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Updated: Jul 18, 2026

Development and Maintenance of a Preclinical Patient Derived Tumor Xenograft Model for the Investigation of Novel Anti-Cancer Therapies
Published on: September 30, 2016
Strategies for MMP inhibition in cancer: innovations for the post-trial era
Christopher Mark Overall1, Carlos López-Otín
1Department of Oral Biological and Medical Sciences, C.I.H.R. Group in Matrix Dynamics, University of British Columbia, V6T 1Z3, Canada.
Abstract:
For more than two decades, the view that tumour-associated matrix metalloproteinases (MMPs) were required for peritumour tissue degradation and metastasis dominated the drive to develop MMP inhibitors as anticancer therapeutics. Until recently, clinical trials with MMP inhibitors have yielded disappointing results, highlighting the need for better insight into the mechanisms by which this growing family of multifunctional enzymes contribute to tumour growth. It is now recognized that MMP activity is tightly regulated at several levels, providing new avenues for blocking these enzymes. What are the different approaches that can be used to target MMPs, and which of these might lead to new therapeutic strategies for cancer?
Insights
Targeting matrix metalloproteinases (MMPs) for cancer therapy has been challenging. New insights into MMP regulation offer novel strategies for developing effective anticancer therapeutics by blocking these enzymes.
Area of Science:
- Biochemistry
- Oncology
- Pharmacology
Background:
- Matrix metalloproteinases (MMPs) have long been implicated in tumor progression and metastasis.
- Previous attempts to develop MMP inhibitors as anticancer drugs yielded disappointing clinical results.
- The complex regulation of MMP activity necessitates a deeper understanding for therapeutic development.
Purpose of the Study:
- To explore diverse strategies for targeting MMPs in cancer.
- To identify promising therapeutic avenues for cancer treatment based on MMP inhibition.
Main Methods:
- Review of existing literature on MMP function and regulation in cancer.
- Analysis of clinical trial outcomes for MMP inhibitors.
- Exploration of novel approaches to modulate MMP activity.
Main Results:
- MMP inhibitors have historically shown limited efficacy in clinical trials.
- MMP activity is subject to intricate multi-level regulation.
- Emerging strategies focus on targeting specific MMPs or their regulatory pathways.
Conclusions:
- Rethinking MMP-targeted cancer therapy is crucial.
- Understanding MMP regulation provides new opportunities for drug development.
- Targeting MMPs offers potential for novel anticancer strategies.
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