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Insights on Ferroptosis and Colorectal Cancer: Progress and Updates
Patients with advanced-stage or treatment-resistant colorectal cancer (CRC) benefit less from traditional therapies; hence, new therapeutic strategies may help improve the treatment response and prognosis of these patients. Ferroptosis is an iron-dependent type of regulated cell death characterized...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9821926/ https://www.ncbi.nlm.nih.gov/pubmed/36615434 http://dx.doi.org/10.3390/molecules28010243 |
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author | Hu, Bangli Yin, Yixin Li, Siqi Guo, Xianwen |
author_facet | Hu, Bangli Yin, Yixin Li, Siqi Guo, Xianwen |
author_sort | Hu, Bangli |
collection | PubMed |
description | Patients with advanced-stage or treatment-resistant colorectal cancer (CRC) benefit less from traditional therapies; hence, new therapeutic strategies may help improve the treatment response and prognosis of these patients. Ferroptosis is an iron-dependent type of regulated cell death characterized by the accumulation of lipid reactive oxygen species (ROS), distinct from other types of regulated cell death. CRC cells, especially those with drug-resistant properties, are characterized by high iron levels and ROS. This indicates that the induction of ferroptosis in these cells may become a new therapeutic approach for CRC, particularly for eradicating CRC resistant to traditional therapies. Recent studies have demonstrated the mechanisms and pathways that trigger or inhibit ferroptosis in CRC, and many regulatory molecules and pathways have been identified. Here, we review the current research progress on the mechanism of ferroptosis, new molecules that mediate ferroptosis, including coding and non-coding RNA; novel inducers and inhibitors of ferroptosis, which are mainly small-molecule compounds; and newly designed nanoparticles that increase the sensitivity of cells to ferroptosis. Finally, the gene signatures and clusters that have predictive value on CRC are summarized. |
format | Online Article Text |
id | pubmed-9821926 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-98219262023-01-07 Insights on Ferroptosis and Colorectal Cancer: Progress and Updates Hu, Bangli Yin, Yixin Li, Siqi Guo, Xianwen Molecules Review Patients with advanced-stage or treatment-resistant colorectal cancer (CRC) benefit less from traditional therapies; hence, new therapeutic strategies may help improve the treatment response and prognosis of these patients. Ferroptosis is an iron-dependent type of regulated cell death characterized by the accumulation of lipid reactive oxygen species (ROS), distinct from other types of regulated cell death. CRC cells, especially those with drug-resistant properties, are characterized by high iron levels and ROS. This indicates that the induction of ferroptosis in these cells may become a new therapeutic approach for CRC, particularly for eradicating CRC resistant to traditional therapies. Recent studies have demonstrated the mechanisms and pathways that trigger or inhibit ferroptosis in CRC, and many regulatory molecules and pathways have been identified. Here, we review the current research progress on the mechanism of ferroptosis, new molecules that mediate ferroptosis, including coding and non-coding RNA; novel inducers and inhibitors of ferroptosis, which are mainly small-molecule compounds; and newly designed nanoparticles that increase the sensitivity of cells to ferroptosis. Finally, the gene signatures and clusters that have predictive value on CRC are summarized. MDPI 2022-12-28 /pmc/articles/PMC9821926/ /pubmed/36615434 http://dx.doi.org/10.3390/molecules28010243 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Hu, Bangli Yin, Yixin Li, Siqi Guo, Xianwen Insights on Ferroptosis and Colorectal Cancer: Progress and Updates |
title | Insights on Ferroptosis and Colorectal Cancer: Progress and Updates |
title_full | Insights on Ferroptosis and Colorectal Cancer: Progress and Updates |
title_fullStr | Insights on Ferroptosis and Colorectal Cancer: Progress and Updates |
title_full_unstemmed | Insights on Ferroptosis and Colorectal Cancer: Progress and Updates |
title_short | Insights on Ferroptosis and Colorectal Cancer: Progress and Updates |
title_sort | insights on ferroptosis and colorectal cancer: progress and updates |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9821926/ https://www.ncbi.nlm.nih.gov/pubmed/36615434 http://dx.doi.org/10.3390/molecules28010243 |
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