Targeting Ferroptosis to Iron Out Cancer

被引:1870
|
作者
Hassannia, Behrouz [1 ,2 ]
Vandenabeele, Peter [1 ,2 ,3 ]
Vanden Berghe, Tom [1 ,2 ,4 ,5 ,6 ]
机构
[1] VIB Ctr Inflammat Res IRC, Ghent, Belgium
[2] Univ Ghent, DBMB, Ghent, Belgium
[3] Univ Ghent, Methusalem Program, Ghent, Belgium
[4] Univ Antwerp, Dept Biomed Sci, Lab Pathophysiol, B-2000 Antwerp, Belgium
[5] VIB Ghent Univ, FAIR, Antwerp, Belgium
[6] Univ Antwerp, Antwerp, Belgium
关键词
DEPENDENT CELL-DEATH; BUTHIONINE SULFOXIMINE; TUMOR-SUPPRESSOR; INHIBITS FERROPTOSIS; GLUTAMATE TOXICITY; THERAPEUTIC TARGET; LIPID-PEROXIDATION; OXIDATIVE STRESS; CYCLE ARREST; GLUTATHIONE;
D O I
10.1016/j.ccell.2019.04.002
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
One of the key challenges in cancer research how to effectively kill cancer cells while leaving the healthy cells intact. Cancer cells often have defects in cell death executioner mechanisms, which is one of the r. An reasons for therapy resistance. To enable growth, cancer cells exhibit an increased iron demand compared with normal, non-cancer cells. This iron dependency can make cancer cells more vulnerable to iron-catalyzed necrosis, referred to as ferroptosis. The identification of FDA-approved drugs as ferroptosis inducers creates high expectations for the potential of ferroptosis to be a new promising way to kill therapy-resistant cancers.
引用
收藏
页码:830 / 849
页数:20
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