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Published on: September 25, 2013
Association of hOGG1 Ser326Cys polymorphism with susceptibility to hepatocellular carcinoma
1Department of Clinical Laboratory, Renmin Hospital of Wuhan University Wuhan 430060, Hubei, China.
Insights
The hOGG1 Ser326Cys polymorphism is linked to a higher risk of developing hepatocellular carcinoma (HCC). This meta-analysis confirms a significant association between this genetic variation and increased susceptibility to HCC.
Area of Science:
- Genetics and Genomics
- Cancer Research
- Molecular Epidemiology
Background:
- The association between the hOGG1 Ser326Cys polymorphism and hepatocellular carcinoma (HCC) risk has yielded inconsistent findings in previous studies.
- This meta-analysis aims to provide a more precise estimation of this relationship by synthesizing existing evidence.
Purpose of the Study:
- To evaluate the association between the hOGG1 Ser326Cys polymorphism and the risk of developing HCC.
- To clarify the conflicting results reported in the literature regarding this genetic polymorphism and HCC susceptibility.
Main Methods:
- A comprehensive literature search was conducted across PubMed, CBM, and EMBASE databases.
- Nine case-control studies, including 2583 HCC patients and 2271 controls, were included in this meta-analysis.
- Pooled odds ratios (ORs) and 95% confidence intervals (CIs) were calculated using fixed-effect or random-effect models based on heterogeneity.
Main Results:
- The hOGG1 Ser326Cys polymorphism was significantly associated with an increased risk of HCC across various genetic models (e.g., GG vs. CC: OR=2.51, 95% CI=1.67-3.78).
- Subgroup analyses by ethnicity indicated a higher HCC risk in Asians with GG and GG+CG genotypes.
- The association remained significant in both hospital-based and population-based control groups.
Conclusions:
- The hOGG1 Ser326Cys polymorphism is confirmed to be associated with an elevated risk of hepatocellular carcinoma.
- This finding contributes to a clearer understanding of the genetic factors influencing HCC development.
Background:
Since, the relationship between hOGG1 Ser326Cys polymorphism and HCC was inconsistent in the recent literatures. The present meta-analysis based on previous studies was to obtain precise estimation on the issue.
Methods:
A computer search was carried out from PubMed, CBM and EMBASE databases. A total of nine case-control publications with 2583 HCC patients and 2271 controls were included in the meta-analysis. Pooled odds ratios (ORs) and 95% confidence intervals (CIs) were calculated to evaluate the relationship of Ser326Cys polymorphism and HCC susceptibility. Z test was used to assess the significance of pooled OR. The fixed-effect model or random-effect model was employed according to heterogeneity.
Results:
Overall, hOGG1 Ser326Cys polymorphism was in relation with increased risk for HCC under the following genetic models: GG versus CC: OR=2.51, 95% CI=1.67-3.78; GG versus CG + CC: OR=2.27, 95% CI=1.57-3.30; GG + CG versus CC: OR=1.13, 95% CI=1.03-1.24. The subgroup analysis by ethnicity suggested that high risk for HCC was observed in Asians with GG and GG + CG genotype (GG versus CC: OR=2.17, 95% CI=1.49-3.17; GG versus CG + CC: OR=1.96, 95% CI=1.41-2.73; GG + CG versus CC: OR=1.13, 95% CI=1.03-1.25). For subgroup analysis based on source of control, GG genotype of Ser326Cys was significantly associated with HCC risk in hospital-based (HB) controls (GG versus CC: OR=2.31, 95% CI=1.50-3.56; GG versus CG + CC: OR=2.17, 95% CI=1.44-3.28), as well as in population-based (PB) models (GG vs. CC: OR=2.80, 95% CI=1.16-6.77; GG versus CG + CC: OR=2.39, 95% CI=1.08-5.30).
Conclusions:
According to the results, hOGG1 Ser326Cys polymorphism was associated with increased risk of HCC.
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