need to develop new drugs targeting ferroptosis to alleviate such diseases.
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