自噬
GPX4
程序性细胞死亡
细胞生物学
活性氧
细胞凋亡
生物
脂质过氧化
氧化应激
生物化学
超氧化物歧化酶
谷胱甘肽过氧化物酶
作者
Seung-Hee Lee,Narae Hwang,Byeong Geun Seok,Sangguk Lee,Seon‐Jin Lee,Su Wol Chung
标识
DOI:10.1038/s41419-023-05978-8
摘要
Ferroptosis, a programmed cell death, has been identified and associated with cancer and various other diseases. Ferroptosis is defined as a reactive oxygen species (ROS)-dependent cell death related to iron accumulation and lipid peroxidation, which is different from apoptosis, necrosis, autophagy, and other forms of cell death. However, accumulating evidence has revealed a link between autophagy and ferroptosis at the molecular level and has suggested that autophagy is involved in regulating the accumulation of iron-dependent lipid peroxidation and ROS during ferroptosis. Understanding the roles and pathophysiological processes of autophagy during ferroptosis may provide effective strategies for the treatment of ferroptosis-related diseases. In this review, we summarize the current knowledge regarding the regulatory mechanisms underlying ferroptosis, including iron and lipid metabolism, and its association with the autophagy pathway. In addition, we discuss the contribution of autophagy to ferroptosis and elucidate the role of autophagy as a ferroptosis enhancer during ROS-dependent ferroptosis.
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