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Oxidative Stress, Nrf2, and Epigenetic Modification Contribute to Anticancer Drug Resistance
Nuclear factor E2-related factor 2 (Nrf2), a transcription factor, controls the expression of genes encoding cytoprotective proteins, including antioxidant enzymes that combat oxidative and electrophilic stress to maintain redox homeostasis. However, recent studies demonstrated that, in cancer, aber...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Korean Society of Toxicology
2017
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5266370/ https://www.ncbi.nlm.nih.gov/pubmed/28133507 http://dx.doi.org/10.5487/TR.2017.33.1.001 |
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author | Kang, Kyoung Ah Hyun, Jin Won |
author_facet | Kang, Kyoung Ah Hyun, Jin Won |
author_sort | Kang, Kyoung Ah |
collection | PubMed |
description | Nuclear factor E2-related factor 2 (Nrf2), a transcription factor, controls the expression of genes encoding cytoprotective proteins, including antioxidant enzymes that combat oxidative and electrophilic stress to maintain redox homeostasis. However, recent studies demonstrated that, in cancer, aberrant activation of Nrf2 by epigenetic alterations promotes high expression of cytoprotective proteins, which can decrease the efficacy of anticancer drugs used for chemotherapy. In this review, we summarize recent findings regarding the relationship between oxidative stress, Nrf2, epigenetic modification, and anticancer drug resistance, which should aid in development of new strategies to improve chemotherapeutic efficacy. |
format | Online Article Text |
id | pubmed-5266370 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Korean Society of Toxicology |
record_format | MEDLINE/PubMed |
spelling | pubmed-52663702017-01-27 Oxidative Stress, Nrf2, and Epigenetic Modification Contribute to Anticancer Drug Resistance Kang, Kyoung Ah Hyun, Jin Won Toxicol Res Invited Review Nuclear factor E2-related factor 2 (Nrf2), a transcription factor, controls the expression of genes encoding cytoprotective proteins, including antioxidant enzymes that combat oxidative and electrophilic stress to maintain redox homeostasis. However, recent studies demonstrated that, in cancer, aberrant activation of Nrf2 by epigenetic alterations promotes high expression of cytoprotective proteins, which can decrease the efficacy of anticancer drugs used for chemotherapy. In this review, we summarize recent findings regarding the relationship between oxidative stress, Nrf2, epigenetic modification, and anticancer drug resistance, which should aid in development of new strategies to improve chemotherapeutic efficacy. Korean Society of Toxicology 2017-01 2017-01-15 /pmc/articles/PMC5266370/ /pubmed/28133507 http://dx.doi.org/10.5487/TR.2017.33.1.001 Text en Copyright © 2017 The Korean Society Of Toxicology http://creativecommons.org/licenses/by-nc/3.0/ This is an Open-Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Invited Review Kang, Kyoung Ah Hyun, Jin Won Oxidative Stress, Nrf2, and Epigenetic Modification Contribute to Anticancer Drug Resistance |
title | Oxidative Stress, Nrf2, and Epigenetic Modification Contribute to Anticancer Drug Resistance |
title_full | Oxidative Stress, Nrf2, and Epigenetic Modification Contribute to Anticancer Drug Resistance |
title_fullStr | Oxidative Stress, Nrf2, and Epigenetic Modification Contribute to Anticancer Drug Resistance |
title_full_unstemmed | Oxidative Stress, Nrf2, and Epigenetic Modification Contribute to Anticancer Drug Resistance |
title_short | Oxidative Stress, Nrf2, and Epigenetic Modification Contribute to Anticancer Drug Resistance |
title_sort | oxidative stress, nrf2, and epigenetic modification contribute to anticancer drug resistance |
topic | Invited Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5266370/ https://www.ncbi.nlm.nih.gov/pubmed/28133507 http://dx.doi.org/10.5487/TR.2017.33.1.001 |
work_keys_str_mv | AT kangkyoungah oxidativestressnrf2andepigeneticmodificationcontributetoanticancerdrugresistance AT hyunjinwon oxidativestressnrf2andepigeneticmodificationcontributetoanticancerdrugresistance |