Revisiting Tumors and the Cardiovascular System: Mechanistic Intersections and Divergences in Ferroptosis.
Journal
Oxidative medicine and cellular longevity
ISSN: 1942-0994
Titre abrégé: Oxid Med Cell Longev
Pays: United States
ID NLM: 101479826
Informations de publication
Date de publication:
2020
2020
Historique:
received:
03
06
2020
revised:
10
07
2020
accepted:
20
07
2020
entrez:
10
9
2020
pubmed:
11
9
2020
medline:
13
5
2021
Statut:
epublish
Résumé
Ferroptosis was recently identified as an iron-dependent regulatory necrosis process mediated by polyunsaturated fatty acid (PUFA) peroxidation. The pivotal events related to oxidative stress in ferroptosis include direct or indirect glutathione peroxidase 4 (GPX4) inhibition, ferrous iron overload, and lipid peroxidation. The links between ferroptosis and multiple pathological processes including tumor and cardiovascular system disease have become increasingly apparent, and the mechanisms and compounds involved in ferroptosis, such as reduction of coenzyme Q
Identifiants
pubmed: 32908642
doi: 10.1155/2020/9738143
pmc: PMC7450308
doi:
Substances chimiques
Endoplasmic Reticulum Chaperone BiP
0
HSPA5 protein, human
0
Reactive Oxygen Species
0
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
9738143Informations de copyright
Copyright © 2020 Yani Wang et al.
Déclaration de conflit d'intérêts
The authors declare that they have no conflict of interest.
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