Author:
Ma S.,Wu J.,Wu J.,Wei Y.,Zhang L.,Ning Q.,Hu D.
Abstract
Objective: We explored the relationship between HLA-DRB1 allele polymorphisms and familial aggregation of hepatocellular carcinoma (fHCC). Methods: Polymerase chain reaction sequence-specific primers were used to determine HLA-DRB1 genotypes for 130 members of families with 2 or more liver cancer patients and for 130 members of families without any diagnosed cancers. The genotype profiles were then compared to explore the relationship between HLA-DRB1 gene polymorphism and fHCC. Result: Of 11 selected alleles, the frequencies of DRB1*11 and DRB1*12 were significantly lower in the fHCC group than in no-cancer group (p < 0.05; odds ratio: 0.286; 95% confidence interval: 0.091 to 0.901; and odds ratio: 0.493; 95% confidence interval: 0.292 to 0.893). Differences in the frequencies of the other 9 alleles were not statistically significant in the two groups (p > 0.05). Conclusions: Our research suggests that if genetic factors play a role in fHCC, the deficiency in the DRB1*11 and DRB1*12 alleles might be the risk factor at work in Guangxi Zhuang Autonomous Region, P.R.C.
Cited by
7 articles.
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