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MTHFR polymorphism and the risk of prostate cancer: a meta-analysis of case-control studies
1Department of Nutrition and Food Hygiene, School of Public Health, Medical College of Soochow University, Suzhou, Jiangsu, China. lixinli@suda.edu.cn
Background:
5,10-Methylenetetrahydrofolate reductase (MTHFR) polymorphisms implicated in the cancer development, but the published studies had yielded inconsistent results.
Methods:
Pubmed was searched for all published case-control studies about MTHFR polymorphisms and prostate cancer risk.
Results:
In all, 13 studies including 5872 cases and 6255 controls described C677T genotypes, among which 9 articles, containing 2847 cases and 3657 controls described A1298C genotypes, were involved in our meta-analysis. Odds ratios (ORs) with 95% confidence intervals (CIs) were estimated to assess the association between MTHFR polymorphisms and prostate cancer risk, heterogeneity, publication bias and sensitivity were also calculated. Overall, meta-analysis indicated that the 677T allele was more likely to exert protective effect on prostate cancer risk (random-effects pooled OR, 0.78 (0.64-0.96); P=0.016 (P=0.033 for heterogeneity studies)) in a recessive genetic model, no associations were found in other genetic models or in comparing a/a versus A/A homozygous. Neither did we find any difference in effects on high or low aggressive prostate cancer. No evidence of an association of MTHFR A1298C polymorphism with prostate cancer was found.
Conclusions:
C677T of the MTHFR gene may provide protective effects on susceptibility to prostate cancer risk.
Insights
The 5,10-Methylenetetrahydrofolate reductase (MTHFR) C677T gene variant may reduce prostate cancer risk. This meta-analysis found a protective effect, particularly in a recessive genetic model, for the 677T allele.
Area of Science:
- Genetics
- Oncology
- Nutritional Biochemistry
Background:
- 5,10-Methylenetetrahydrofolate reductase (MTHFR) gene polymorphisms are linked to cancer development.
- Previous studies on MTHFR and prostate cancer risk have shown conflicting results.
Purpose of the Study:
- To conduct a meta-analysis of case-control studies to investigate the association between MTHFR gene polymorphisms and prostate cancer risk.
- To clarify the inconsistent findings regarding MTHFR polymorphisms and their role in prostate cancer susceptibility.
Main Methods:
- A comprehensive literature search was performed on PubMed for relevant case-control studies.
- Meta-analysis was used to pool data on MTHFR C677T and A1298C genotypes, calculating odds ratios (ORs) with 95% confidence intervals (CIs).
- Heterogeneity, publication bias, and sensitivity analyses were conducted to ensure the robustness of the findings.
Main Results:
- The meta-analysis included 13 studies for MTHFR C677T (5872 cases, 6255 controls) and 9 studies for A1298C (2847 cases, 3657 controls).
- The 677T allele showed a protective effect against prostate cancer risk in a recessive genetic model (pooled OR, 0.78; P=0.016).
- No significant associations were found for other genetic models of C677T, the A1298C polymorphism, or in relation to prostate cancer aggressiveness.
Conclusions:
- The C677T polymorphism in the MTHFR gene may offer a protective effect against prostate cancer susceptibility.
- The MTHFR A1298C polymorphism was not found to be associated with prostate cancer risk.
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