Matrix metalloproteinases in inflammation
- PMID: 24631662
- DOI: 10.1016/j.bbagen.2014.03.007
Matrix metalloproteinases in inflammation
Abstract
Background: Matrix metalloproteinases (MMPs) are a family of ubiquitously expressed zinc-dependent endopeptidases with broad substrate specificity and strictly regulated tissue specific expression. They are expressed in physiological situations and pathological conditions involving inflammation. MMPs regulate several functions related to inflammation including bioavailability and activity of inflammatory cytokines and chemokines. There is also evidence that MMPs regulate inflammation in tumor microenvironment, which plays an important role in cancer progression.
Scope of review: Here, we discuss the current view on the role of MMPs in the regulation of inflammation.
Major conclusions: MMPs modulate inflammation by regulating bioavailability and activity of cytokines, chemokines, and growth factors, as well as integrity of physical tissue barriers. MMPs are also involved in immune evasion of tumor cells and in regulation of inflammation in tumor microenvironment.
General significance: There is increasing evidence for non-matrix substrates of MMPs that are related to regulation of inflammatory processes. New methods have been employed for identification of the substrates of MMPs in inflammatory processes in vivo. Detailed information on the substrates of MMPs may offer more specific and effective ways of inhibiting MMP function by blocking the cleavage site in substrate or by inhibition of the bioactivity of the substrate. It is expected, that more precise information on the MMP-substrate interaction may offer novel strategies for therapeutic intervention in inflammatory diseases and cancer without blocking beneficial actions of MMPs. This article is part of a Special Issue entitled Matrix-mediated cell behaviour and properties.
Keywords: Cancer; Inflammation; Matrix; Proteinase; Signaling.
Copyright © 2014 Elsevier B.V. All rights reserved.
Similar articles
-
Next generation matrix metalloproteinase inhibitors - Novel strategies bring new prospects.Biochim Biophys Acta Mol Cell Res. 2017 Nov;1864(11 Pt A):1927-1939. doi: 10.1016/j.bbamcr.2017.06.009. Epub 2017 Jun 19. Biochim Biophys Acta Mol Cell Res. 2017. PMID: 28636874 Review.
-
The dual personalities of matrix metalloproteinases in inflammation.Front Biosci. 2007 Jan 1;12:1475-87. doi: 10.2741/2161. Front Biosci. 2007. PMID: 17127395 Review.
-
Matrix Metalloproteinases as Regulators of Periodontal Inflammation.Int J Mol Sci. 2017 Feb 17;18(2):440. doi: 10.3390/ijms18020440. Int J Mol Sci. 2017. PMID: 28218665 Free PMC article. Review.
-
Is there new hope for therapeutic matrix metalloproteinase inhibition?Nat Rev Drug Discov. 2014 Dec;13(12):904-27. doi: 10.1038/nrd4390. Epub 2014 Nov 7. Nat Rev Drug Discov. 2014. PMID: 25376097 Review.
-
Biochemical and Biological Attributes of Matrix Metalloproteinases.Prog Mol Biol Transl Sci. 2017;147:1-73. doi: 10.1016/bs.pmbts.2017.02.005. Epub 2017 Mar 22. Prog Mol Biol Transl Sci. 2017. PMID: 28413025 Free PMC article. Review.
Cited by
-
Biomarkers of Bipolar Disorder in Late Life: An Evidence-Based Systematic Review.Curr Psychiatry Rep. 2024 Mar 12. doi: 10.1007/s11920-024-01483-7. Online ahead of print. Curr Psychiatry Rep. 2024. PMID: 38470559 Review.
-
Study on the rationality of small diameter metallic airway stent in treatment of tracheal stenosis in injured rabbits.J Cardiothorac Surg. 2024 Mar 5;19(1):110. doi: 10.1186/s13019-023-02470-4. J Cardiothorac Surg. 2024. PMID: 38443931 Free PMC article.
-
Resistance training modifies of serum levels of matrix metalloproteinase 2 and tissue inhibitor of matrix metalloproteinases in multiple sclerosis women - a randomized controlled trail.BMC Neurosci. 2024 Mar 4;25(1):13. doi: 10.1186/s12868-024-00856-1. BMC Neurosci. 2024. PMID: 38438999 Free PMC article. Clinical Trial.
-
Matrix metalloproteinase-8 regulates dendritic cell tolerance in late polymicrobial sepsis via the nuclear factor kappa-B p65/β-catenin pathway.Burns Trauma. 2024 Feb 28;12:tkad025. doi: 10.1093/burnst/tkad025. eCollection 2024. Burns Trauma. 2024. PMID: 38425412 Free PMC article.
-
Effects of barakol from Cassia siamea on neuroblastoma SH-SY5Y cell line: A potential combined therapy with doxorubicin.Heliyon. 2024 Jan 19;10(3):e24694. doi: 10.1016/j.heliyon.2024.e24694. eCollection 2024 Feb 15. Heliyon. 2024. PMID: 38318050 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Research Materials
