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GPX4-independent ferroptosis—a new strategy in disease’s therapy
Ferroptosis is a form of programmed cell death characterized by intracellular iron accumulation and lipid peroxidation, and earlier studies identified glutathione peroxidase 4 (GPX4) as an essential regulator of this process. Ferroptosis plays an essential role in tumors, degenerative diseases, and...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9617873/ https://www.ncbi.nlm.nih.gov/pubmed/36309489 http://dx.doi.org/10.1038/s41420-022-01212-0 |
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author | Ma, Tianyu Du, Jingtong Zhang, Yufeng Wang, Yuyao Wang, Bingxuan Zhang, Tianhong |
author_facet | Ma, Tianyu Du, Jingtong Zhang, Yufeng Wang, Yuyao Wang, Bingxuan Zhang, Tianhong |
author_sort | Ma, Tianyu |
collection | PubMed |
description | Ferroptosis is a form of programmed cell death characterized by intracellular iron accumulation and lipid peroxidation, and earlier studies identified glutathione peroxidase 4 (GPX4) as an essential regulator of this process. Ferroptosis plays an essential role in tumors, degenerative diseases, and ischemia-reperfusion injury. However, researchers have found that inhibition of GPX4 does not entirely suppress ferroptosis in certain diseases, or cells express resistance to ferroptosis agonists that inhibit GPX4. As research progresses, it has been discovered that there are multiple regulatory pathways for ferroptosis that are independent of GPX4. The study of GPX4-independent ferroptosis pathways can better target ferroptosis to prevent and treat various diseases. Here, the currently inhibited pulmonary GPX4-dependent ferroptosis pathways will be reviewed. |
format | Online Article Text |
id | pubmed-9617873 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-96178732022-10-31 GPX4-independent ferroptosis—a new strategy in disease’s therapy Ma, Tianyu Du, Jingtong Zhang, Yufeng Wang, Yuyao Wang, Bingxuan Zhang, Tianhong Cell Death Discov Review Article Ferroptosis is a form of programmed cell death characterized by intracellular iron accumulation and lipid peroxidation, and earlier studies identified glutathione peroxidase 4 (GPX4) as an essential regulator of this process. Ferroptosis plays an essential role in tumors, degenerative diseases, and ischemia-reperfusion injury. However, researchers have found that inhibition of GPX4 does not entirely suppress ferroptosis in certain diseases, or cells express resistance to ferroptosis agonists that inhibit GPX4. As research progresses, it has been discovered that there are multiple regulatory pathways for ferroptosis that are independent of GPX4. The study of GPX4-independent ferroptosis pathways can better target ferroptosis to prevent and treat various diseases. Here, the currently inhibited pulmonary GPX4-dependent ferroptosis pathways will be reviewed. Nature Publishing Group UK 2022-10-30 /pmc/articles/PMC9617873/ /pubmed/36309489 http://dx.doi.org/10.1038/s41420-022-01212-0 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Review Article Ma, Tianyu Du, Jingtong Zhang, Yufeng Wang, Yuyao Wang, Bingxuan Zhang, Tianhong GPX4-independent ferroptosis—a new strategy in disease’s therapy |
title | GPX4-independent ferroptosis—a new strategy in disease’s therapy |
title_full | GPX4-independent ferroptosis—a new strategy in disease’s therapy |
title_fullStr | GPX4-independent ferroptosis—a new strategy in disease’s therapy |
title_full_unstemmed | GPX4-independent ferroptosis—a new strategy in disease’s therapy |
title_short | GPX4-independent ferroptosis—a new strategy in disease’s therapy |
title_sort | gpx4-independent ferroptosis—a new strategy in disease’s therapy |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9617873/ https://www.ncbi.nlm.nih.gov/pubmed/36309489 http://dx.doi.org/10.1038/s41420-022-01212-0 |
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