Ferroptotic Cell Death: New Regulatory Mechanisms for Metabolic Diseases

被引:28
|
作者
Le, Yifei [1 ]
Zhang, Zhijie [1 ]
Wang, Cui [1 ]
Lu, Dezhao [1 ]
机构
[1] Zhejiang Chinese Med Univ, Coll Life Sci, POB 310053, Hangzhou, Peoples R China
关键词
Ferroptosis; iron; atherosclerosis; non-alcoholic steatohepatitis; cardiomyopathy; metabolism; FATTY LIVER-DISEASE; TRANSFERRIN-BOUND IRON; FRIEDREICH ATAXIA; NONALCOHOLIC STEATOHEPATITIS; HEPATIC FERROPTOSIS; GLUCOSE-HOMEOSTASIS; OXIDATIVE STRESS; ACTIVATION; MACROPHAGES; BINDING;
D O I
10.2174/1871530320666200731175328
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: 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. Discussion: 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. Conclusion: 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.
引用
收藏
页码:785 / 800
页数:16
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