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Design and development of Nrf2 modulators for cancer chemoprevention and therapy: a review

A major cell defense mechanism against oxidative and xenobiotic stress is mediated by the Nrf2/Keap1 signaling pathway. The Nrf2/Keap1 pathway regulates gene expression of many cytoprotective and detoxifying enzymes, thus playing a pivotal role in maintaining redox cellular homeostasis. Many disease...

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Autores principales: Sova, Matej, Saso, Luciano
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6161735/
https://www.ncbi.nlm.nih.gov/pubmed/30288023
http://dx.doi.org/10.2147/DDDT.S172612
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author Sova, Matej
Saso, Luciano
author_facet Sova, Matej
Saso, Luciano
author_sort Sova, Matej
collection PubMed
description A major cell defense mechanism against oxidative and xenobiotic stress is mediated by the Nrf2/Keap1 signaling pathway. The Nrf2/Keap1 pathway regulates gene expression of many cytoprotective and detoxifying enzymes, thus playing a pivotal role in maintaining redox cellular homeostasis. Many diseases including cancer have been closely related to impaired Nrf2 activity. Targeting Nrf2 and modulating its activity represents a novel modern strategy for cancer chemoprevention and therapy. In this review, different design strategies used for the development of Nrf2 modulators are described in detail. Moreover, the main focus is on important and recently developed Nrf2 activators and inhibitors, their in vitro and in vivo studies, and their potential use as chemopreventive agents and/or cancer therapeutics.
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spelling pubmed-61617352018-10-04 Design and development of Nrf2 modulators for cancer chemoprevention and therapy: a review Sova, Matej Saso, Luciano Drug Des Devel Ther Review A major cell defense mechanism against oxidative and xenobiotic stress is mediated by the Nrf2/Keap1 signaling pathway. The Nrf2/Keap1 pathway regulates gene expression of many cytoprotective and detoxifying enzymes, thus playing a pivotal role in maintaining redox cellular homeostasis. Many diseases including cancer have been closely related to impaired Nrf2 activity. Targeting Nrf2 and modulating its activity represents a novel modern strategy for cancer chemoprevention and therapy. In this review, different design strategies used for the development of Nrf2 modulators are described in detail. Moreover, the main focus is on important and recently developed Nrf2 activators and inhibitors, their in vitro and in vivo studies, and their potential use as chemopreventive agents and/or cancer therapeutics. Dove Medical Press 2018-09-25 /pmc/articles/PMC6161735/ /pubmed/30288023 http://dx.doi.org/10.2147/DDDT.S172612 Text en © 2018 Sova and Saso. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Review
Sova, Matej
Saso, Luciano
Design and development of Nrf2 modulators for cancer chemoprevention and therapy: a review
title Design and development of Nrf2 modulators for cancer chemoprevention and therapy: a review
title_full Design and development of Nrf2 modulators for cancer chemoprevention and therapy: a review
title_fullStr Design and development of Nrf2 modulators for cancer chemoprevention and therapy: a review
title_full_unstemmed Design and development of Nrf2 modulators for cancer chemoprevention and therapy: a review
title_short Design and development of Nrf2 modulators for cancer chemoprevention and therapy: a review
title_sort design and development of nrf2 modulators for cancer chemoprevention and therapy: a review
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6161735/
https://www.ncbi.nlm.nih.gov/pubmed/30288023
http://dx.doi.org/10.2147/DDDT.S172612
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