Ferroptosis in cardiovascular diseases : role and mechanism

© 2023. The Author(s)..

In multicellular organisms, regulatory cell death is a crucial aspect of growth and development. Ferroptosis, which was postulated roughly ten years ago, is a mode of cell death that differs from apoptosis, autophagy, and pyrodeath. This distinct pattern of cell death is triggered by an imbalance between oxidants and antioxidants and strongly associated with the metabolism of iron, lipids, amino acids, and glutathione. A growing body of research has implicated ferroptosis in the incidence and progression of many organ traumas and degenerative diseases. Recently, ferroptosis has gained attention as a crucial regulatory mechanism underlying the initiation and development of a variety of cardiovascular diseases, including myocardial ischemia/reperfusion injury, cardiomyopathy, arrhythmia, chemotherapy, and Corona Virus-2-induced cardiac injury. Pharmacological therapies that inhibit ferroptosis have great potential for the management of cardiovascular disorders. This review discusses the prevalence and regulatory mechanisms of ferroptosis, effect of ferroptosis on the immune system, significance of ferroptosis in cardiovascular diseases, and potential therapeutic value of regulating ferroptosis in a variety of heart diseases.

Medienart:

E-Artikel

Erscheinungsjahr:

2023

Erschienen:

2023

Enthalten in:

Zur Gesamtaufnahme - volume:13

Enthalten in:

Cell & bioscience - 13(2023), 1 vom: 15. Dez., Seite 226

Sprache:

Englisch

Beteiligte Personen:

Zhang, Qi [VerfasserIn]
Luo, Yuhao [VerfasserIn]
Peng, Lin [VerfasserIn]
Rong, Xi [VerfasserIn]
Liu, Yingxue [VerfasserIn]
Li, Jiafu [VerfasserIn]
Luo, Jing [VerfasserIn]

Links:

Volltext

Themen:

Cardiovascular disease
Corona Virus-2
Ferroptosis
Journal Article
Regulated cell death
Review

Anmerkungen:

Date Revised 18.12.2023

published: Electronic

Citation Status PubMed-not-MEDLINE

doi:

10.1186/s13578-023-01169-2

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

NLM365933562