上睑下垂
坏死性下垂
心肌病
程序性细胞死亡
自噬
医学
心脏毒性
GPX4
发病机制
氧化应激
心力衰竭
细胞凋亡
癌症研究
神经科学
生物
免疫学
心脏病学
内科学
遗传学
化疗
谷胱甘肽过氧化物酶
过氧化氢酶
作者
Ning Li,Wenyang Jiang,Wei Wang,Rui Xiong,Xiaojing Wu,Qing Geng
标识
DOI:10.1016/j.phrs.2021.105466
摘要
Ferroptosis is a new form of regulated cell death (RCD) driven by iron-dependent lipid peroxidation, which is morphologically and mechanistically distinct from other forms of RCD including apoptosis, autophagic cell death, pyroptosis and necroptosis. Recently, ferroptosis has been found to participate in the development of various cardiovascular diseases (CVDs) including doxorubicin-induced cardiotoxicity, ischemia/reperfusion-induced cardiomyopathy, heart failure, aortic dissection and stroke. Cardiovascular homeostasis is indulged in delicate equilibrium of assorted cell types composing the heart or vessels, and how ferroptosis contributes to the pathophysiological responses in CVD progression is unclear. Herein, we reviewed recent discoveries on the basis of ferroptosis and its involvement in CVD pathogenesis, together with related therapeutic potentials, aiming to provide insights on fundamental mechanisms of ferroptosis and implications in CVDs and associated disorders.
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