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Regulation of Nrf2-Mediated Phase II Detoxification and Anti-oxidant Genes

The molecular mechanisms by which a variety of naturally-occurring dietary compounds exert chemopreventive effects have been a subject of intense scientific investigations. Induction of phase II detoxification and anti-oxidant enzymes through activation of Nrf2/ARE-dependent gene is recognized as on...

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Autor principal: Keum, Young-Sam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society of Applied Pharmacology 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3792210/
https://www.ncbi.nlm.nih.gov/pubmed/24116287
http://dx.doi.org/10.4062/biomolther.2012.20.2.144
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author Keum, Young-Sam
author_facet Keum, Young-Sam
author_sort Keum, Young-Sam
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description The molecular mechanisms by which a variety of naturally-occurring dietary compounds exert chemopreventive effects have been a subject of intense scientific investigations. Induction of phase II detoxification and anti-oxidant enzymes through activation of Nrf2/ARE-dependent gene is recognized as one of the major cellular defense mechanisms against oxidative or xenobiotic stresses and currently represents a critical chemopreventive mechanism of action. In the present review, the functional significance of Keap1/Nrf2 protein module in regulating ARE-dependent phase II detoxification and anti-oxidant gene expression is discussed. The biochemical mechanisms underlying the phosphorylation and expression of Keap1/Nrf2 proteins that are controlled by the intracellular signaling kinases and ubiquitin-mediated E3 ligase system as well as control of nucleocytoplasmic translocation of Nrf2 by its innate nuclear export signal (NES) are described.
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spelling pubmed-37922102013-10-10 Regulation of Nrf2-Mediated Phase II Detoxification and Anti-oxidant Genes Keum, Young-Sam Biomol Ther (Seoul) Articles The molecular mechanisms by which a variety of naturally-occurring dietary compounds exert chemopreventive effects have been a subject of intense scientific investigations. Induction of phase II detoxification and anti-oxidant enzymes through activation of Nrf2/ARE-dependent gene is recognized as one of the major cellular defense mechanisms against oxidative or xenobiotic stresses and currently represents a critical chemopreventive mechanism of action. In the present review, the functional significance of Keap1/Nrf2 protein module in regulating ARE-dependent phase II detoxification and anti-oxidant gene expression is discussed. The biochemical mechanisms underlying the phosphorylation and expression of Keap1/Nrf2 proteins that are controlled by the intracellular signaling kinases and ubiquitin-mediated E3 ligase system as well as control of nucleocytoplasmic translocation of Nrf2 by its innate nuclear export signal (NES) are described. The Korean Society of Applied Pharmacology 2012-03 /pmc/articles/PMC3792210/ /pubmed/24116287 http://dx.doi.org/10.4062/biomolther.2012.20.2.144 Text en Copyright ©2012, The Korean Society of Applied Pharmacology 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 Articles
Keum, Young-Sam
Regulation of Nrf2-Mediated Phase II Detoxification and Anti-oxidant Genes
title Regulation of Nrf2-Mediated Phase II Detoxification and Anti-oxidant Genes
title_full Regulation of Nrf2-Mediated Phase II Detoxification and Anti-oxidant Genes
title_fullStr Regulation of Nrf2-Mediated Phase II Detoxification and Anti-oxidant Genes
title_full_unstemmed Regulation of Nrf2-Mediated Phase II Detoxification and Anti-oxidant Genes
title_short Regulation of Nrf2-Mediated Phase II Detoxification and Anti-oxidant Genes
title_sort regulation of nrf2-mediated phase ii detoxification and anti-oxidant genes
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3792210/
https://www.ncbi.nlm.nih.gov/pubmed/24116287
http://dx.doi.org/10.4062/biomolther.2012.20.2.144
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