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Survivin (BIRC5) Gene Polymorphism (rs9904341) Is Associated with Cancer Risk: A Meta-Analysis.
Neha Malviya1, Anam Khan2, Ananyan Sampath2
1Department of Biotechnology, Institute for Excellence in Higher Education, Bhopal, India.
The survivin (BIRC5) -31G/C gene polymorphism (rs9904341) is linked to increased cancer risk, particularly in Asian populations. Further research is needed to confirm these findings.
Area of Science:
- Genetics
- Oncology
- Molecular Biology
Background:
- Survivin (BIRC5) is an anti-apoptotic protein frequently overexpressed in various cancers.
- Elevated survivin levels correlate with adverse clinical outcomes in cancer patients.
- The -31G/C (rs9904341) polymorphism in the BIRC5 gene has been investigated for its association with cancer susceptibility.
Purpose of the Study:
- To conduct an updated meta-analysis evaluating the association between the survivin -31G/C (rs9904341) gene polymorphism and overall cancer risk.
- To assess the impact of this polymorphism across different genetic models and in specific ethnic groups.
Main Methods:
- A comprehensive literature search was performed using PubMed and Google Scholar.
- Data from 51 studies, including 10472 cases and 12193 controls, were pooled for meta-analysis.
- Statistical analyses, including sensitivity and risk of bias assessments, were conducted using RevMan 5.4 and Excel 2013.
Main Results:
- The meta-analysis revealed a significant association between the survivin -31G/C polymorphism and overall cancer risk across multiple genetic models (allelic, co-dominant, dominant, and recessive).
- Specifically, the C allele and CC genotype were associated with increased cancer risk.
- Stratified analysis indicated a significantly higher risk in the Asian population.
Conclusions:
- The -31G/C (rs9904341) polymorphism of the BIRC5 gene is associated with cancer risk, particularly in the Asian population.
- These findings highlight the potential role of this genetic variant in cancer susceptibility.
- Larger-scale clinical studies are recommended for further validation.
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