Matrix Metalloproteases as Influencers of the Cells' Social Media.


Journal

International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791

Informations de publication

Date de publication:
07 Aug 2019
Historique:
received: 08 07 2019
revised: 01 08 2019
accepted: 02 08 2019
entrez: 10 8 2019
pubmed: 10 8 2019
medline: 7 1 2020
Statut: epublish

Résumé

Matrix metalloproteinases (MMPs) have been studied in the context of cancer due to their ability to increase cell invasion, and were initially thought to facilitate metastasis solely through the degradation of the extracellular matrix (ECM). MMPs have also been investigated in the context of their ECM remodeling activity in several acute and chronic inflammatory diseases. However, after several MMP inhibitors failed in phase III clinical trials, a global reassessment of their biological functions was undertaken, which has revealed multiple unanticipated functions including the processing of chemokines, cytokines, and cell surface receptors. Despite what their name suggests, the matrix aspect of MMPs could contribute to a lesser part of their physiological functions in inflammatory diseases, as originally anticipated. Here, we present examples of MMP substrates implicated in cell signaling, independent of their ECM functions, and discuss the impact for the use of MMP inhibitors.

Identifiants

pubmed: 31394726
pii: ijms20163847
doi: 10.3390/ijms20163847
pmc: PMC6720954
pii:
doi:

Substances chimiques

Cytokines 0
fas Receptor 0
Matrix Metalloproteinases EC 3.4.24.-

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

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Auteurs

Daniel Young (D)

Department of Physiology and Pharmacology, University of Calgary, Calgary, AB T2N 4N1, Canada.
McCaig Institute for Bone and Joint Health, University of Calgary, Calgary, AB T2N 4N1, Canada.

Nabangshu Das (N)

McCaig Institute for Bone and Joint Health, University of Calgary, Calgary, AB T2N 4N1, Canada.
Faculty of Kinesiology, University of Calgary, Calgary, AB T2N 4N1, Canada.

Anthonia Anowai (A)

Department of Physiology and Pharmacology, University of Calgary, Calgary, AB T2N 4N1, Canada.
McCaig Institute for Bone and Joint Health, University of Calgary, Calgary, AB T2N 4N1, Canada.
Department of Biochemistry and Molecular Biology, University of Calgary, Calgary, AB T2N 4N1, Canada.

Antoine Dufour (A)

Department of Physiology and Pharmacology, University of Calgary, Calgary, AB T2N 4N1, Canada. antoine.dufour@ucalgary.ca.
McCaig Institute for Bone and Joint Health, University of Calgary, Calgary, AB T2N 4N1, Canada. antoine.dufour@ucalgary.ca.
Faculty of Kinesiology, University of Calgary, Calgary, AB T2N 4N1, Canada. antoine.dufour@ucalgary.ca.
Department of Biochemistry and Molecular Biology, University of Calgary, Calgary, AB T2N 4N1, Canada. antoine.dufour@ucalgary.ca.

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