Ferroptosis at the crossroads of cancer-acquired drug resistance and immune evasion

被引:1200
作者
Angeli, Jose Pedro Friedmann [1 ]
Krysko, Dmitri, V [2 ,3 ,4 ]
Conrad, Marcus [5 ]
机构
[1] Univ Wurzburg, Rudolf Virchow Ctr Expt Biomed, Wurzburg, Germany
[2] Univ Ghent, Dept Human Struct & Repair, Ghent, Belgium
[3] CRIG, Ghent, Belgium
[4] Natl Res Lobachevsky State Univ Nizhny Novgorod, Inst Biol & Biomed, Nizhnii Novgorod, Russia
[5] Helmholtz Zentrum Munchen, Inst Dev Genet, Neuherberg, Germany
关键词
HYDROPEROXIDE GLUTATHIONE-PEROXIDASE; CELL-DEATH; APOPTOTIC CELLS; ARACHIDONATE METABOLISM; INHIBITS FERROPTOSIS; LIPID-PEROXIDATION; TARGETED THERAPY; DENDRITIC CELLS; BREAST-CANCER; REDOX STATE;
D O I
10.1038/s41568-019-0149-1
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Ferroptosis is a recently recognized cell death modality that is morphologically, biochemically and genetically distinct from other forms of cell death and that has emerged to play an important role in cancer biology. Recent discoveries have highlighted the metabolic plasticity of cancer cells and have provided intriguing insights into how metabolic rewiring is a critical event for the persistence, dedifferentiation and expansion of cancer cells. In some cases, this metabolic reprogramming has been linked to an acquired sensitivity to ferroptosis, thus opening up new opportunities to treat therapy-insensitive tumours. However, it is not yet clear what metabolic determinants are critical for therapeutic resistance and evasion of immune surveillance. Therefore, a better understanding of the processes that regulate ferroptosis sensitivity should ultimately aid in the discovery of novel therapeutic strategies to improve cancer treatment. In this Perspectives article, we provide an overview of the known mechanisms that regulate sensitivity to ferroptosis in cancer cells and how the modulation of metabolic pathways controlling ferroptosis might reshape the tumour niche, leading to an immunosuppressive microenvironment that promotes tumour growth and progression.
引用
收藏
页码:405 / 414
页数:10
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