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Regulation of Wound Healing by the NRF2 Transcription Factor—More Than Cytoprotection
The nuclear factor-erythroid 2-related factor 2 (NRF2) transcription factor plays a central role in mediating the cellular stress response. Due to their antioxidant properties, compounds activating NRF2 have received much attention as potential medications for disease prevention, or even for therapy...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6720615/ https://www.ncbi.nlm.nih.gov/pubmed/31398789 http://dx.doi.org/10.3390/ijms20163856 |
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author | Hiebert, Paul Werner, Sabine |
author_facet | Hiebert, Paul Werner, Sabine |
author_sort | Hiebert, Paul |
collection | PubMed |
description | The nuclear factor-erythroid 2-related factor 2 (NRF2) transcription factor plays a central role in mediating the cellular stress response. Due to their antioxidant properties, compounds activating NRF2 have received much attention as potential medications for disease prevention, or even for therapy. Accumulating evidence suggests that activation of the NRF2 pathway also has a major impact on wound healing and may be beneficial in the treatment of chronic wounds, which remain a considerable health and economic burden. While NRF2 activation indeed shows promise, important considerations need to be made in light of corresponding evidence that also points towards pro-tumorigenic effects of NRF2. In this review, we discuss the evidence to date, highlighting recent advances using gain- and loss-of-function animal models and how these data fit with observations in humans. |
format | Online Article Text |
id | pubmed-6720615 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-67206152019-09-10 Regulation of Wound Healing by the NRF2 Transcription Factor—More Than Cytoprotection Hiebert, Paul Werner, Sabine Int J Mol Sci Review The nuclear factor-erythroid 2-related factor 2 (NRF2) transcription factor plays a central role in mediating the cellular stress response. Due to their antioxidant properties, compounds activating NRF2 have received much attention as potential medications for disease prevention, or even for therapy. Accumulating evidence suggests that activation of the NRF2 pathway also has a major impact on wound healing and may be beneficial in the treatment of chronic wounds, which remain a considerable health and economic burden. While NRF2 activation indeed shows promise, important considerations need to be made in light of corresponding evidence that also points towards pro-tumorigenic effects of NRF2. In this review, we discuss the evidence to date, highlighting recent advances using gain- and loss-of-function animal models and how these data fit with observations in humans. MDPI 2019-08-08 /pmc/articles/PMC6720615/ /pubmed/31398789 http://dx.doi.org/10.3390/ijms20163856 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 Hiebert, Paul Werner, Sabine Regulation of Wound Healing by the NRF2 Transcription Factor—More Than Cytoprotection |
title | Regulation of Wound Healing by the NRF2 Transcription Factor—More Than Cytoprotection |
title_full | Regulation of Wound Healing by the NRF2 Transcription Factor—More Than Cytoprotection |
title_fullStr | Regulation of Wound Healing by the NRF2 Transcription Factor—More Than Cytoprotection |
title_full_unstemmed | Regulation of Wound Healing by the NRF2 Transcription Factor—More Than Cytoprotection |
title_short | Regulation of Wound Healing by the NRF2 Transcription Factor—More Than Cytoprotection |
title_sort | regulation of wound healing by the nrf2 transcription factor—more than cytoprotection |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6720615/ https://www.ncbi.nlm.nih.gov/pubmed/31398789 http://dx.doi.org/10.3390/ijms20163856 |
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