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Metalloproteinases: role in breast carcinogenesis, invasion and metastasis
The matrix metalloproteinases (MMPs) are a family of zinc-dependent endopeptidases. Their primary function is degradation of proteins in the extracellular matrix. Currently, at least 19 members of this family are known to exist. Based on substrate specificity and domain organization, the MMPs can be...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2000
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC138784/ https://www.ncbi.nlm.nih.gov/pubmed/11250717 http://dx.doi.org/10.1186/bcr65 |
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author | Duffy, Michael J Maguire, Teresa M Hill, Arnold McDermott, Enda O'Higgins, Niall |
author_facet | Duffy, Michael J Maguire, Teresa M Hill, Arnold McDermott, Enda O'Higgins, Niall |
author_sort | Duffy, Michael J |
collection | PubMed |
description | The matrix metalloproteinases (MMPs) are a family of zinc-dependent endopeptidases. Their primary function is degradation of proteins in the extracellular matrix. Currently, at least 19 members of this family are known to exist. Based on substrate specificity and domain organization, the MMPs can be loosely divided into four main groups: the interstitial collagenases, gelatinases, stromelysins and membrane-type MMPs. Recent data from model systems suggest that MMPs are involved in breast cancer initiation, invasion and metastasis. Consistent with their role in breast cancer progression, high levels of at least two MMPs (MMP-2 and stromelysin-3) have been found to correlate with poor prognosis in patients with breast cancer. Because MMPs are apparently involved in breast cancer initiation and dissemination, inhibition of these proteinases may be of value both in preventing breast cancer and in blocking metastasis of established tumours |
format | Text |
id | pubmed-138784 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2000 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-1387842003-02-27 Metalloproteinases: role in breast carcinogenesis, invasion and metastasis Duffy, Michael J Maguire, Teresa M Hill, Arnold McDermott, Enda O'Higgins, Niall Breast Cancer Res Review The matrix metalloproteinases (MMPs) are a family of zinc-dependent endopeptidases. Their primary function is degradation of proteins in the extracellular matrix. Currently, at least 19 members of this family are known to exist. Based on substrate specificity and domain organization, the MMPs can be loosely divided into four main groups: the interstitial collagenases, gelatinases, stromelysins and membrane-type MMPs. Recent data from model systems suggest that MMPs are involved in breast cancer initiation, invasion and metastasis. Consistent with their role in breast cancer progression, high levels of at least two MMPs (MMP-2 and stromelysin-3) have been found to correlate with poor prognosis in patients with breast cancer. Because MMPs are apparently involved in breast cancer initiation and dissemination, inhibition of these proteinases may be of value both in preventing breast cancer and in blocking metastasis of established tumours BioMed Central 2000 2000-06-07 /pmc/articles/PMC138784/ /pubmed/11250717 http://dx.doi.org/10.1186/bcr65 Text en Copyright © 2000 Current Science Ltd |
spellingShingle | Review Duffy, Michael J Maguire, Teresa M Hill, Arnold McDermott, Enda O'Higgins, Niall Metalloproteinases: role in breast carcinogenesis, invasion and metastasis |
title | Metalloproteinases: role in breast carcinogenesis, invasion and metastasis |
title_full | Metalloproteinases: role in breast carcinogenesis, invasion and metastasis |
title_fullStr | Metalloproteinases: role in breast carcinogenesis, invasion and metastasis |
title_full_unstemmed | Metalloproteinases: role in breast carcinogenesis, invasion and metastasis |
title_short | Metalloproteinases: role in breast carcinogenesis, invasion and metastasis |
title_sort | metalloproteinases: role in breast carcinogenesis, invasion and metastasis |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC138784/ https://www.ncbi.nlm.nih.gov/pubmed/11250717 http://dx.doi.org/10.1186/bcr65 |
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