Abstract
Objective
TNF-α-308 G/A, TNF-α-238 G/A, IL-1B-31 T/C, IL-1B-511 C/T, and IL-10-1082 G/A polymorphisms have been reported to influence the risk for hepatocellular carcinoma (HCC) in many studies; however, the results still remains controversial and ambiguous. The aim of this study was to determine more precise estimations for the relationship between TNF-α, IL-1B, and IL-10 polymorphisms and the risk for HCC by meta-analysis.
Methods
Electronic searches for all publications were conducted on associations between these variants and HCC in several databases through September 2010. Odds ratios (OR) with 95% confidence intervals (95% CI) were calculated to estimate the strength of this association in a random-effect model. Twenty studies were identified, involving 2,763 HCC patients and 4,152 controls.
Results
This meta-analysis showed significant association between TNF-α-308 polymorphism and HCC (AA + GA vs. GG: OR = 1.74, 95% CI = 1.12–2.72). In Caucasian and Asian subgroups, OR values (95% CI) were 1.49 (0.58–3.82) and 1.84 (1.06–3.20), respectively. While the ORs for TNF-α-238 G/A, IL-1B-31 T/C, -511 C/T and IL-10-1082 G/A polymorphisms and HCC were 1.37 (0.95–2.00), 1.24 (0.99–1.55), 1.12 (0.66–1.88) and 0.91 (0.74–1.12), respectively. The sensitivity analysis further strengthened the overall strong positive correlations. No publication bias was observed in this study.
Conclusions
TNF-α-308 G/A polymorphism is assumed to confer a higher risk for HCC, especially in Asian population. TNF-α-238 G/A, IL-1B-31 T/C, -511 C/T, and IL-10-1082 G/A polymorphisms were not detected to be related to the risk for HCC.
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Acknowledgments
This work was supported by Harbin Special Funds for Research of Scientific and Technological Innovative Talents (No. RC2011QN004139).
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The authors do not have any conflicts of interest to report with for this manuscript.
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Yu Yang and Chao Luo contributed equally to this work.
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Yang, Y., Luo, C., Feng, R. et al. The TNF-α, IL-1B and IL-10 polymorphisms and risk for hepatocellular carcinoma: a meta-analysis. J Cancer Res Clin Oncol 137, 947–952 (2011). https://doi.org/10.1007/s00432-010-0959-8
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DOI: https://doi.org/10.1007/s00432-010-0959-8