Ferroptosis in hepatocellular carcinoma: mechanisms and targeted therapy

被引:91
作者
Ajoolabady, Amir [1 ]
Tang, Daolin [2 ]
Kroemer, Guido [3 ,4 ,5 ]
Ren, Jun [1 ]
机构
[1] Fudan Univ, Shanghai Inst Cardiovasc Dis, Dept Cardiol, Zhongshan Hosp, Shanghai, Peoples R China
[2] UT Southwestern Med Ctr, Dept Surg, Dallas, TX 75390 USA
[3] Sorbonne Univ, Equipe Labellisee Ligue Canc, Inst Univ France, Ctr Rech Cordeliers,Univ Paris,Inserm U1138, Paris, France
[4] Inst Gustave Roussy, Metabol & Cell Biol Platforms, Villejuif, France
[5] Hop Europeen Georges Pompidou, AP HP, Pole Biol, Paris, France
基金
欧盟地平线“2020”;
关键词
CELL-DEATH; NONALCOHOLIC STEATOHEPATITIS; PROMOTES FERROPTOSIS; LIPID-PEROXIDATION; IRON; CANCER; METABOLISM; RESISTANCE; PROTEIN; IDENTIFICATION;
D O I
10.1038/s41416-022-01998-x
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Hepatocellular carcinoma is the most prevalent form of primary liver cancer with a multifactorial aetiology comprising genetic, environmental, and behavioural factors. Evading cell death is a defining hallmark of hepatocellular carcinoma, underpinning tumour growth, progression, and therapy resistance. Ferroptosis is a form of nonapoptotic cell death driven by an array of cellular events, including intracellular iron overload, free radical production, lipid peroxidation and activation of various cell death effectors, ultimately leading to rupture of the plasma membrane. Although induction of ferroptosis is an emerging strategy to suppress hepatocellular carcinoma, malignant cells manage to develop adaptive mechanisms, conferring resistance to ferroptosis and ferroptosis-inducing drugs. Herein, we aim at elucidating molecular mechanisms and signalling pathways involved in ferroptosis and offer our opinions on druggable targets and new therapeutic strategy in an attempt to restrain the growth and progression of hepatocellular carcinoma through induction of ferroptotic cell death.
引用
收藏
页码:190 / 205
页数:16
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