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PMID: 10694567 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Matrix metalloproteinases: biologic activity and clinical implications.

Nelson AR, Fingleton B, Rothenberg ML, Matrisian LM

Abstract

Tumor progression is a complex, multistage process by which a normal cell undergoes genetic changes that result in phenotypic alterations and the acquisition of the ability to spread and colonize distant sites in the body. Although many factors regulate malignant tumor growth and spread, interactions between a tumor and its surrounding microenvironment result in the production of important protein products that are crucial to each step of tumor progression. The matrix metalloproteinases (MMPs) are a family of degradative enzymes with clear links to malignancy. These enzymes are associated with tumor cell invasion of the basement membrane and stroma, blood vessel penetration, and metastasis. They have more recently been implicated in primary and metastatic tumor growth and angiogenesis, and they may even have a role in tumor promotion. This review outlines our current understanding of the MMP family, including the association of particular MMPs with malignant phenotypes and the role of MMPs in specific steps of the metastatic cascade. As scientific understanding of the MMPs has advanced, therapeutic strategies that capitalize on blocking the enzymes have rapidly developed. The preclinical and clinical evolution of the synthetic MMP inhibitors (MMPIs) is also examined, with the discussion encompassing important methodologic issues associated with determining clinical efficacy of MMPIs and other novel therapeutic agents.

MeSH Terms
Animals Antineoplastic Agents/pharmacology,therapeutic use Clinical Trials as Topic Disease Models, Animal Disease Progression Enzyme Inhibitors/pharmacology,therapeutic use Humans Hydroxamic Acids/pharmacology,therapeutic use Matrix Metalloproteinase 1/metabolism Matrix Metalloproteinase Inhibitors Neoplasms/drug therapy,enzymology,metabolism Organic Chemicals
Chemicals
Antineoplastic Agents Enzyme Inhibitors Hydroxamic Acids Matrix Metalloproteinase Inhibitors Organic Chemicals prinomastat marimastat Matrix Metalloproteinase 1
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Nelson A R
Department of Hematology, Vanderbilt University Medical Center, Nashville, TN, USA.
Fingleton B
Rothenberg M L
Matrisian L M
Article Info
Journal
Journal of clinical oncology : official journal of the American Society of Clinical Oncology
Abbr.
J Clin Oncol
ISSN
0732-183X
Published
2000-03-00
Pages
1135-49
Language
English
Region
United States
NLM ID
8309333
Subset
IM
Grants
NCI NIH HHS · R01 CA46843 · United States
NCI NIH HHS · R01 CA60867 · United States
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