TNIP1 Polymorphisms with the Risk of Hepatocellular Carcinoma Based on Chronic Hepatitis B Infection in Chinese Han Population
Autor: | Qi Li, Chan Zhang, Jieqiong Jin, Xiongjian Luo, Xiaochun Jiang, Wanlu Chen, Yujing Cheng |
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Rok vydání: | 2018 |
Předmět: |
Male
0301 basic medicine China medicine.medical_specialty Carcinoma Hepatocellular Single-nucleotide polymorphism Biology Polymorphism Single Nucleotide Biochemistry Gastroenterology Linkage Disequilibrium 03 medical and health sciences Hepatitis B Chronic 0302 clinical medicine Internal medicine Genotype Genetic model Genetics medicine Humans Genetic Predisposition to Disease Allele Molecular Biology Ecology Evolution Behavior and Systematics Liver Neoplasms Haplotype Case-control study General Medicine Middle Aged medicine.disease digestive system diseases DNA-Binding Proteins 030104 developmental biology Case-Control Studies 030220 oncology & carcinogenesis Hepatocellular carcinoma Etiology Female |
Zdroj: | Biochemical Genetics. 57:117-128 |
ISSN: | 1573-4927 0006-2928 |
DOI: | 10.1007/s10528-018-9882-5 |
Popis: | Chronic hepatitis B virus (HBV) infection is an important etiology for the development of hepatocellular carcinoma (HCC). Tumor necrosis factor-α-induced protein 3-interacting protein 1 (TNIP1) is linked to specific inflammatory diseases as a novel type of endogenous inflammatory regulator. However, presently, rare information is found about the association between TNIP1 polymorphisms and HBV-induced HCC risk. In this case control study, we genotyped four single nucleotide polymorphisms (SNPs) in TNIP1 gene in 248 HCC patients and 242 chronic HBV carriers using Sequenom Mass-ARRAY technology. Genetic model and haplotype analysis were performed to evaluate the association between candidate SNPs polymorphisms and HBV-induced HCC susceptibility using Pearson's χ2 test and unconditional logistic regression analysis. Overall, we found two risk alleles in TNIP1 for HBV-induced HCC in patients: the allele "G" of rs7708392 by genotype model ("G/C" vs. "C/C": OR 1.88, 95% CI 1.17-3, P = 0.009) and dominant model ("G/C-G/G" vs. "C/C": OR 1.69, 95% CI 1.08-2.65, P = 0.023), and the allele "C" of rs10036748 by genotype model ("C/T" vs. "T/T": OR 1.83, 95% CI 1.14-2.92, P = 0.012) and dominant model ("C/T-C/C" vs. "T/T": OR 1.65, 95% CI 1.05-2.59, P = 0.03). However, rs3792792 and rs4958881 polymorphisms didn't significantly correlate with the risk of HBV-induced HCC. Haplotype analysis showed no significant association between haplotypes and the HCC risk in HBV carriers. This study provides evidence for HBV-induced HCC susceptibility gene TNIP1 in the Chinese Han population. |
Databáze: | OpenAIRE |
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