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Updated: Feb 16, 2026

miRNA Expression Analyses in Prostate Cancer Clinical Tissues
Published on: September 8, 2015
Genetic Association between Matrix Metalloproteinases Gene Polymorphisms and Risk of Prostate Cancer: A Meta-Analysis
Hong Weng1,2, Xian-Tao Zeng1,2, Xing-Huan Wang1,2
1Department of Urology, Zhongnan Hospital of Wuhan University, Wuhan, China.
Abstract:
Background and Objective: Studies suggests that matrix metalloproteinase (MMP)-2-1306 C/T and MMP-1-1607 1G/2G polymorphisms affect the risk of prostate cancer. However, the conclusions remain controversial and no pooled evidence of this topic has been published. Therefore, we aimed to perform a meta-analysis to shed some light on the controversial conclusion pertaining to the associations of MMP-2-1306 C/T and MMP-1-1607 1G/2G polymorphisms with prostate cancer susceptibility. Methods: A thorough literature search was performed up to August, 2016 with the PubMed, EMBASE, CBM, CNKI, and Wanfang databases. Odds ratios (ORs) and corresponding 95% confidence intervals (95% CIs) were calculated to address the correlations between these polymorphisms and risk of prostate cancer. Results: The meta-analysis included six studies (1,921 patients and 1,988 controls) on MMP-2-1306 C/T polymorphism and three studies on MMP-1-1607 1G/2G polymorphism (438 patients and 394 controls), respectively. The overall results of meta-analysis showed that an elevated risk of the disease was implicated in MMP-2-1306 C/T polymorphism under two genetic models (CT vs. CC: OR = 1.78, 95% CI = 1.33-2.38; TT+CT vs. CC: OR = 1.62, 95% CI = 1.24-2.12) and no significant association was observed between MMP-1-1607 1G/2G polymorphism and the risk of prostate cancer. The subgroup analysis results of MMP-2-1306 C/T polymorphism were similar to the overall results. However, decreased risk of prostate cancer was observed in the Caucasians for MMP-1-1607 1G/2G polymorphism. Conclusions: Current meta-analysis indicates that MMP-2-1306 C/T polymorphism is associated with elevated risk of prostate cancer, but MMP-1-1607 1G/2G polymorphism may inhibit the occurrence of prostate cancer in Caucasians. Further studies are warranted to verify the conclusions.
Insights
This meta-analysis found that the matrix metalloproteinase (MMP)-2-1306 C/T polymorphism increases prostate cancer risk. The MMP-1-1607 1G/2G polymorphism may decrease risk in Caucasians.
Area of Science:
- Genetics
- Oncology
- Molecular Biology
Background:
- Prostate cancer risk may be influenced by matrix metalloproteinase (MMP)-2-1306 C/T and MMP-1-1607 1G/2G gene polymorphisms.
- Previous studies have yielded controversial results, lacking pooled evidence on these associations.
Purpose of the Study:
- To conduct a meta-analysis investigating the association between MMP-2-1306 C/T and MMP-1-1607 1G/2G polymorphisms and prostate cancer susceptibility.
- To provide pooled evidence to clarify controversial findings in the existing literature.
Main Methods:
- A comprehensive literature search was conducted across multiple databases (PubMed, EMBASE, CBM, CNKI, Wanfang) up to August 2016.
- Odds ratios (ORs) and 95% confidence intervals (95% CIs) were calculated to assess the correlation between polymorphisms and prostate cancer risk.
Main Results:
- The meta-analysis included six studies for MMP-2-1306 C/T (1,921 cases, 1,988 controls) and three studies for MMP-1-1607 1G/2G (438 cases, 394 controls).
- MMP-2-1306 C/T polymorphism was associated with an elevated risk of prostate cancer (CT vs. CC: OR=1.78; TT+CT vs. CC: OR=1.62).
- No significant association was found for MMP-1-1607 1G/2G, although a decreased risk was observed in Caucasians.
Conclusions:
- The MMP-2-1306 C/T polymorphism is linked to an increased risk of developing prostate cancer.
- The MMP-1-1607 1G/2G polymorphism might play an inhibitory role in prostate cancer occurrence among Caucasians.
- Further research is recommended to validate these findings.
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