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Persister cancer cells: Iron addiction and vulnerability to ferroptosis.
Rodriguez, Raphaël; Schreiber, Stuart L; Conrad, Marcus.
Afiliação
  • Rodriguez R; Chemical Biology of Cancer at Institut Curie, PSL Research University, CNRS UMR 3666, INSERM U1143, Paris, France. Electronic address: raphael.rodriguez@curie.fr.
  • Schreiber SL; Chemical Biology and Therapeutics Science Program, Broad Institute, Cambridge, MA 02142, USA; Department of Chemistry and Chemical Biology, Harvard University, Cambridge, MA 02138, USA. Electronic address: stuart_schreiber@harvard.edu.
  • Conrad M; Institute of Metabolism and Cell Death, Helmholtz Zentrum München, 85764 Neuherberg, Germany; Pirogov National Research Medical University, Laboratory of Experimental Oncology, Moscow 117997, Russia. Electronic address: marcus.conrad@helmholtz-muenchen.de.
Mol Cell ; 82(4): 728-740, 2022 02 17.
Article em En | MEDLINE | ID: mdl-34965379
ABSTRACT
Ferroptosis is a unique type of non-apoptotic cell death resulting from the unrestrained occurrence of peroxidized phospholipids, which are subject to iron-mediated production of lethal oxygen radicals. This cell death modality has been detected across many organisms, including in mammals, where it can be used as a defense mechanism against pathogens or even harnessed by T cells to sensitize tumor cells toward effective killing. Conversely, ferroptosis is considered one of the main cell death mechanisms promoting degenerative diseases. Emerging evidence suggests that ferroptosis represents a vulnerability in certain cancers. Here, we critically review recent advances linking ferroptosis vulnerabilities of dedifferentiating and persister cancer cells to the dependency of these cells on iron, a potential Achilles heel for small-molecule intervention. We provide a perspective on the mechanisms reliant on iron that contribute to the persister cancer cell state and how this dependency may be exploited for therapeutic benefits.
Assuntos

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Células-Tronco Neoplásicas / Peroxidação de Lipídeos / Espécies Reativas de Oxigênio / Ferroptose / Ferro / Neoplasias Limite: Animals / Humans Idioma: En Revista: Mol Cell Assunto da revista: BIOLOGIA MOLECULAR Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Células-Tronco Neoplásicas / Peroxidação de Lipídeos / Espécies Reativas de Oxigênio / Ferroptose / Ferro / Neoplasias Limite: Animals / Humans Idioma: En Revista: Mol Cell Assunto da revista: BIOLOGIA MOLECULAR Ano de publicação: 2022 Tipo de documento: Article