GPX4
坏死性下垂
裂谷1
癌细胞
程序性细胞死亡
癌症
癌症研究
细胞凋亡
生物
细胞生物学
氧化应激
谷胱甘肽过氧化物酶
生物化学
遗传学
过氧化氢酶
作者
Christina M. Bebber,Fabienne Müller,Laura Prieto Clemente,Josephine Weber,Silvia von Karstedt
出处
期刊:Cancers
[MDPI AG]
日期:2020-01-09
卷期号:12 (1): 164-164
被引量:233
标识
DOI:10.3390/cancers12010164
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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