Overview of matrix metalloproteinase expression in cultured human cells
- PMID: 9550265
- DOI: 10.1016/s0945-053x(98)90019-1
Overview of matrix metalloproteinase expression in cultured human cells
Abstract
The matrix metalloproteinases (MMP) have been implicated in tumor invasion and metastasis both by immunohistochemical studies and from the observation that specific metalloproteinase inhibitors block tumor invasion and metastasis. Oligonucleotide primers for thirteen MMPs (MMP-1, MMP-2, MMP-3, MMP-7, MMP-8, MMP-9, MMP-10, MMP-11, MMP-12, MMP-13, MMP-14, MMP-15, MMP-16) were optimized for use in RT-PCR. A semi-quantitative RT-PCR assay was used to determine the pattern of MMP mRNA expression in 84 normal and transformed or carcinogen transformed human cell lines and strains derived from different tissues. The results demonstrate one or more cell lines which express thirteen members of the MMP family. In addition, various oncogene transfected human fibroblast cell strains were analyzed for MMP expression. We confirm that over-expression of the H-ras oncoprotein correlates with up-regulation of MMP-9 and demonstrate that over-expression of v-sis also up-regulates MMP-9. A cell line immortalized following myc expression was found to up-regulate MMP-7, MMP-11 and MMP-13. Inappropriate expression of several MMP mRNAs was detected in breast, prostate, bone, colon and oral tumor derived cell lines. Identification of at least one cell line expressing each of thirteen MMPs and the observation of oncogene induced expression of several MMPs should facilitate analysis of the transcriptional mechanisms controlling each MMP.
Similar articles
-
Role of the matrix metalloproteinase and tissue inhibitors of metalloproteinase families in noninvasive and invasive tumors transplanted in mice with severe combined immunodeficiency.Urology. 1998 May;51(5):849-53. doi: 10.1016/s0090-4295(98)00010-7. Urology. 1998. PMID: 9610608
-
Differential expression of matrix metalloproteinases in activated c-ras-Ha-transfected immortalized human keratinocytes.Br J Cancer. 1998 Mar;77(5):724-30. doi: 10.1038/bjc.1998.119. Br J Cancer. 1998. PMID: 9514050 Free PMC article.
-
Expression and tissue localization of membrane-types 1, 2, and 3 matrix metalloproteinases in human urothelial carcinomas.J Urol. 1998 Oct;160(4):1540-5. J Urol. 1998. PMID: 9751409
-
RECK: a novel suppressor of malignancy linking oncogenic signaling to extracellular matrix remodeling.Cancer Metastasis Rev. 2003 Jun-Sep;22(2-3):167-75. doi: 10.1023/a:1023043315031. Cancer Metastasis Rev. 2003. PMID: 12784995 Review.
-
Polymorphism in matrix metalloproteinase gene promoters: implication in regulation of gene expression and susceptibility of various diseases.Matrix Biol. 2000 Dec;19(7):623-9. doi: 10.1016/s0945-053x(00)00102-5. Matrix Biol. 2000. PMID: 11102751 Review.
Cited by
-
Modular GAG-matrices to promote mammary epithelial morphogenesis in vitro.Biomaterials. 2017 Jan;112:20-30. doi: 10.1016/j.biomaterials.2016.10.007. Epub 2016 Oct 6. Biomaterials. 2017. PMID: 27741500 Free PMC article.
-
Development of a novel fluorogenic proteolytic beacon for in vivo detection and imaging of tumour-associated matrix metalloproteinase-7 activity.Biochem J. 2004 Feb 1;377(Pt 3):617-28. doi: 10.1042/BJ20030582. Biochem J. 2004. PMID: 14556651 Free PMC article.
-
Dentin matrix protein 1 enhances invasion potential of colon cancer cells by bridging matrix metalloproteinase-9 to integrins and CD44.Cancer Res. 2005 Dec 15;65(24):11545-52. doi: 10.1158/0008-5472.CAN-05-2861. Cancer Res. 2005. PMID: 16357164 Free PMC article.
-
Stimuli-responsive nanoparticles for targeting the tumor microenvironment.J Control Release. 2015 Dec 10;219:205-214. doi: 10.1016/j.jconrel.2015.08.050. Epub 2015 Sep 1. J Control Release. 2015. PMID: 26341694 Free PMC article. Review.
-
ING2 is upregulated in colon cancer and increases invasion by enhanced MMP13 expression.Int J Cancer. 2009 Sep 15;125(6):1306-15. doi: 10.1002/ijc.24437. Int J Cancer. 2009. PMID: 19437536 Free PMC article.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Research Materials
Miscellaneous