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Targeting MMP-9 in Diabetic Foot Ulcers
Diabetic foot ulcers (DFUs) are significant complications of diabetes and an unmet medical need. Matrix metalloproteinases (MMPs) play important roles in the pathology of wounds and in the wound healing process. However, because of the challenge in distinguishing active MMPs from the two catalytical...
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/PMC6630664/ https://www.ncbi.nlm.nih.gov/pubmed/31121851 http://dx.doi.org/10.3390/ph12020079 |
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author | Jones, Jeffrey I. Nguyen, Trung T. Peng, Zhihong Chang, Mayland |
author_facet | Jones, Jeffrey I. Nguyen, Trung T. Peng, Zhihong Chang, Mayland |
author_sort | Jones, Jeffrey I. |
collection | PubMed |
description | Diabetic foot ulcers (DFUs) are significant complications of diabetes and an unmet medical need. Matrix metalloproteinases (MMPs) play important roles in the pathology of wounds and in the wound healing process. However, because of the challenge in distinguishing active MMPs from the two catalytically inactive forms of MMPs and the clinical failure of broad-spectrum MMP inhibitors in cancer, MMPs have not been a target for treatment of DFUs until recently. This review covers the discovery of active MMP-9 as the biochemical culprit in the recalcitrance of diabetic wounds to healing and targeting this proteinase as a novel approach for the treatment of DFUs. Active MMP-8 and MMP-9 were observed in mouse and human diabetic wounds using a batimastat affinity resin and proteomics. MMP-9 was shown to play a detrimental role in diabetic wound healing, whereas MMP-8 was beneficial. A new class of selective MMP-9 inhibitors shows clinical promise for the treatment of DFUs. |
format | Online Article Text |
id | pubmed-6630664 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-66306642019-08-19 Targeting MMP-9 in Diabetic Foot Ulcers Jones, Jeffrey I. Nguyen, Trung T. Peng, Zhihong Chang, Mayland Pharmaceuticals (Basel) Review Diabetic foot ulcers (DFUs) are significant complications of diabetes and an unmet medical need. Matrix metalloproteinases (MMPs) play important roles in the pathology of wounds and in the wound healing process. However, because of the challenge in distinguishing active MMPs from the two catalytically inactive forms of MMPs and the clinical failure of broad-spectrum MMP inhibitors in cancer, MMPs have not been a target for treatment of DFUs until recently. This review covers the discovery of active MMP-9 as the biochemical culprit in the recalcitrance of diabetic wounds to healing and targeting this proteinase as a novel approach for the treatment of DFUs. Active MMP-8 and MMP-9 were observed in mouse and human diabetic wounds using a batimastat affinity resin and proteomics. MMP-9 was shown to play a detrimental role in diabetic wound healing, whereas MMP-8 was beneficial. A new class of selective MMP-9 inhibitors shows clinical promise for the treatment of DFUs. MDPI 2019-05-22 /pmc/articles/PMC6630664/ /pubmed/31121851 http://dx.doi.org/10.3390/ph12020079 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 Jones, Jeffrey I. Nguyen, Trung T. Peng, Zhihong Chang, Mayland Targeting MMP-9 in Diabetic Foot Ulcers |
title | Targeting MMP-9 in Diabetic Foot Ulcers |
title_full | Targeting MMP-9 in Diabetic Foot Ulcers |
title_fullStr | Targeting MMP-9 in Diabetic Foot Ulcers |
title_full_unstemmed | Targeting MMP-9 in Diabetic Foot Ulcers |
title_short | Targeting MMP-9 in Diabetic Foot Ulcers |
title_sort | targeting mmp-9 in diabetic foot ulcers |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6630664/ https://www.ncbi.nlm.nih.gov/pubmed/31121851 http://dx.doi.org/10.3390/ph12020079 |
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