Targeting ferroptosis as a vulnerability in cancer

被引:1591
作者
Lei, Guang [1 ]
Zhuang, Li [1 ]
Gan, Boyi [1 ,2 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Expt Radiat Oncol, Houston, TX 77030 USA
[2] Univ Texas MD Anderson UTHlth Grad Sch Biomed Sci, Houston, TX 77030 USA
基金
美国国家卫生研究院;
关键词
HYDROPEROXIDE GLUTATHIONE-PEROXIDASE; CELL-DEATH; TUMOR-SUPPRESSOR; LIPID-PEROXIDATION; PROMOTES FERROPTOSIS; SYNTHETIC LETHALITY; TRANSPORT ACTIVITY; NUCLEAR FORM; METABOLISM; PATHWAY;
D O I
10.1038/s41568-022-00459-0
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Ferroptosis is an iron-dependent form of regulated cell death that is triggered by the toxic build-up of lipid peroxides on cellular membranes. In recent years, ferroptosis has garnered enormous interest in cancer research communities, partly because it is a unique cell death modality that is mechanistically and morphologically different from other forms of cell death, such as apoptosis, and therefore holds great potential for cancer therapy. In this Review, we summarize the current understanding of ferroptosis-inducing and ferroptosis defence mechanisms, dissect the roles and mechanisms of ferroptosis in tumour suppression and tumour immunity, conceptualize the diverse vulnerabilities of cancer cells to ferroptosis, and explore therapeutic strategies for targeting ferroptosis in cancer. In recent years, research in the field of ferroptosis in cancer has risen steeply in part owing to its potential to be targeted. In this Review, Lei et al. provide an up-to-date synthesis of the roles and mechanisms of ferroptosis in tumour growth and progression, including its function in tumour immunity, highlighting it as a vulnerability that can be exploited for cancer therapy.
引用
收藏
页码:381 / 396
页数:16
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