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Nuclear Factor Erythroid 2-Related Factor 2 in Regulating Cancer Metabolism

Significance: Nuclear factor erythroid 2 (NFE2)-related factor 2 (NFE2L2, or NRF2) is a transcription factor predominantly affecting the expression of antioxidant genes. NRF2 plays a significant role in the control of redox balance, which is crucial in cancer cells. NRF2 activation regulates numerou...

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Autores principales: Smolková, Katarína, Mikó, Edit, Kovács, Tünde, Leguina-Ruzzi, Alberto, Sipos, Adrienn, Bai, Péter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Mary Ann Liebert, Inc., publishers 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7533893/
https://www.ncbi.nlm.nih.gov/pubmed/31989830
http://dx.doi.org/10.1089/ars.2020.8024
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author Smolková, Katarína
Mikó, Edit
Kovács, Tünde
Leguina-Ruzzi, Alberto
Sipos, Adrienn
Bai, Péter
author_facet Smolková, Katarína
Mikó, Edit
Kovács, Tünde
Leguina-Ruzzi, Alberto
Sipos, Adrienn
Bai, Péter
author_sort Smolková, Katarína
collection PubMed
description Significance: Nuclear factor erythroid 2 (NFE2)-related factor 2 (NFE2L2, or NRF2) is a transcription factor predominantly affecting the expression of antioxidant genes. NRF2 plays a significant role in the control of redox balance, which is crucial in cancer cells. NRF2 activation regulates numerous cancer hallmarks, including metabolism, cancer stem cell characteristics, tumor aggressiveness, invasion, and metastasis formation. We review the molecular characteristics of the NRF2 pathway and discuss its interactions with the cancer hallmarks previously listed. Recent Advances: The noncanonical activation of NRF2 was recently discovered, and members of this pathway are involved in carcinogenesis. Further, cancer-related changes (e.g., metabolic flexibility) that support cancer progression were found to be redox- and NRF2 dependent. Critical Issues: NRF2 undergoes Janus-faced behavior in cancers. The pro- or antineoplastic effects of NRF2 are context dependent and essentially based on the specific molecular characteristics of the cancer in question. Therefore, systematic investigation of NRF2 signaling is necessary to clarify its role in cancer etiology. The biggest challenge in the NRF2 field is to determine which cancers can be targeted for better clinical outcomes. Further, large-scale genomic and transcriptomic studies are missing to correlate the clinical outcome with the activity of the NRF2 system. Future Directions: To exploit NRF2 in a clinical setting in the future, the druggable members of the NRF2 pathway should be identified. In addition, it will be important to study how the modulation of the NRF2 system interferes with cytostatic drugs and their combinations.
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spelling pubmed-75338932020-10-05 Nuclear Factor Erythroid 2-Related Factor 2 in Regulating Cancer Metabolism Smolková, Katarína Mikó, Edit Kovács, Tünde Leguina-Ruzzi, Alberto Sipos, Adrienn Bai, Péter Antioxid Redox Signal Forum Review Articles Significance: Nuclear factor erythroid 2 (NFE2)-related factor 2 (NFE2L2, or NRF2) is a transcription factor predominantly affecting the expression of antioxidant genes. NRF2 plays a significant role in the control of redox balance, which is crucial in cancer cells. NRF2 activation regulates numerous cancer hallmarks, including metabolism, cancer stem cell characteristics, tumor aggressiveness, invasion, and metastasis formation. We review the molecular characteristics of the NRF2 pathway and discuss its interactions with the cancer hallmarks previously listed. Recent Advances: The noncanonical activation of NRF2 was recently discovered, and members of this pathway are involved in carcinogenesis. Further, cancer-related changes (e.g., metabolic flexibility) that support cancer progression were found to be redox- and NRF2 dependent. Critical Issues: NRF2 undergoes Janus-faced behavior in cancers. The pro- or antineoplastic effects of NRF2 are context dependent and essentially based on the specific molecular characteristics of the cancer in question. Therefore, systematic investigation of NRF2 signaling is necessary to clarify its role in cancer etiology. The biggest challenge in the NRF2 field is to determine which cancers can be targeted for better clinical outcomes. Further, large-scale genomic and transcriptomic studies are missing to correlate the clinical outcome with the activity of the NRF2 system. Future Directions: To exploit NRF2 in a clinical setting in the future, the druggable members of the NRF2 pathway should be identified. In addition, it will be important to study how the modulation of the NRF2 system interferes with cytostatic drugs and their combinations. Mary Ann Liebert, Inc., publishers 2020-11-01 2020-09-29 /pmc/articles/PMC7533893/ /pubmed/31989830 http://dx.doi.org/10.1089/ars.2020.8024 Text en © Katarína Smolková et al. 2020; Published by Mary Ann Liebert, Inc. This Open Access article is distributed under the terms of the Creative Commons Attribution Noncommercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and the source are cited.
spellingShingle Forum Review Articles
Smolková, Katarína
Mikó, Edit
Kovács, Tünde
Leguina-Ruzzi, Alberto
Sipos, Adrienn
Bai, Péter
Nuclear Factor Erythroid 2-Related Factor 2 in Regulating Cancer Metabolism
title Nuclear Factor Erythroid 2-Related Factor 2 in Regulating Cancer Metabolism
title_full Nuclear Factor Erythroid 2-Related Factor 2 in Regulating Cancer Metabolism
title_fullStr Nuclear Factor Erythroid 2-Related Factor 2 in Regulating Cancer Metabolism
title_full_unstemmed Nuclear Factor Erythroid 2-Related Factor 2 in Regulating Cancer Metabolism
title_short Nuclear Factor Erythroid 2-Related Factor 2 in Regulating Cancer Metabolism
title_sort nuclear factor erythroid 2-related factor 2 in regulating cancer metabolism
topic Forum Review Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7533893/
https://www.ncbi.nlm.nih.gov/pubmed/31989830
http://dx.doi.org/10.1089/ars.2020.8024
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