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The Role of NRF2/KEAP1 Signaling Pathway in Cancer Metabolism

The nuclear factor-erythroid 2 p45-related factor 2 (NRF2, also called Nfe2l2) and its cytoplasmic repressor, Kelch-like ECH-associated protein 1 (KEAP1), are major regulators of redox homeostasis controlling a multiple of genes for detoxification and cytoprotective enzymes. The NRF2/KEAP1 pathway i...

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Autores principales: Song, Moon-Young, Lee, Da-Young, Chun, Kyung-Soo, Kim, Eun-Hee
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8122702/
https://www.ncbi.nlm.nih.gov/pubmed/33922165
http://dx.doi.org/10.3390/ijms22094376
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author Song, Moon-Young
Lee, Da-Young
Chun, Kyung-Soo
Kim, Eun-Hee
author_facet Song, Moon-Young
Lee, Da-Young
Chun, Kyung-Soo
Kim, Eun-Hee
author_sort Song, Moon-Young
collection PubMed
description The nuclear factor-erythroid 2 p45-related factor 2 (NRF2, also called Nfe2l2) and its cytoplasmic repressor, Kelch-like ECH-associated protein 1 (KEAP1), are major regulators of redox homeostasis controlling a multiple of genes for detoxification and cytoprotective enzymes. The NRF2/KEAP1 pathway is a fundamental signaling cascade responsible for the resistance of metabolic, oxidative stress, inflammation, and anticancer effects. Interestingly, a recent accumulation of evidence has indicated that NRF2 exhibits an aberrant activation in cancer. Evidence has shown that the NRF2/KEAP1 signaling pathway is associated with the proliferation of cancer cells and tumerigenesis through metabolic reprogramming. In this review, we provide an overview of the regulatory molecular mechanism of the NRF2/KEAP1 pathway against metabolic reprogramming in cancer, suggesting that the regulation of NRF2/KEAP1 axis might approach as a novel therapeutic strategy for cancers.
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spelling pubmed-81227022021-05-16 The Role of NRF2/KEAP1 Signaling Pathway in Cancer Metabolism Song, Moon-Young Lee, Da-Young Chun, Kyung-Soo Kim, Eun-Hee Int J Mol Sci Review The nuclear factor-erythroid 2 p45-related factor 2 (NRF2, also called Nfe2l2) and its cytoplasmic repressor, Kelch-like ECH-associated protein 1 (KEAP1), are major regulators of redox homeostasis controlling a multiple of genes for detoxification and cytoprotective enzymes. The NRF2/KEAP1 pathway is a fundamental signaling cascade responsible for the resistance of metabolic, oxidative stress, inflammation, and anticancer effects. Interestingly, a recent accumulation of evidence has indicated that NRF2 exhibits an aberrant activation in cancer. Evidence has shown that the NRF2/KEAP1 signaling pathway is associated with the proliferation of cancer cells and tumerigenesis through metabolic reprogramming. In this review, we provide an overview of the regulatory molecular mechanism of the NRF2/KEAP1 pathway against metabolic reprogramming in cancer, suggesting that the regulation of NRF2/KEAP1 axis might approach as a novel therapeutic strategy for cancers. MDPI 2021-04-22 /pmc/articles/PMC8122702/ /pubmed/33922165 http://dx.doi.org/10.3390/ijms22094376 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Song, Moon-Young
Lee, Da-Young
Chun, Kyung-Soo
Kim, Eun-Hee
The Role of NRF2/KEAP1 Signaling Pathway in Cancer Metabolism
title The Role of NRF2/KEAP1 Signaling Pathway in Cancer Metabolism
title_full The Role of NRF2/KEAP1 Signaling Pathway in Cancer Metabolism
title_fullStr The Role of NRF2/KEAP1 Signaling Pathway in Cancer Metabolism
title_full_unstemmed The Role of NRF2/KEAP1 Signaling Pathway in Cancer Metabolism
title_short The Role of NRF2/KEAP1 Signaling Pathway in Cancer Metabolism
title_sort role of nrf2/keap1 signaling pathway in cancer metabolism
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8122702/
https://www.ncbi.nlm.nih.gov/pubmed/33922165
http://dx.doi.org/10.3390/ijms22094376
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