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Combined core promoter mutations and pre-S deletion of HBV may not increase the risk of HCC: A geographical epidemiological study in Guangxi, China

机译:结合的核心启动子突变和HBV前S缺失可能不会增加HCC的风险:中国广西的一项地理流行病学研究

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摘要

Background: Although persistent hepatitis B virus (HBV) infection is a major cause of hepatocellular carcinoma (HCC), the mechanisms of oncogenesis remain obscure. Aims: To determine whether the findings that HBV basal core promoter (BCP) A1762T, G1764A double mutations, pre-S deletions and a combination of both are risk factors of HCC are supported by geographical epidemiology. Methods: Study subjects were recruited from Long An county, where the incidence of HCC is the highest, and five other counties in Guangxi, where the HCC incidence is lower and varies among them. The Pre-S region and BCP of HBV from all study subjects were amplified and sequenced and the data were analysed using chi-squared tests. Results: The prevalence of BCP and pre-S mutations differs significantly (χ2 = 9.850, 5.135, respectively, all P 0.01) between Long An and the other counties. However, the prevalence of combined BCP and pre-S mutations does not differ significantly (χ2 = 1.510, P 0.05). These mutations are less frequent in the young but the prevalence of pre-S deletions does not increase with age. The prevalence of these mutations does not differ significantly between men and women but is significantly higher in Zhuang than the other ethnic populations. Among the other five counties, the prevalence of BCP mutations in counties where the HCC incidence is high is significantly higher than that of counties where the HCC incidence is low. Conclusions: Combined BCP double mutations and pre-S deletion may not increase the risk of HCC, although these mutations are a risk factor of HCC when they present alone.
机译:背景:尽管持续的乙型肝炎病毒(HBV)感染是肝细胞癌(HCC)的主要原因,但其致癌机制仍然不清楚。目的:确定地理流行病学是否支持HBV基础核心启动子(BCP)A1762T,G1764A双重突变,pre-S缺失和两者结合是HCC的危险因素的发现。方法:研究对象来自肝癌发病率最高的隆安县和广西肝癌发病率较低且差异较大的广西其他五个县。所有研究对象的HBV的Pre-S区域和BCP进行扩增和测序,并使用卡方检验分析数据。结果:龙安县与其他县之间的BCP和pre-S突变的患病率差异显着(χ2= 9.850,5.135,所有P <0.01)。但是,合并的BCP和pre-S突变的患病率没有显着差异(χ2= 1.510,P> 0.05)。这些突变在年轻人中较不常见,但前S缺失的患病率不会随着年龄的增长而增加。这些突变的患病率在男性和女性之间没有显着差异,但在壮族地区则明显高于其他种族。在其他五个县中,HCC发生率高的县的BCP突变发生率显着高于HCC发生率低的县的BCP突变发生率。结论:BCP双重突变和pre-S缺失的组合可能不会增加HCC的风险,尽管这些突变单独出现时是HCC的危险因素。

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