A Smooth Muscle Cell-Based Ferroptosis Model to Evaluate Iron-Chelating Molecules for Cardiovascular Disease Treatment.
ferroptosis
human aortic smooth muscle cells
intracellular GSH
iron chelation
lipid peroxidation
Journal
Current issues in molecular biology
ISSN: 1467-3045
Titre abrégé: Curr Issues Mol Biol
Pays: Switzerland
ID NLM: 100931761
Informations de publication
Date de publication:
04 Feb 2024
04 Feb 2024
Historique:
received:
21
11
2023
revised:
24
01
2024
accepted:
29
01
2024
medline:
23
2
2024
pubmed:
23
2
2024
entrez:
23
2
2024
Statut:
epublish
Résumé
Dysregulation of iron homeostasis causes iron-mediated cell death, recently described as ferroptosis. Ferroptosis is reported in many chronic diseases, such as hepatic cancer, renal, and cardiovascular diseases (heart failure, atherosclerosis). However, there is a notable scarcity of research studies in the existing literature that explore treatments capable of preventing ferroptosis. Additionally, as far as the author is aware, there is currently no established model for studying ferroptosis within cardiovascular cells, which would be essential for assessing metal-chelating molecules with the potential ability to inhibit ferroptosis and their application in the treatment of cardiovascular diseases. In this study, a smooth muscle cell-based ferroptosis model is developed upon the inhibition of the system X
Identifiants
pubmed: 38392204
pii: cimb46020086
doi: 10.3390/cimb46020086
doi:
Types de publication
Journal Article
Langues
eng
Pagination
1348-1359Subventions
Organisme : Agence Nationale de la Recherche
ID : 15-004
Organisme : Agence Nationale de la Recherche
ID : JCJC MELISSA (2020)