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PMID: 16498445 Published · ppublish English Research Support, Non-U.S. Gov't Review

Tumour microenvironment - opinion: validating matrix metalloproteinases as drug targets and anti-targets for cancer therapy.

Nature reviews. Cancer ·Vol. 6 ·No. 3 ·2006-00-00 ·Pages 227-39

Overall CM, Kleifeld O

Abstract

The matrix metalloproteinases (MMPs) mediate homeostasis of the extracellular environment. They have multiple signalling activities that are commonly altered during tumorigenesis and that might serve as intervention points for anticancer drugs. However, there are many criteria to consider in validating MMPs as drug targets and for the development of MMP inhibitors. The inhibition of some MMPs could have pro-tumorigenic effects (making them anti-targets), counterbalancing the benefits of target inhibition. These effects might partially account for the failure of MMP inhibitors in clinical trials. What are the major challenges in MMP target validation and MMP-inhibitor-drug development?

MeSH Terms
Antineoplastic Agents/therapeutic use Cell Transformation, Neoplastic Extracellular Matrix/metabolism Forecasting Gene Expression Regulation, Enzymologic Matrix Metalloproteinase Inhibitors Matrix Metalloproteinases/classification,metabolism Neoplasm Invasiveness Neoplasms/drug therapy,enzymology Neovascularization, Pathologic Protease Inhibitors/therapeutic use Tissue Inhibitor of Metalloproteinases/therapeutic use
Chemicals
Antineoplastic Agents Matrix Metalloproteinase Inhibitors Protease Inhibitors Tissue Inhibitor of Metalloproteinases Matrix Metalloproteinases
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Overall Christopher M
University of British Columbia Centre for Blood Research, CBCRA Program in Breast Cancer Metastasis, Department of Oral Biological & Medical Sciences, University of British Columbia, Vancouver, British Columbia, Canada V6T 1Z3. chris.overall@ubc.ca
Kleifeld Oded
Article Info
Journal
Nature reviews. Cancer
Abbr.
Nat Rev Cancer
ISSN
1474-175X
Published
2006-00-00
Pages
227-39
Language
English
Region
England
NLM ID
101124168
Subset
IM
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