Tumour microenvironment - opinion: validating matrix metalloproteinases as drug targets and anti-targets for cancer therapy
- PMID: 16498445
- DOI: 10.1038/nrc1821
Tumour microenvironment - opinion: validating matrix metalloproteinases as drug targets and anti-targets for cancer therapy
Abstract
The matrix metalloproteinases (MMPs) mediate homeostasis of the extracellular environment. They have multiple signalling activities that are commonly altered during tumorigenesis and that might serve as intervention points for anticancer drugs. However, there are many criteria to consider in validating MMPs as drug targets and for the development of MMP inhibitors. The inhibition of some MMPs could have pro-tumorigenic effects (making them anti-targets), counterbalancing the benefits of target inhibition. These effects might partially account for the failure of MMP inhibitors in clinical trials. What are the major challenges in MMP target validation and MMP-inhibitor-drug development?
Similar articles
-
[Expression of matrix metalloproteinases in patients with malignant tumors].Medicina (Kaunas). 2004;40(12):1143-50. Medicina (Kaunas). 2004. PMID: 15630339 Review. Lithuanian.
-
Matrix metalloproteinase inhibitors and cancer: trials and tribulations.Science. 2002 Mar 29;295(5564):2387-92. doi: 10.1126/science.1067100. Science. 2002. PMID: 11923519 Review.
-
Matrix metalloproteinases. Novel targets for directed cancer therapy.Drugs Aging. 1997 Sep;11(3):229-44. doi: 10.2165/00002512-199711030-00006. Drugs Aging. 1997. PMID: 9303281 Review.
-
Matrix metalloproteinases and cancer - roles in threat and therapy.Asian Pac J Cancer Prev. 2014;15(3):1085-91. doi: 10.7314/apjcp.2014.15.3.1085. Asian Pac J Cancer Prev. 2014. PMID: 24606423 Review.
-
Pigment epithelium-derived factor as a natural matrix metalloproteinase inhibitor: a comparison with classical matrix metalloproteinase inhibitors used for cancer treatment.J Pharm Pharmacol. 2014 Jul;66(7):895-902. doi: 10.1111/jphp.12218. Epub 2014 Feb 12. J Pharm Pharmacol. 2014. PMID: 24697787 Review.
Cited by
-
An MMP13-selective inhibitor delays primary tumor growth and the onset of tumor-associated osteolytic lesions in experimental models of breast cancer.PLoS One. 2012;7(1):e29615. doi: 10.1371/journal.pone.0029615. Epub 2012 Jan 11. PLoS One. 2012. PMID: 22253746 Free PMC article.
-
Analysis of protease activity using quantum dots and resonance energy transfer.Theranostics. 2012;2(2):127-38. doi: 10.7150/thno.3476. Epub 2012 Feb 1. Theranostics. 2012. PMID: 22375154 Free PMC article.
-
How to place the duality of specific MMP-9 inhibition for treatment of inflammatory bowel diseases into clinical opportunities?Front Immunol. 2022 Sep 9;13:983964. doi: 10.3389/fimmu.2022.983964. eCollection 2022. Front Immunol. 2022. PMID: 36164340 Free PMC article. Review.
-
Overexpression of endoglin (CD105) is associated with recurrence in radically resected gastric cancer.Exp Ther Med. 2010 Jul;1(4):627-633. doi: 10.3892/etm_00000098. Epub 2010 Jul 1. Exp Ther Med. 2010. PMID: 22993585 Free PMC article.
-
Genetic variants in matrix metalloproteinase genes as disposition factors for ovarian cancer risk, survival, and clinical outcome.Mol Carcinog. 2015 Jun;54(6):430-9. doi: 10.1002/mc.22111. Epub 2013 Nov 19. Mol Carcinog. 2015. PMID: 25867973 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources