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Therapeutic Targeting of the NRF2 Signaling Pathway in Cancer
Cancer is one of the most fatal diseases with an increasing incidence and mortality all over the world. Thus, there is an urgent need for novel therapies targeting major cancer-related pathways. Nuclear factor-erythroid 2-related factor 2 (NRF2) and its major negative modulator Kelch-like ECH-associ...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7961421/ https://www.ncbi.nlm.nih.gov/pubmed/33808001 http://dx.doi.org/10.3390/molecules26051417 |
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author | Telkoparan-Akillilar, Pelin Panieri, Emiliano Cevik, Dilek Suzen, Sibel Saso, Luciano |
author_facet | Telkoparan-Akillilar, Pelin Panieri, Emiliano Cevik, Dilek Suzen, Sibel Saso, Luciano |
author_sort | Telkoparan-Akillilar, Pelin |
collection | PubMed |
description | Cancer is one of the most fatal diseases with an increasing incidence and mortality all over the world. Thus, there is an urgent need for novel therapies targeting major cancer-related pathways. Nuclear factor-erythroid 2-related factor 2 (NRF2) and its major negative modulator Kelch-like ECH-associated protein 1 (KEAP1) are main players of the cellular defense mechanisms against internal and external cell stressors. However, NRF2/KEAP1 signaling pathway is dysregulated in various cancers, thus promoting tumor cell survival and metastasis. In the present review, we discuss the mechanisms of normal and deregulated NRF2 signaling pathway focusing on its cancer-related functions. We further explore activators and inhibitors of this pathway as cancer targeting drug candidates in order to provide an extensive background on the subject. |
format | Online Article Text |
id | pubmed-7961421 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-79614212021-03-17 Therapeutic Targeting of the NRF2 Signaling Pathway in Cancer Telkoparan-Akillilar, Pelin Panieri, Emiliano Cevik, Dilek Suzen, Sibel Saso, Luciano Molecules Review Cancer is one of the most fatal diseases with an increasing incidence and mortality all over the world. Thus, there is an urgent need for novel therapies targeting major cancer-related pathways. Nuclear factor-erythroid 2-related factor 2 (NRF2) and its major negative modulator Kelch-like ECH-associated protein 1 (KEAP1) are main players of the cellular defense mechanisms against internal and external cell stressors. However, NRF2/KEAP1 signaling pathway is dysregulated in various cancers, thus promoting tumor cell survival and metastasis. In the present review, we discuss the mechanisms of normal and deregulated NRF2 signaling pathway focusing on its cancer-related functions. We further explore activators and inhibitors of this pathway as cancer targeting drug candidates in order to provide an extensive background on the subject. MDPI 2021-03-05 /pmc/articles/PMC7961421/ /pubmed/33808001 http://dx.doi.org/10.3390/molecules26051417 Text en © 2021 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 Panieri, Emiliano Cevik, Dilek Suzen, Sibel Saso, Luciano Therapeutic Targeting of the NRF2 Signaling Pathway in Cancer |
title | Therapeutic Targeting of the NRF2 Signaling Pathway in Cancer |
title_full | Therapeutic Targeting of the NRF2 Signaling Pathway in Cancer |
title_fullStr | Therapeutic Targeting of the NRF2 Signaling Pathway in Cancer |
title_full_unstemmed | Therapeutic Targeting of the NRF2 Signaling Pathway in Cancer |
title_short | Therapeutic Targeting of the NRF2 Signaling Pathway in Cancer |
title_sort | therapeutic targeting of the nrf2 signaling pathway in cancer |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7961421/ https://www.ncbi.nlm.nih.gov/pubmed/33808001 http://dx.doi.org/10.3390/molecules26051417 |
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