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Targeting Invasion: The Role of MMP-2 and MMP-9 Inhibition in Colorectal Cancer Therapy
Alireza Shoari1, Arghavan Ashja Ardalan2, Alexandra M Dimesa1
1Department of Cancer Biology, Mayo Clinic, Jacksonville, FL 32224, USA.
Abstract:
Colorectal cancer (CRC) remains one of the most prevalent and lethal cancers worldwide, prompting ongoing research into innovative therapeutic strategies. This review aims to systematically evaluate the role of gelatinases, specifically MMP-2 and MMP-9, as therapeutic targets in CRC, providing a critical analysis of their potential to improve patient outcomes. Gelatinases, specifically MMP-2 and MMP-9, play critical roles in the processes of tumor growth, invasion, and metastasis. Their expression and activity are significantly elevated in CRC, correlating with poor prognosis and lower survival rates. This review provides a comprehensive overview of the pathophysiological roles of gelatinases in CRC, highlighting their contribution to tumor microenvironment modulation, angiogenesis, and the metastatic cascade. We also critically evaluate recent advancements in the development of gelatinase inhibitors, including small molecule inhibitors, natural compounds, and novel therapeutic approaches like gene silencing techniques. Challenges such as nonspecificity, adverse side effects, and resistance mechanisms are discussed. We explore the potential of gelatinase inhibition in combination therapies, particularly with conventional chemotherapy and emerging targeted treatments, to enhance therapeutic efficacy and overcome resistance. The novelty of this review lies in its integration of recent findings on diverse inhibition strategies with insights into their clinical relevance, offering a roadmap for future research. By addressing the limitations of current approaches and proposing novel strategies, this review underscores the potential of gelatinase inhibitors in CRC prevention and therapy, inspiring further exploration in this promising area of oncological treatment.
Insights
Gelatinases (MMP-2 and MMP-9) are key drivers of colorectal cancer (CRC) progression. Inhibiting these enzymes shows promise for new CRC therapies and improving patient outcomes.
Area of Science:
- Oncology
- Biochemistry
Background:
- Colorectal cancer (CRC) is a leading cause of cancer-related deaths globally.
- Gelatinases, specifically matrix metalloproteinases-2 (MMP-2) and -9 (MMP-9), are implicated in CRC progression, invasion, and metastasis.
- Elevated MMP-2 and MMP-9 expression in CRC correlates with poor prognosis.
Purpose of the Study:
- To systematically review the role of MMP-2 and MMP-9 as therapeutic targets in CRC.
- To critically analyze the potential of gelatinase inhibitors to improve patient outcomes.
- To explore novel therapeutic strategies and combination therapies involving gelatinase inhibition.
Main Methods:
- Comprehensive literature review of pathophysiological roles of gelatinases in CRC.
- Evaluation of recent advancements in MMP-2 and MMP-9 inhibitor development.
- Analysis of challenges, resistance mechanisms, and clinical relevance of inhibition strategies.
Main Results:
- MMP-2 and MMP-9 significantly contribute to CRC tumor microenvironment modulation, angiogenesis, and metastasis.
- Various inhibitors, including small molecules, natural compounds, and gene silencing techniques, are under development.
- Combination therapies with chemotherapy and targeted treatments show potential to enhance efficacy.
Conclusions:
- Gelatinase inhibition presents a promising therapeutic avenue for CRC prevention and treatment.
- Addressing challenges like specificity and resistance is crucial for clinical translation.
- Further research into novel inhibition strategies and combination therapies is warranted.
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