Abstract |
Hematogenous metastasis is postulated to involve tumor cell-initiated degradation of basement membrane barriers and underlying connective tissue matrices. Matrix metalloproteinases ( MMP) are zinc-dependent endopeptidases that have been implicated in the proteolytic events of tumor cell invasion. Research has revealed a class of membrane-anchored metalloproteinases (MT- MMPs) and has provided convincing evidence that these enzymes activate latent MMP-2 ( 72 kDa gelatinase A) on the cell surface. The activation of plasma membrane associated MMP is a potential mechanism for facilitation of cellular metastasis and requires consideration when addressing potential roles of MMPs in tumor progression. This review focuses on potential in vivo regulatory mechanisms of membrane-associated MMP activity in the context of tumor cell interaction with matrix macromolecules. BioEssays 1999;21:940-949.
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Authors | S M Ellerbroek, M S Stack |
Journal | BioEssays : news and reviews in molecular, cellular and developmental biology
(Bioessays)
Vol. 21
Issue 11
Pg. 940-9
(Nov 1999)
ISSN: 0265-9247 [Print] United States |
PMID | 10517867
(Publication Type: Journal Article, Research Support, U.S. Gov't, P.H.S., Review)
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Copyright | Copyright 1999 John Wiley & Sons, Inc. |
Chemical References |
- Metalloendopeptidases
- Matrix Metalloproteinase 2
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Topics |
- Basement Membrane
(metabolism)
- Cell Membrane
(enzymology)
- Connective Tissue
(metabolism)
- Enzyme Activation
- Extracellular Matrix
(metabolism)
- Gene Expression Regulation, Neoplastic
- Humans
- Matrix Metalloproteinase 2
(metabolism)
- Metalloendopeptidases
(chemistry)
- Neoplasm Metastasis
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