首页> 外文期刊>Journal of Medical Virology >Expression Quantitative Trait Loci for TNFRSF10 Influence Both HBV Infection and Hepatocellular Carcinoma Development
【24h】

Expression Quantitative Trait Loci for TNFRSF10 Influence Both HBV Infection and Hepatocellular Carcinoma Development

机译:TNFRSF10的表达定量特征位点影响HBV感染和肝细胞癌的发展。

获取原文
获取原文并翻译 | 示例
           

摘要

Tumor necrosis factor receptor superfamily member 10 (TNFRSF10) is a death domaincontaining receptor for the apoptotic ligand TNFSF10, which involves multiple processes, including hepatocarcinogenesis and immune response against HBV infection. Several single nucleotide polymorphisms (SNPs) were identified as expression quantitative trait loci (eQTLs) for TNFRSF10. To assess the association of TNFRSF10 eQTL SNPs with the risk of hepatocellular carcinoma (HCC) and chronic HBV infection, we designed a case-control study that included 1,300 HBV-related HCC patients, 1,344 chronic HBV carriers, and 1,344 subjects with HBV natural clearance, and then genotyped two TNFRSF10 eQTL SNPs (rs79037040 and rs2055822). We found that rs79037040 GT/TT genotypes were associated with a decreased HCC risk (adjusted odds ratio [OR] = 0.83, 95% confidence intervals [CIs] = 0.71-0.97, P = 0.021) but an increased chronic HBV infection risk of borderline significance (adjusted OR = 1.14, 95% CIs = 0.98-1.33, P = 0.085). In contrast, the rs2055822 G allele was a risk factor for HCC (adjusted OR = 1.12, 95% CIs = 1.00-1.25, P = 0.041) but a protective factor for chronic HBV infection (adjusted OR = 0.89, 95% CIs = 0.80-0.99, P = 0.038). Furthermore, we observed a dose-dependent relationship between the number of alleles (rs79037040-T and rs2055822-A) and the risk of HCC and chronic HBV infection. In comparison with "0" alleles, having "1-4" alleles was significantly associated with decreased HCC risk and increased HBV infection risk. These findings suggest that eQTL SNPs for TNFRSF10 may be susceptibility markers for HCC and chronic HBV infection. (C) 2015 Wiley Periodicals, Inc.
机译:肿瘤坏死因子受体超家族成员10(TNFRSF10)是包含凋亡域配体TNFSF10的死亡域受体,涉及多个过程,包括肝癌发生和针对HBV感染的免疫反应。几个单核苷酸多态性(SNP)被确定为TNFRSF10的表达定量性状基因座(eQTL)。为了评估TNFRSF10 eQTL SNP与肝细胞癌(HCC)和慢性HBV感染风险的相关性,我们设计了一项病例对照研究,其中包括1,300例与HBV相关的HCC患者,1,344例慢性HBV携带者和1,344例具有HBV自然清除率的受试者,然后对两个TNFRSF10 eQTL SNP(rs79037040和rs2055822)进行基因分型。我们发现rs79037040 GT / TT基因型与降低的HCC风险相关(校正比值比[OR] = 0.83,95%置信区间[CIs] = 0.71-0.97,P = 0.021),但慢性HBV感染的危险性增加显着性(调整后的OR = 1.14,95%CIs = 0.98-1.33,P = 0.085)。相比之下,rs2055822 G等位基因是HCC的危险因素(调整后OR = 1.12,95%CIs = 1.00-1.25,P = 0.041),但是慢性HBV感染的保护因素(调整后OR = 0.89,95%CIs = 0.80) -0.99,P = 0.038)。此外,我们观察到等位基因数目(rs79037040-T和rs2055822-A)与HCC和慢性HBV感染的风险之间存在剂量依赖性关系。与“ 0”等位基因相比,“ 1-4”等位基因与降低的HCC风险和增加的HBV感染风险显着相关。这些发现表明,TNFRSF10的eQTL SNP可能是HCC和慢性HBV感染的易感性标志物。 (C)2015威利期刊公司

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号