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人类白细胞抗原DRA基因多态性与肝细胞癌遗传易感性的关联研究
引用本文:王孝焱,孙玉洁,张腾腾,邓阳.人类白细胞抗原DRA基因多态性与肝细胞癌遗传易感性的关联研究[J].现代预防医学,2020,0(23):4404-4407.
作者姓名:王孝焱  孙玉洁  张腾腾  邓阳
作者单位:山东第一医科大学(山东省医学科学院)公共卫生学院,山东 泰安 271016
摘    要:目的 探讨人类白细胞抗原DRA基因(human leukocyte antigen DRA,HLA-DRA)单核苷酸多态性(single nucleotide polymorphism,SNP)与肝细胞癌(Hepatocellular carcinoma,HCC)易感性的关联。方法 采用以医院为来源的非匹配病例对照研究方法,纳入365例HCC患者作为病例组以及365例非HCC患者作为对照组。利用问卷收集研究对象的一般人口学特征和相关暴露因素资料,并采用TaqMan-MGB探针定量PCR法对rs3135395 G>T、rs3135338 T>C和rs2395178 G>C进行基因型检测。应用非条件logistic回归模型计算SNP位点各基因型与HCC易感性的比值比(odds ratio,OR)及95%可信区间(confidence interval,CI)。结果 携带rs3135338 TC基因型和显性模型(TC+CC)的个体HCC易感性较TT基因型携带者显著降低(OR=0.47,95% CI=0.25~0.91,P=0.024;OR=0.53,95% CI=0.28~0.95,P=0.045)。与rs2395178 GG基因型携带者相比,GC基因型和显性模型(GC+CC)携带者HCC易感性显著降低(OR=0.41,95% CI=0.29~0.57,P<0.001;OR=0.58,95% CI=0.41~0.81,P=0.002)。结论 HLA-DRA基因rs3135338 T>C和rs2395178 G>C与HCC易感性相关,可为揭示免疫相关基因遗传多态性对HCC发生的作用提供一定参考。

关 键 词:肝细胞癌  人类白细胞抗原DRA  单核苷酸多态性  遗传易感性

Association between Human leukocyte antigen DRA gene polymorphisms and susceptibility to hepatocellular carcinoma
WANG Xiao-yan,SUN Yu-jie,ZHANG Teng-teng,DENG Yang.Association between Human leukocyte antigen DRA gene polymorphisms and susceptibility to hepatocellular carcinoma[J].Modern Preventive Medicine,2020,0(23):4404-4407.
Authors:WANG Xiao-yan  SUN Yu-jie  ZHANG Teng-teng  DENG Yang
Institution:School of Public Health, Shandong First Medical University & Shandong Academy of Medical Sciences, Tai’an, Shandong 271016, China
Abstract:Objective To investigatethe association between single nucleotide polymorphism (SNP) of human leukocyte antigen DRA (HLA-DRA) gene and susceptibility to hepatocellular carcinoma (HCC). WTHZ]Methods A hospital-based non-matched case-control study was conducted among 365 patients with HCC as a case group and 365 patients without HCC as a control group. The questionnaire was used to collect the general demographic characteristics and relevant exposure factors, and the TaqMan-MGB probe quantitative PCR method was performed to detect the genotypes of rs3135395 G>T, rs3135338 T>C, and rs2395178 G>C. The unconditional logistic regression model was used to calculate the odds ratio (OR) and 95% confidence interval (CI) of each genotype of SNP to HCC susceptibility. WTHZ]Results Subjects with rs3135338 TC genotype and dominant model (TC+CC) were significantly less susceptible to HCC than TT genotype carriers (OR=0.47, 95% CI=0.25-0.91, P=0.024; OR=0.53, 95% CI=0.28-0.95, P=0.045). Compared with rs2395178 GG genotype carriers, subjects with GC genotype and dominant model (GC+CC) had significantly lower HCC susceptibility (OR=0.41, 95% CI=0.29-0.57, P<0.001; OR=0.58, 95% CI=0.41-0.81, P=0.002). WTHZ]Conclusion HLA-DRA rs3135338 T>C and rs2395178 G>C are associated with HCC susceptibility, which can provide a reference for revealing the role of genetic polymorphisms of immune-related genes on the occurrence of HCC.
Keywords:Hepatocellular carcinoma  Human leukocyte antigen DRA  Single nucleotide polymorphism  Genetic susceptibility
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