Ferroptosis in Cancer Cell Biology

被引:303
作者
Bebber, Christina M. [1 ,2 ,3 ]
Mueller, Fabienne [1 ,2 ]
Clemente, Laura Prieto [1 ,2 ]
Weber, Josephine [1 ,2 ]
von Karstedt, Silvia [1 ,2 ]
机构
[1] Univ Cologne, Fac Med, Dept Translat Genom, Weyertal 155b, D-50931 Cologne, Germany
[2] Univ Cologne, Cologne Excellence Cluster Cellular Stress Respon, Fac Med, Joseph Stelzmann Str 26, D-50931 Cologne, Germany
[3] Univ Hosp Cologne, Dept Internal Med 1, Kerpener Str 62, D-50937 Cologne, Germany
关键词
ferroptosis; cancer; cell death; GPX4; inflammation; GLUTATHIONE-PEROXIDASE; 4; TUMOR-ASSOCIATED MACROPHAGES; CYSTATHIONINE BETA-SYNTHASE; OXIDATIVE STRESS; CYSTINE/GLUTAMATE ANTIPORTER; DEATH RECOMMENDATIONS; TRANSCRIPTION FACTOR; LIPID-PEROXIDATION; MOUSE DEVELOPMENT; GENE-EXPRESSION;
D O I
10.3390/cancers12010164
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
A major hallmark of cancer is successful evasion of regulated forms of cell death. Ferroptosis is a recently discovered type of regulated necrosis which, unlike apoptosis or necroptosis, is independent of caspase activity and receptor-interacting protein 1 (RIPK1) kinase activity. Instead, ferroptotic cells die following iron-dependent lipid peroxidation, a process which is antagonised by glutathione peroxidase 4 (GPX4) and ferroptosis suppressor protein 1 (FSP1). Importantly, tumour cells escaping other forms of cell death have been suggested to maintain or acquire sensitivity to ferroptosis. Therefore, therapeutic exploitation of ferroptosis in cancer has received increasing attention. Here, we systematically review current literature on ferroptosis signalling, cross-signalling to cellular metabolism in cancer and a potential role for ferroptosis in tumour suppression and tumour immunology. By summarising current findings on cell biology relevant to ferroptosis in cancer, we aim to point out new conceptual avenues for utilising ferroptosis in systemic treatment approaches for cancer.
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页数:24
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