Selenium: Tracing Another Essential Element of Ferroptotic Cell Death.


Journal

Cell chemical biology
ISSN: 2451-9448
Titre abrégé: Cell Chem Biol
Pays: United States
ID NLM: 101676030

Informations de publication

Date de publication:
16 04 2020
Historique:
received: 08 01 2020
revised: 02 03 2020
accepted: 17 03 2020
pubmed: 11 4 2020
medline: 13 5 2021
entrez: 11 4 2020
Statut: ppublish

Résumé

The trace elements iron and selenium play decisive roles in a distinct form of necrotic cell death, known as ferroptosis. While iron promotes ferroptosis by contributing to Fenton-type reactions and uncontrolled lipid autoxidation, the hallmark of ferroptosis, selenium in the form of glutathione peroxidase 4 (GPX4), subdues phospholipid peroxidation and associated cell death. Beyond the canonical cystine/glutamate antiporter system x

Identifiants

pubmed: 32275866
pii: S2451-9456(20)30109-4
doi: 10.1016/j.chembiol.2020.03.012
pii:
doi:

Substances chimiques

S100 Calcium-Binding Protein A4 0
Selenoproteins 0
Sulfhydryl Compounds 0
Iron E1UOL152H7
Phospholipid Hydroperoxide Glutathione Peroxidase EC 1.11.1.12
Selenium H6241UJ22B

Types de publication

Journal Article Research Support, Non-U.S. Gov't Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

409-419

Informations de copyright

Copyright © 2020 Elsevier Ltd. All rights reserved.

Auteurs

Marcus Conrad (M)

Institute of Metabolism and Cell Death, Helmholtz Zentrum München, 85764 Neuherberg, Germany; National Research Medical University, Laboratory of Experimental Oncology, Ostrovityanova 1, Moscow 117997, Russia. Electronic address: marcus.conrad@helmholtz-muenchen.de.

Bettina Proneth (B)

Institute of Metabolism and Cell Death, Helmholtz Zentrum München, 85764 Neuherberg, Germany.

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Classifications MeSH