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System X(c) (−)/GSH/GPX4 axis: An important antioxidant system for the ferroptosis in drug-resistant solid tumor therapy
The activation of ferroptosis is a new effective way to treat drug-resistant solid tumors. Ferroptosis is an iron-mediated form of cell death caused by the accumulation of lipid peroxides. The intracellular imbalance between oxidant and antioxidant due to the abnormal expression of multiple redox ac...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9465090/ https://www.ncbi.nlm.nih.gov/pubmed/36105219 http://dx.doi.org/10.3389/fphar.2022.910292 |
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author | Li, Feng-Jiao Long, Hui-Zhi Zhou, Zi-Wei Luo, Hong-Yu Xu, Shuo-Guo Gao, Li-Chen |
author_facet | Li, Feng-Jiao Long, Hui-Zhi Zhou, Zi-Wei Luo, Hong-Yu Xu, Shuo-Guo Gao, Li-Chen |
author_sort | Li, Feng-Jiao |
collection | PubMed |
description | The activation of ferroptosis is a new effective way to treat drug-resistant solid tumors. Ferroptosis is an iron-mediated form of cell death caused by the accumulation of lipid peroxides. The intracellular imbalance between oxidant and antioxidant due to the abnormal expression of multiple redox active enzymes will promote the produce of reactive oxygen species (ROS). So far, a few pathways and regulators have been discovered to regulate ferroptosis. In particular, the cystine/glutamate antiporter (System X(c) (−)), glutathione peroxidase 4 (GPX4) and glutathione (GSH) (System X(c) (−)/GSH/GPX4 axis) plays a key role in preventing lipid peroxidation-mediated ferroptosis, because of which could be inhibited by blocking System X(c) (−)/GSH/GPX4 axis. This review aims to present the current understanding of the mechanism of ferroptosis based on the System X(c) (−)/GSH/GPX4 axis in the treatment of drug-resistant solid tumors. |
format | Online Article Text |
id | pubmed-9465090 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-94650902022-09-13 System X(c) (−)/GSH/GPX4 axis: An important antioxidant system for the ferroptosis in drug-resistant solid tumor therapy Li, Feng-Jiao Long, Hui-Zhi Zhou, Zi-Wei Luo, Hong-Yu Xu, Shuo-Guo Gao, Li-Chen Front Pharmacol Pharmacology The activation of ferroptosis is a new effective way to treat drug-resistant solid tumors. Ferroptosis is an iron-mediated form of cell death caused by the accumulation of lipid peroxides. The intracellular imbalance between oxidant and antioxidant due to the abnormal expression of multiple redox active enzymes will promote the produce of reactive oxygen species (ROS). So far, a few pathways and regulators have been discovered to regulate ferroptosis. In particular, the cystine/glutamate antiporter (System X(c) (−)), glutathione peroxidase 4 (GPX4) and glutathione (GSH) (System X(c) (−)/GSH/GPX4 axis) plays a key role in preventing lipid peroxidation-mediated ferroptosis, because of which could be inhibited by blocking System X(c) (−)/GSH/GPX4 axis. This review aims to present the current understanding of the mechanism of ferroptosis based on the System X(c) (−)/GSH/GPX4 axis in the treatment of drug-resistant solid tumors. Frontiers Media S.A. 2022-08-29 /pmc/articles/PMC9465090/ /pubmed/36105219 http://dx.doi.org/10.3389/fphar.2022.910292 Text en Copyright © 2022 Li, Long, Zhou, Luo, Xu and Gao. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Pharmacology Li, Feng-Jiao Long, Hui-Zhi Zhou, Zi-Wei Luo, Hong-Yu Xu, Shuo-Guo Gao, Li-Chen System X(c) (−)/GSH/GPX4 axis: An important antioxidant system for the ferroptosis in drug-resistant solid tumor therapy |
title | System X(c)
(−)/GSH/GPX4 axis: An important antioxidant system for the ferroptosis in drug-resistant solid tumor therapy |
title_full | System X(c)
(−)/GSH/GPX4 axis: An important antioxidant system for the ferroptosis in drug-resistant solid tumor therapy |
title_fullStr | System X(c)
(−)/GSH/GPX4 axis: An important antioxidant system for the ferroptosis in drug-resistant solid tumor therapy |
title_full_unstemmed | System X(c)
(−)/GSH/GPX4 axis: An important antioxidant system for the ferroptosis in drug-resistant solid tumor therapy |
title_short | System X(c)
(−)/GSH/GPX4 axis: An important antioxidant system for the ferroptosis in drug-resistant solid tumor therapy |
title_sort | system x(c)
(−)/gsh/gpx4 axis: an important antioxidant system for the ferroptosis in drug-resistant solid tumor therapy |
topic | Pharmacology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9465090/ https://www.ncbi.nlm.nih.gov/pubmed/36105219 http://dx.doi.org/10.3389/fphar.2022.910292 |
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