## Abstract Interleukin‐23 (IL‐23)/IL‐23 receptor (IL‐23R) is essential for Th17 cell‐mediated immune response, involved in autoimmune diseases and cancer pathogenesis. Two potentially functional genetic single nucleotide polymorphisms (SNPs; __IL‐23R__ rs6682925 T>C and rs1884444 T>G) were found t
IL12 polymorphisms, HBV infection and risk of hepatocellular carcinoma in a high-risk Chinese population
✍ Scribed by Li Liu; Yan Xu; Zheng Liu; Jianguo Chen; Yixin Zhang; Jian Zhu; Jibin Liu; Sheng Liu; Guozhong Ji; Haibin Shi; Hongbing Shen; Zhibin Hu
- Publisher
- John Wiley and Sons
- Year
- 2010
- Tongue
- French
- Weight
- 140 KB
- Volume
- 128
- Category
- Article
- ISSN
- 0020-7136
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✦ Synopsis
Abstract
To investigate the association between the potentially functional polymorphisms in IL12A and IL12B, HBV infection and risk of hepatocellular carcinoma in a Chinese population, we genotyped three polymorphisms, rs568408 (3′UTR G>A), rs2243115 (5′UTR T>G) in IL12A and rs3212227 (3′UTR A>C) in IL12B in a case–control study of 869 hepatocellular carcinoma (HCC) cases and 891 cancer‐free controls. We found that the IL12A rs568408 GA/AA variant genotypes were associated with a significantly increased risk of HCC (adjusted odds ratio (OR) = 1.53, 95% confidence interval (CI) = 1.17–2.00), compared with the wild‐type GG homozygote. In the stratified analyses, the increased risk of HCC associated with rs568408 GA/AA was more evident in patients who were negative for HBsAg (adjusted OR = 1.71, 95% CI = 1.23–2.39). However, no significant associations between IL12A rs2243115 T/G, IL12B rs3212227 A/C and risk of HCC were observed. Our findings indicate that IL12A rs568408 may contribute to the risk of HCC and modify HCC risk associated with HBV infection.
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