首页> 外文期刊>Immunological Investigations: A Journal of Molecular and Cellular Immunology >Autophagy-Related 5 Gene rs510432 Polymorphism Is Associated with Hepatocellular Carcinoma in Patients with Chronic Hepatitis B Virus Infection
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Autophagy-Related 5 Gene rs510432 Polymorphism Is Associated with Hepatocellular Carcinoma in Patients with Chronic Hepatitis B Virus Infection

机译:相关5基因RS510432多态性与慢性乙型肝炎病毒感染患者的肝细胞癌有关

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Background: Despite the identification of autophagy-related protein 5 (ATG5) as a molecule involved in the activated autophagy machinery during hepatitis B virus (HBV) infection and hepatocarcinogenesis, the consequences of ATG5 mutation carriage for patients with chronic HBV infection remain unclear. This study examined the association of ATG5 polymorphisms with HBV-related diseases including hepatocellular carcinoma (HCC). Patients and Methods: Two functionally relevant polymorphisms ATG5 rs573775 and rs510432 were genotyped by ligase detection reaction-polymerase chain reaction in 403 patients with chronic HBV infection (171 chronic hepatitis, 119 cirrhosis and 113 HCC) and 196 healthy controls. Univariate and multivariate logistic regression was performed to evaluate factors associated with HCC. Results: The rs573775 genotype and allele frequencies had no significant differences between patients with different clinical diseases. However, HCC patients had significantly higher frequency of rs510432 genotype AA (odds ratio [OR] 2.185, 95% confidence interval [CI] 1.042–4.581, P = 0.037, P value by Bonferroni correction [P c ] = 0.074) and allele A (OR 1.435, 95% CI 1.023–2.013, P c = 0.036) than chronic hepatitis patients. In multivariate analyses, rs510432 allele A-containing genotypes (AA+GA) were independently associated with cirrhosis in comparison to chronic hepatitis (OR 1.927, 95%CI 1.011–3.017, P = 0.032). The rs510432 genotypes AA+GA were also independently associated with HCC in comparison to chronic hepatitis (OR 2.583, 95% CI 1.025–3.911, P = 0.006) or chronic HBV infection without HCC (OR 2.632, 95% CI 1.067–3.482, P = 0.032). Conclusion: These results indicate that rs510432 genotypes AA+GA are associated with disease progression and HCC risk in chronic HBV infection, providing novel evidence for a role of ATG5 in the pathogenesis of HBV-related HCC. Abbreviations: HBV: hepatitis B virus; HCC hepatocellular carcinoma; TNFSF10: tumor necrosis factor superfamily member 10; ATG5: autophagy-related protein 5; DNA: deoxyribonucleic acid; LDR-PCR: ligase detection reactions-polymerase chain reaction; PCR: polymerase chain reaction; SLE: systemic lupus erythematosus; BD: Beh?et’s disease; IL-10: interlukin-10; LPS: lipopolysaccharide; PBMC: peripheral blood mononuclear cells; CWP: coal workers’ pneumoconiosis; TNF-α: tumor necrosis factor-α.
机译:背景:尽管鉴定了与乙型肝炎病毒(HBV)感染和肝癌发生期间活性自噬机械中涉及的分子鉴定了自噬相关蛋白5(ATG5),但慢性HBV感染患者的ATG5突变携带的后果仍不清楚。该研究检测了与肝细胞癌(HCC)在内的HBV相关疾病的ATG5多态性的关联。患者和方法:两种功能相关的多态性ATG5 RS573775和RS510432在403例慢性HBV感染患者中通过连接酶检测反应 - 聚合酶链反应进行基因分型(171次慢性肝炎,119肝功能,113 HCC)和196例健康对照。进行单变量和多变量逻辑回归,以评估与HCC相关的因素。结果:RS573775基因型和等位基因频率在不同临床疾病的患者之间没有显着差异。然而,HCC患者的频率明显高,RS510432基因型AA(差距[或] 2.185,95%,95%置信区间[CI] 1.042-4.581,P = 0.037,P值By Bonferroni校正[P C] = 0.074)和等位基因a (或1.435,95%CI 1.023-2.013,P C = 0.036)比慢性肝炎患者。在多变量分析中,与慢性肝炎(或1.927,95%CI 1.011-3.017,P = 0.032,P = 0.032,P = 0.032,P = 0.032,P = 0.032)与含含含基因型(AA + Ga)与肝硬化独立相关。与慢性肝炎(或2.583,95%CI 1.025-3.911,P = 0.006)或没有HCC的慢性HBV感染,RS510432基因型AA + Ga也与HCC独立相关,无HCC(或2.632,95%CI 1.067-3.482,P = 0.032)。结论:这些结果表明,RS510432基因型AA + GA与慢性HBV感染中的疾病进展和HCC风险有关,为ATG5在HBV相关HCC发病机制中提供了新的依据。缩写:HBV:乙型肝炎病毒; HCC肝细胞癌; TNFSF10:肿瘤坏死因子超家族成员10; ATG5:与自噬相关的蛋白5; DNA:脱氧核糖核酸; LDR-PCR:连接酶检测反应 - 聚合酶链反应; PCR:聚合酶链反应; SLE:Systemic Lupus erythematosus; BD:Beh?等IL-10:Interlukin-10; LPS:Lipopolysaccharide; PBMC:外周血单核细胞; CWP:煤炭工人的肺炎; TNF-α:肿瘤坏死因子-α。

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