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原发性肝细胞癌与IL-2、IFN-γ基因多态性关系

Gene polymorphism of IL-2, IFN-gamma and primary hepatocellular carcinoma

  • 摘要: 目的 探讨细胞因子IL-2基因-330T/G(rs2069762)位点和IFN-γ基因-1615C/T(rs2069705)、+5171A/G(rs2069727)位点单核苷酸多态性与原发性肝细胞癌(HCC)发生的关系。方法 采用医院为基础的病例对照研究方法于2007年6月—2010年7月在广西医科大学第一附属医院和广西肿瘤医院收集784例HCC患者和同期在广西医科大学第一附属医院及广西区医院体检中心1 017名健康对照人群进行环境暴露调查;采用Taq-Man荧光定量PCR技术对上述位点进行分型,应用logistic回归模型分析组间基因-环境和基因-基因的交互作用。结果 IFN-γ的-1615C/T和+5171A/G位点存在连锁不平衡(D'=0.976,r2=0.549,P=2.22-16),单倍型CG在人群中发生频率<0.03,其他3种单倍型CA、TA、TG频率在病例组和对照组间分布差异均无统计学意义(P>0.05);IL-2-330T/GIFN-γ-1615C/T、+5171A/G3个位点的基因型在HCC患者和健康对照人群中分布差异均无统计学意义(P>0.05);吸烟、饮酒和携带HBV等环境暴露因素与-330T/G位点的突变基因G对HCC的发生有协同作用,交互作用指数S分别为1.38、1.50、1.03;吸烟、饮酒、有肝癌相关家族史和携带HBV等环境暴露因素与-1615C/T、+5171A/G位点的基因多态性在HCC患病风险中存在负交互作用;logistic回归分析结果表明,携带IL-2的-330T/G位点突变基因G并且同时携带IFN-γ的-1615C/T、+5171A/G位点的突变纯合子TT/GG能增加HCC患病风险(OR=1.84,95% CI=1.08~3.83)。结论 IL-2基因-330T/GIFN-γ基因-1615C/T、+5171A/G位点多态性与环境暴露因素存在交互作用,基因-环境、基因-基因交互作用可能增加HCC发生风险。

     

    Abstract: Objective To explore the association of interleukin-2(IL-2)-330T/G (rs2069762),interferon gamma (IFN-γ)-1615C/T(rs2069705) and +5171A/G(rs2069727) single nucleotide polymorphisms(SNPs) with the incidence of primary hepatocellular carcinoma(HCC),and to provide the reference for HCC risk assessment.Methods A hospital-based case-control study was carried out.Totally 784 HCC patients from First Affiliated Hospital of Guangxi Medical University and Guangxi Cancer Hospital and 1 017 controls from Physical Examination Center of First Affiliated Hospital of Guangxi Medical University and Guangxi People's Hospital were investigated with a environmental exposure questionnaire during June 2007-July 2010.TaqMan fluorescence quantitative PCR technology was adopted to detect the SNPs of the genes.The interactions of gene-environment and gene-gene w ere analyzed with logistic regression model.Results -1615C/T and +5171A/G of IFN-γ had linkage disequilibrium (D'=0.976,r2=0.549,P=2.22-16).The frequency of haplotype CG was less than 0.03 in the study population.CA,TA and TG had no statistically significant difference among the three groups(P > 0.05).There were no statistically significant differences in the polymorphisms of IL-2 -330T/G,IFN-γ-1615C/T and +5171A/G between HCC patients and controls(P > 0.05).The interactions of IL-2330T/G mutant allele G with smoking,alcohol drinking and carrying HBV were positive with the synergy indexes(S) of 1.38,1.50,and 1.03,respectively.The individuals carrying IL-2-330T/G mutant gene G and both IFN-gamma-1615C/T and +5171A/G mutant homozygote(TT and GG) had increased risk of HCC(odds ratio=1.84,95% confidence interval:1.08-3.83).Conclusion There are interactions among polymorphisms of IL-2-330T/G and IFN-γ-1615C/T,+5171A/G and the environmental exposure.The gene-environment and gene-gene interaction may increase the risk of HCC.

     

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