Matrix metalloproteinase inhibitors and cancer: trials and tribulations - PubMed (original) (raw)
Review
. 2002 Mar 29;295(5564):2387-92.
doi: 10.1126/science.1067100.
Affiliations
- PMID: 11923519
- DOI: 10.1126/science.1067100
Review
Matrix metalloproteinase inhibitors and cancer: trials and tribulations
Lisa M Coussens et al. Science. 2002.
Abstract
For at least 30 years, matrix metalloproteinases (MMPs) have been heralded as promising targets for cancer therapy on the basis of their massive up-regulation in malignant tissues and their unique ability to degrade all components of the extracellular matrix. Preclinical studies testing the efficacy of MMP suppression in tumor models were so compelling that synthetic metalloproteinase inhibitors (MPIs) were rapidly developed and routed into human clinical trials. The results of these trials have been disappointing. Here we review the studies that brought MPIs into clinical testing and discuss the design and outcome of the trials in light of new information about the cellular source, substrates, and mode of action of MMPs at different stages of tumor progression. The important lessons learned from the MPI experience may be of great value for future studies of MPIs and for cancer drug development in general.
Similar articles
- Matrix metalloproteinase inhibitors.
Ramnath N, Creaven PJ. Ramnath N, et al. Curr Oncol Rep. 2004 Mar;6(2):96-102. doi: 10.1007/s11912-004-0020-7. Curr Oncol Rep. 2004. PMID: 14751086 Review. - Tumour microenvironment - opinion: validating matrix metalloproteinases as drug targets and anti-targets for cancer therapy.
Overall CM, Kleifeld O. Overall CM, et al. Nat Rev Cancer. 2006 Mar;6(3):227-39. doi: 10.1038/nrc1821. Nat Rev Cancer. 2006. PMID: 16498445 Review. - Natural bio-drugs as matrix metalloproteinase inhibitors: new perspectives on the horizon?
Mannello F. Mannello F. Recent Pat Anticancer Drug Discov. 2006 Jan;1(1):91-103. doi: 10.2174/157489206775246421. Recent Pat Anticancer Drug Discov. 2006. PMID: 18221029 Review. - Matrix metalloproteinase inhibitors.
Wojtowicz-Praga SM, Dickson RB, Hawkins MJ. Wojtowicz-Praga SM, et al. Invest New Drugs. 1997;15(1):61-75. doi: 10.1023/a:1005722729132. Invest New Drugs. 1997. PMID: 9195290 Review. - Progress in the development of matrix metalloproteinase inhibitors.
Tu G, Xu W, Huang H, Li S. Tu G, et al. Curr Med Chem. 2008;15(14):1388-95. doi: 10.2174/092986708784567680. Curr Med Chem. 2008. PMID: 18537616 Review.
Cited by
- Silencing of diphthamide synthesis 3 (Dph3) reduces metastasis of murine melanoma.
Wang L, Shi Y, Ju P, Liu R, Yeo SP, Xia Y, Owlanj H, Feng Z. Wang L, et al. PLoS One. 2012;7(11):e49988. doi: 10.1371/journal.pone.0049988. Epub 2012 Nov 20. PLoS One. 2012. PMID: 23185508 Free PMC article. - p53 regulates cytoskeleton remodeling to suppress tumor progression.
Araki K, Ebata T, Guo AK, Tobiume K, Wolf SJ, Kawauchi K. Araki K, et al. Cell Mol Life Sci. 2015 Nov;72(21):4077-94. doi: 10.1007/s00018-015-1989-9. Epub 2015 Jul 24. Cell Mol Life Sci. 2015. PMID: 26206378 Free PMC article. Review. - Molecular evaluation of chronic restrain stress in mice model of non metastatic fibrosarcoma.
Smieško G, Banović P, Gusman V, Simin V, Cimpean AM, Lalošević D. Smieško G, et al. J Mol Histol. 2020 Aug;51(4):367-374. doi: 10.1007/s10735-020-09886-5. Epub 2020 Jun 15. J Mol Histol. 2020. PMID: 32556790 - Matrix metalloproteinase-13 is regulated by toll-like receptor-9 in colorectal cancer cells and mediates cellular migration.
Rath T, Stöckle J, Roderfeld M, Tschuschner A, Graf J, Roeb E. Rath T, et al. Oncol Lett. 2011 May;2(3):483-488. doi: 10.3892/ol.2011.276. Epub 2011 Mar 21. Oncol Lett. 2011. PMID: 22866107 Free PMC article. - Functional cooperativity by direct interaction between PAK4 and MMP-2 in the regulation of anoikis resistance, migration and invasion in glioma.
Kesanakurti D, Chetty C, Rajasekhar Maddirela D, Gujrati M, Rao JS. Kesanakurti D, et al. Cell Death Dis. 2012 Dec 20;3(12):e445. doi: 10.1038/cddis.2012.182. Cell Death Dis. 2012. PMID: 23254288 Free PMC article.
Publication types
MeSH terms
Substances
Grants and funding
- CA72006/CA/NCI NIH HHS/United States
- P30CA68485/CA/NCI NIH HHS/United States
- P50CA90949/CA/NCI NIH HHS/United States
- R01CA60867/CA/NCI NIH HHS/United States
- R01CA84360/CA/NCI NIH HHS/United States
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical