Reprogramming the chemical reactivity of iron in cancer stem cells

被引:2
|
作者
Caneque, Tatiana [1 ,2 ,3 ,4 ]
Mueller, Sebastian [1 ,2 ,3 ,4 ]
Lafon, Anne [1 ,2 ,3 ,4 ]
Sindikubwabo, Fabien [1 ,2 ,3 ,4 ]
Versini, Antoine [1 ,2 ,3 ,4 ]
Saier, Lou [1 ,2 ,3 ,4 ]
Barutaut, Manon [1 ,2 ,3 ,4 ]
Gaillet, Christine [1 ,2 ,3 ,4 ]
Rodriguez, Raphael [1 ,2 ,3 ,4 ]
机构
[1] Inst Curie, 26 Rue Ulm, F-75005 Paris, France
[2] PSL Res Univ, Paris, France
[3] CNRS, UMR 3666, Paris, France
[4] INSERM, U1143, Chem Biol Canc Team, Equipe Labellisee Ligue Natl Canc, Paris, France
基金
欧洲研究理事会;
关键词
Cancer; Cancer stem cells; Salinomycin; Lysosome; Iron; Fenton reaction; Ferroptosis; SALINOMYCIN; INHIBITION;
D O I
10.1016/j.crci.2018.03.012
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Cancer stem cells (CSCs) have been shown to be refractory to conventional therapeutic agents, can promote metastasis, and have been linked to cancer relapse. Salinomycin can selectively kill CSCs. We have shown that salinomycin derivatives accumulate in lysosomes and sequester iron in this organelle. As a result, accumulation of iron leads to the production of reactive oxygen species and lysosomal membrane permeabilization, which in turn promotes cell death by ferroptosis. These findings have revealed the prevalence of iron homeostasis in CSCs and paved the way toward the development of next-generation therapeutics. (C) 2018 Academie des sciences. Published by Elsevier Masson SAS.
引用
收藏
页码:704 / 708
页数:5
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