Targeting Matrix Metalloproteinase-9 for Therapeutic Intervention in Diabetic Foot Ulcers.
Journal
ACS pharmacology & translational science
ISSN: 2575-9108
Titre abrégé: ACS Pharmacol Transl Sci
Pays: United States
ID NLM: 101721411
Informations de publication
Date de publication:
11 Oct 2024
11 Oct 2024
Historique:
received:
03
05
2024
revised:
26
06
2024
accepted:
28
06
2024
pmc-release:
16
07
2025
medline:
18
10
2024
pubmed:
18
10
2024
entrez:
18
10
2024
Statut:
epublish
Résumé
Diabetic foot ulcers (DFUs) are a complication of diabetes that have long been neglected. To date, a single drug (becaplermin containing platelet-derived growth factor, PDGF) has been approved by the FDA 27 years ago; however, it is seldom used because of its modest efficacy. The standard-of-care for DFUs is debridement, off-loading, and infection control with antibiotics, with hyperbaric oxygen (HBO) therapy being the treatment of last recourse. The paucity of understanding what accelerates diabetic wound healing results in more than 150,000 lower-limb amputations in the United States every year. A new paradigm for treatment of DFUs is proposed based on the higher levels of active matrix metalloproteinase (MMP)-9 with the more severe and infected human DFUs, and the demonstrated detrimental role of MMP-9 and the beneficial repair role of MMP-8 in diabetic mice. Selective inhibition of MMP-9 with the small molecule (
Identifiants
pubmed: 39421656
doi: 10.1021/acsptsci.4c00263
pmc: PMC11480886
doi:
Types de publication
Journal Article
Review
Langues
eng
Pagination
2901-2911Informations de copyright
© 2024 American Chemical Society.
Déclaration de conflit d'intérêts
The author declares the following competing financial interest(s): U.S. Patent 9,604,957, U.S. Patent 9,951,035, U.S. Patent 10,253,103, European Patent 3107905, Japan Patent 6,5,21,995, and China Patent ZL201580023723.6 have been issued for (R)-ND-336.