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Pharmacological Applications of Nrf2 Inhibitors as Potential Antineoplastic Drugs

Oxidative stress (OS) is associated with many diseases ranging from cancer to neurodegenerative disorders. Nuclear factor-erythroid 2 p45-related factor 2 (Nrf2) is one of the most effective cytoprotective controller against OS. Modulation of Nrf2 pathway constitutes a remarkable strategy in the ant...

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Autores principales: Telkoparan-Akillilar, Pelin, Suzen, Sibel, Saso, Luciano
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6514836/
https://www.ncbi.nlm.nih.gov/pubmed/31022969
http://dx.doi.org/10.3390/ijms20082025
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author Telkoparan-Akillilar, Pelin
Suzen, Sibel
Saso, Luciano
author_facet Telkoparan-Akillilar, Pelin
Suzen, Sibel
Saso, Luciano
author_sort Telkoparan-Akillilar, Pelin
collection PubMed
description Oxidative stress (OS) is associated with many diseases ranging from cancer to neurodegenerative disorders. Nuclear factor-erythroid 2 p45-related factor 2 (Nrf2) is one of the most effective cytoprotective controller against OS. Modulation of Nrf2 pathway constitutes a remarkable strategy in the antineoplastic treatments. A big number of Nrf2-antioxidant response element activators have been screened for use as chemo-preventive drugs in OS associated diseases like cancer even though activation of Nrf2 happens in a variety of cancers. Research proved that hyperactivation of the Nrf2 pathway produces a situation that helps the survival of normal as well as malignant cells, protecting them against OS, anticancer drugs, and radiotherapy. In this review, the modulation of the Nrf2 pathway, anticancer activity and challenges associated with the development of an Nrf2-based anti-cancer treatment approaches are discussed.
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spelling pubmed-65148362019-05-30 Pharmacological Applications of Nrf2 Inhibitors as Potential Antineoplastic Drugs Telkoparan-Akillilar, Pelin Suzen, Sibel Saso, Luciano Int J Mol Sci Review Oxidative stress (OS) is associated with many diseases ranging from cancer to neurodegenerative disorders. Nuclear factor-erythroid 2 p45-related factor 2 (Nrf2) is one of the most effective cytoprotective controller against OS. Modulation of Nrf2 pathway constitutes a remarkable strategy in the antineoplastic treatments. A big number of Nrf2-antioxidant response element activators have been screened for use as chemo-preventive drugs in OS associated diseases like cancer even though activation of Nrf2 happens in a variety of cancers. Research proved that hyperactivation of the Nrf2 pathway produces a situation that helps the survival of normal as well as malignant cells, protecting them against OS, anticancer drugs, and radiotherapy. In this review, the modulation of the Nrf2 pathway, anticancer activity and challenges associated with the development of an Nrf2-based anti-cancer treatment approaches are discussed. MDPI 2019-04-24 /pmc/articles/PMC6514836/ /pubmed/31022969 http://dx.doi.org/10.3390/ijms20082025 Text en © 2019 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Telkoparan-Akillilar, Pelin
Suzen, Sibel
Saso, Luciano
Pharmacological Applications of Nrf2 Inhibitors as Potential Antineoplastic Drugs
title Pharmacological Applications of Nrf2 Inhibitors as Potential Antineoplastic Drugs
title_full Pharmacological Applications of Nrf2 Inhibitors as Potential Antineoplastic Drugs
title_fullStr Pharmacological Applications of Nrf2 Inhibitors as Potential Antineoplastic Drugs
title_full_unstemmed Pharmacological Applications of Nrf2 Inhibitors as Potential Antineoplastic Drugs
title_short Pharmacological Applications of Nrf2 Inhibitors as Potential Antineoplastic Drugs
title_sort pharmacological applications of nrf2 inhibitors as potential antineoplastic drugs
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6514836/
https://www.ncbi.nlm.nih.gov/pubmed/31022969
http://dx.doi.org/10.3390/ijms20082025
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