Literature DB >> 7764458

Role of matrix metalloproteinases in invasion and metastasis: biology, diagnosis and inhibitors.

S McDonnell1, B Fingleton.   

Abstract

The processes of tumour invasion and subsequent metastasis are the most lethal aspects of cancer. Whilst many factors are involved, the matrix metalloproteinases (MMPs) have been implicated as key-rate limiting enzymes in the invasive process. This family consisting of eight members of similar structure, can be roughly divided into three groups based on substrate specificity. All are secreted in a latent form and require proteolytic cleavage for activation. The expression of these enzymes is regulated at the transcriptional level by a variety of growth factors and oncogenes. They are also regulated at the protein level by a family of specific inhibitors called the tissue inhibitors of metalloproteinases (TIMPs). Studies in human tumour samples have shown a positive correlation between metalloproteinase expression and metastatic potential. The levels of metalloproteinase expression have been manipulated using molecular biology techniques in several cell lines and shown a similar correlation. These results suggest that an understanding of metalloproteinase expression and proteolytic activity may lead to the development of effective therapeutic agents with the potential to reduce the incidence of metastatic cancer.

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Year:  1993        PMID: 7764458     DOI: 10.1007/BF00744674

Source DB:  PubMed          Journal:  Cytotechnology        ISSN: 0920-9069            Impact factor:   2.058


  107 in total

1.  The complex between a tissue inhibitor of metalloproteinases (TIMP-2) and 72-kDa progelatinase is a metalloproteinase inhibitor.

Authors:  H Kolkenbrock; D Orgel; A Hecker-Kia; W Noack; N Ulbrich
Journal:  Eur J Biochem       Date:  1991-06-15

2.  Epidermal growth factor stimulation of stromelysin mRNA in rat fibroblasts requires induction of proto-oncogenes c-fos and c-jun and activation of protein kinase C.

Authors:  S E McDonnell; L D Kerr; L M Matrisian
Journal:  Mol Cell Biol       Date:  1990-08       Impact factor: 4.272

Review 3.  Stromelysin in tumor progression and metastasis.

Authors:  S McDonnell; L M Matrisian
Journal:  Cancer Metastasis Rev       Date:  1990-12       Impact factor: 9.264

4.  Reduced tumor incidence, metastatic potential, and cytokine responsiveness of nm23-transfected melanoma cells.

Authors:  A Leone; U Flatow; C R King; M A Sandeen; I M Margulies; L A Liotta; P S Steeg
Journal:  Cell       Date:  1991-04-05       Impact factor: 41.582

5.  Prolonged activation of jun and collagenase genes by tumour necrosis factor-alpha.

Authors:  D A Brenner; M O'Hara; P Angel; M Chojkier; M Karin
Journal:  Nature       Date:  1989-02-16       Impact factor: 49.962

6.  Immunohistochemical distribution of type IV collagenase in normal, benign, and malignant breast tissue.

Authors:  C Monteagudo; M J Merino; J San-Juan; L A Liotta; W G Stetler-Stevenson
Journal:  Am J Pathol       Date:  1990-03       Impact factor: 4.307

7.  Association of nm23-H1 allelic deletions with distant metastases in colorectal carcinoma.

Authors:  K H Cohn; F S Wang; F Desoto-LaPaix; W B Solomon; L G Patterson; M R Arnold; J Weimar; J G Feldman; A T Levy; A Leone
Journal:  Lancet       Date:  1991-09-21       Impact factor: 79.321

8.  Human neutrophil collagenase. A distinct gene product with homology to other matrix metalloproteinases.

Authors:  K A Hasty; T F Pourmotabbed; G I Goldberg; J P Thompson; D G Spinella; R M Stevens; C L Mainardi
Journal:  J Biol Chem       Date:  1990-07-15       Impact factor: 5.157

9.  Human 72-kilodalton type IV collagenase forms a complex with a tissue inhibitor of metalloproteases designated TIMP-2.

Authors:  G I Goldberg; B L Marmer; G A Grant; A Z Eisen; S Wilhelm; C S He
Journal:  Proc Natl Acad Sci U S A       Date:  1989-11       Impact factor: 11.205

10.  Human skin fibroblast stromelysin: structure, glycosylation, substrate specificity, and differential expression in normal and tumorigenic cells.

Authors:  S M Wilhelm; I E Collier; A Kronberger; A Z Eisen; B L Marmer; G A Grant; E A Bauer; G I Goldberg
Journal:  Proc Natl Acad Sci U S A       Date:  1987-10       Impact factor: 11.205

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  3 in total

1.  Quercetin downregulates matrix metalloproteinases 2 and 9 proteins expression in prostate cancer cells (PC-3).

Authors:  M R Vijayababu; A Arunkumar; P Kanagaraj; P Venkataraman; G Krishnamoorthy; J Arunakaran
Journal:  Mol Cell Biochem       Date:  2006-04-28       Impact factor: 3.396

2.  Metastatic and non-metastatic colorectal cancer (CRC) cells induce host metalloproteinase production in vivo.

Authors:  S Mc Donnell; V Chaudhry; J Mansilla-Soto; Z S Zeng; W P Shu; J G Guillem
Journal:  Clin Exp Metastasis       Date:  1999-06       Impact factor: 5.150

3.  Effects of luteolin and quercetin, inhibitors of tyrosine kinase, on cell growth and metastasis-associated properties in A431 cells overexpressing epidermal growth factor receptor.

Authors:  Y T Huang; J J Hwang; P P Lee; F C Ke; J H Huang; C J Huang; C Kandaswami; E Middleton; M T Lee
Journal:  Br J Pharmacol       Date:  1999-11       Impact factor: 8.739

  3 in total

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