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mTOR-Mediated Antioxidant Activation in Solid Tumor Radioresistance
Radiotherapy is widely used for the treatment of cancer patients, but tumor radioresistance presents serious therapy challenges. Tumor radioresistance is closely related to high levels of mTOR signaling in tumor tissues. Therefore, targeting the mTOR pathway might be a strategy to promote solid tumo...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6942807/ https://www.ncbi.nlm.nih.gov/pubmed/31929797 http://dx.doi.org/10.1155/2019/5956867 |
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author | Woo, Yunseo Lee, Hyo-Ji Jung, Young Mee Jung, Yu-Jin |
author_facet | Woo, Yunseo Lee, Hyo-Ji Jung, Young Mee Jung, Yu-Jin |
author_sort | Woo, Yunseo |
collection | PubMed |
description | Radiotherapy is widely used for the treatment of cancer patients, but tumor radioresistance presents serious therapy challenges. Tumor radioresistance is closely related to high levels of mTOR signaling in tumor tissues. Therefore, targeting the mTOR pathway might be a strategy to promote solid tumor sensitivity to ionizing radiation. Radioresistance is associated with enhanced antioxidant mechanisms in cancer cells. Therefore, examination of the relationship between mTOR signaling and antioxidant mechanism-linked radioresistance is required for effective radiotherapy. In particular, the effect of mTOR signaling on antioxidant glutathione induction by the Keap1-NRF2-xCT pathway is described in this review. This review is expected to assist in the identification of therapeutic adjuvants to increase the efficacy of radiotherapy. |
format | Online Article Text |
id | pubmed-6942807 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-69428072020-01-10 mTOR-Mediated Antioxidant Activation in Solid Tumor Radioresistance Woo, Yunseo Lee, Hyo-Ji Jung, Young Mee Jung, Yu-Jin J Oncol Review Article Radiotherapy is widely used for the treatment of cancer patients, but tumor radioresistance presents serious therapy challenges. Tumor radioresistance is closely related to high levels of mTOR signaling in tumor tissues. Therefore, targeting the mTOR pathway might be a strategy to promote solid tumor sensitivity to ionizing radiation. Radioresistance is associated with enhanced antioxidant mechanisms in cancer cells. Therefore, examination of the relationship between mTOR signaling and antioxidant mechanism-linked radioresistance is required for effective radiotherapy. In particular, the effect of mTOR signaling on antioxidant glutathione induction by the Keap1-NRF2-xCT pathway is described in this review. This review is expected to assist in the identification of therapeutic adjuvants to increase the efficacy of radiotherapy. Hindawi 2019-12-20 /pmc/articles/PMC6942807/ /pubmed/31929797 http://dx.doi.org/10.1155/2019/5956867 Text en Copyright © 2019 Yunseo Woo et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Review Article Woo, Yunseo Lee, Hyo-Ji Jung, Young Mee Jung, Yu-Jin mTOR-Mediated Antioxidant Activation in Solid Tumor Radioresistance |
title | mTOR-Mediated Antioxidant Activation in Solid Tumor Radioresistance |
title_full | mTOR-Mediated Antioxidant Activation in Solid Tumor Radioresistance |
title_fullStr | mTOR-Mediated Antioxidant Activation in Solid Tumor Radioresistance |
title_full_unstemmed | mTOR-Mediated Antioxidant Activation in Solid Tumor Radioresistance |
title_short | mTOR-Mediated Antioxidant Activation in Solid Tumor Radioresistance |
title_sort | mtor-mediated antioxidant activation in solid tumor radioresistance |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6942807/ https://www.ncbi.nlm.nih.gov/pubmed/31929797 http://dx.doi.org/10.1155/2019/5956867 |
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