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Ferroptosis: A potential therapeutic target in autoimmune disease (Review)
Ferroptosis is a distinct type of regulated cell death characterized by iron overload and lipid peroxidation. Ferroptosis is regulated by numerous factors and controlled by several mechanisms. This cell death type has a relationship with the immune system, which may be regulated by damage-associated...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
D.A. Spandidos
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10318600/ https://www.ncbi.nlm.nih.gov/pubmed/37408857 http://dx.doi.org/10.3892/etm.2023.12067 |
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author | Shen, Liang Wang, Xiaohan Zhai, Changlin Chen, Yunqing |
author_facet | Shen, Liang Wang, Xiaohan Zhai, Changlin Chen, Yunqing |
author_sort | Shen, Liang |
collection | PubMed |
description | Ferroptosis is a distinct type of regulated cell death characterized by iron overload and lipid peroxidation. Ferroptosis is regulated by numerous factors and controlled by several mechanisms. This cell death type has a relationship with the immune system, which may be regulated by damage-associated molecular patterns. Ferroptosis participates in the progression of autoimmune diseases, including autoimmune hepatitis, rheumatoid arthritis, systemic lupus erythematosus, inflammatory bowel disease, multiple sclerosis, Parkinson's Disease, psoriasis and insulin-dependent diabetes mellitus. The present review summarizes the role of ferroptosis in autoimmune disorders and discusses ferroptosis as a potential therapeutic target for autoimmune disease. |
format | Online Article Text |
id | pubmed-10318600 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | D.A. Spandidos |
record_format | MEDLINE/PubMed |
spelling | pubmed-103186002023-07-05 Ferroptosis: A potential therapeutic target in autoimmune disease (Review) Shen, Liang Wang, Xiaohan Zhai, Changlin Chen, Yunqing Exp Ther Med Review Ferroptosis is a distinct type of regulated cell death characterized by iron overload and lipid peroxidation. Ferroptosis is regulated by numerous factors and controlled by several mechanisms. This cell death type has a relationship with the immune system, which may be regulated by damage-associated molecular patterns. Ferroptosis participates in the progression of autoimmune diseases, including autoimmune hepatitis, rheumatoid arthritis, systemic lupus erythematosus, inflammatory bowel disease, multiple sclerosis, Parkinson's Disease, psoriasis and insulin-dependent diabetes mellitus. The present review summarizes the role of ferroptosis in autoimmune disorders and discusses ferroptosis as a potential therapeutic target for autoimmune disease. D.A. Spandidos 2023-06-15 /pmc/articles/PMC10318600/ /pubmed/37408857 http://dx.doi.org/10.3892/etm.2023.12067 Text en Copyright: © Shen et al. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made. |
spellingShingle | Review Shen, Liang Wang, Xiaohan Zhai, Changlin Chen, Yunqing Ferroptosis: A potential therapeutic target in autoimmune disease (Review) |
title | Ferroptosis: A potential therapeutic target in autoimmune disease (Review) |
title_full | Ferroptosis: A potential therapeutic target in autoimmune disease (Review) |
title_fullStr | Ferroptosis: A potential therapeutic target in autoimmune disease (Review) |
title_full_unstemmed | Ferroptosis: A potential therapeutic target in autoimmune disease (Review) |
title_short | Ferroptosis: A potential therapeutic target in autoimmune disease (Review) |
title_sort | ferroptosis: a potential therapeutic target in autoimmune disease (review) |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10318600/ https://www.ncbi.nlm.nih.gov/pubmed/37408857 http://dx.doi.org/10.3892/etm.2023.12067 |
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