Matrix metalloproteinases in colorectal cancer: is it worth talking about?

Matrix metalloproteinases (MMPs), a family of extracellular matrix degrading enzymes, are expressed in various stages of colorectal cancer (CRC) and correlate with survival and prognosis. There is considerable evidence in preclinical models that MMP inhibitors (MMPIs) are effective at multiple stage...

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Veröffentlicht in:Cancer and metastasis reviews 2004-01, Vol.23 (1-2), p.119-135
Hauptverfasser: Wagenaar-Miller, Rebecca A, Gorden, Lee, Matrisian, Lynn M
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Gorden, Lee
Matrisian, Lynn M
description Matrix metalloproteinases (MMPs), a family of extracellular matrix degrading enzymes, are expressed in various stages of colorectal cancer (CRC) and correlate with survival and prognosis. There is considerable evidence in preclinical models that MMP inhibitors (MMPIs) are effective at multiple stages of CRC tumor progression, including reducing the number of intestinal adenomas, inhibiting the growth and establishment of primary CRC tumors, and reducing metastasis to the lung and liver. However, clinical trials with MMPIs in other tumor types have been largely unsuccessful, raising the question as to whether MMPs represent therapeutic targets in CRC. This review focuses on the expression, role, and contribution of MMP family members to various stages of CRC tumor progression. The conclusion is that there is considerable evidence to suggest that MMP inhibition may be an effective strategy if applied at either end of the tumor progression spectrum; the prevention of adenomas, or the treatment of micrometastatic disease.
doi_str_mv 10.1023/A:1025819214508
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subjects Adenoma - metabolism
Clinical Trials as Topic
Colorectal cancer
Colorectal Neoplasms - enzymology
Disease Progression
Humans
Intestinal Diseases - metabolism
Matrix Metalloproteinases - metabolism
Matrix Metalloproteinases - physiology
Models, Biological
Neoplasm Metastasis
Prognosis
Protein Structure, Tertiary
title Matrix metalloproteinases in colorectal cancer: is it worth talking about?
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