Ferroptotic Cell Death: New Regulatory Mechanisms for Metabolic Diseases

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]
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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