Cashing in on ferroptosis against tumor cells: Usher in the next chapter.
Cancer therapy
Chemoresistance
Ferroptosis
Oxidative stress
Tumor immunity
Journal
Life sciences
ISSN: 1879-0631
Titre abrégé: Life Sci
Pays: Netherlands
ID NLM: 0375521
Informations de publication
Date de publication:
15 Nov 2021
15 Nov 2021
Historique:
received:
08
06
2021
revised:
30
08
2021
accepted:
10
09
2021
pubmed:
18
9
2021
medline:
16
11
2021
entrez:
17
9
2021
Statut:
ppublish
Résumé
Ferroptosis is a new type of non-apoptotic regulated cell death (RCD) driven by unrestricted lethal lipid peroxidation, which is totally distinct from other forms of RCD in genetic and biochemical characteristics. It is generally believed that iron dependency, malfunction of the redox system, and excessive lipid peroxidation are the main hallmarks of ferroptosis. Accumulating pieces of evidence over the past few years have shown that ferroptosis is tightly related to various types of diseases, especially cancers. Ferroptosis has recently attracted great attention in the field of cancer research. A plethora of evidence shows that employing ferroptosis as a powerful weapon can remarkably enhance the efficacy of tumor cell annihilation. Better knowledge of the ferroptosis mechanisms and their interplay with cancer biology would enable us to use this fashionable tool in the best way. Herein, we will briefly present the relevant mechanisms of ferroptosis, the multifaceted relation between ferroptosis and cancer, encompassing tumor immunity, overcoming chemoresistance, and epithelial to mesenchymal transition. In the end, we will also briefly discuss the potential approaches to ferroptosis-based cancer therapy, such as using drugs and small molecules, nanoparticles, mitochondrial targeting, and photodynamic therapy.
Identifiants
pubmed: 34534562
pii: S0024-3205(21)00945-0
doi: 10.1016/j.lfs.2021.119958
pii:
doi:
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
119958Informations de copyright
Copyright © 2021. Published by Elsevier Inc.