程序性细胞死亡
串扰
炎症
癌症
癌细胞
GPX4
生物
癌症研究
功能(生物学)
细胞凋亡
细胞生物学
免疫学
氧化应激
遗传学
生物化学
光学
物理
谷胱甘肽过氧化物酶
过氧化氢酶
作者
Xin Jin,Jiao Tang,Xiangyu Qiu,X. Nie,S.-H.I. Ou,Geyan Wu,Rongxin Zhang,Jinrong Zhu
标识
DOI:10.1038/s41420-024-01825-7
摘要
Abstract Ferroptosis represents a distinct form of programmed cell death triggered by excessive iron accumulation and lipid peroxidation-induced damage. This mode of cell death differentiates from classical programmed cell death in terms of morphology and biochemistry. Ferroptosis stands out for its exceptional biological characteristics and has garnered extensive research and conversations as a form of programmed cell death. Its dysfunctional activation is closely linked to the onset of diseases, particularly inflammation and cancer, making ferroptosis a promising avenue for combating these conditions. As such, exploring ferroptosis may offer innovative approaches to treating cancer and inflammatory diseases. Our review provides insights into the relevant regulatory mechanisms of ferroptosis, examining the impact of ferroptosis-related factors from both physiological and pathological perspectives. Describing the crosstalk between ferroptosis and tumor- and inflammation-associated signaling pathways and the potential of ferroptosis inducers in overcoming drug-resistant cancers are discussed, aiming to inform further novel therapeutic directions for ferroptosis in relation to inflammatory and cancer diseases.
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