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Toll样受体3基因变异与肝细胞癌及乙肝相关肝细胞癌的易感性

Toll-like receptor 3 genetic variants and susceptibility to hepatocellular carcinoma and HBV-related hepatocellular carcinoma.

作者信息

Li Guanggang, Zheng Zhendong

机构信息

Department of ICU, General Hospital of Beijing Military Command, Beijing, 100700, China.

出版信息

Tumour Biol. 2013 Jun;34(3):1589-94. doi: 10.1007/s13277-013-0689-z. Epub 2013 Feb 13.

Abstract

Hepatocellular carcinoma (HCC) is a highly aggressive cancer with few treatment options. Toll-like receptor 3 (TLR3) plays a key role in innate immunity and may affect the development of cancers. This study aimed to investigate whether TLR3 polymorphisms were associated with susceptibility to HCC. Two polymorphisms in the TLR3 gene, -976T/A and +1234C/T, were tested by polymerase chain reaction-restriction fragment length polymorphism in 466 HCC patients and 482 healthy controls. Results showed that the prevalence of +1234CT genotype and +1234TT genotype were significantly increased in the HCC cases than in controls (odds ratio [OR] =1.51; 95 % confidence interval [CI]; 1.22-1.93; p=0.004 and OR=3.19; 95 % CI, 1.82-5.39; p=1.99 × 10(-5), respectively). The -976T/A polymorphism did not reveal any differences between cases and controls. When analyzing the TLR3 +1234C/T polymorphism with different clinical parameters in HCC patients, the cases who were hepatitis B virus (HBV) carriers had higher number of +1234CT genotype and +1234T allele than those without HBV infection (p=0.032 and p=0.043). These data indicate that TLR3 +1234C/T polymorphism could be a novel risk factor for HCC, especially the HBV-related HCC.

摘要

肝细胞癌(HCC)是一种侵袭性很强的癌症,治疗选择有限。Toll样受体3(TLR3)在先天免疫中起关键作用,可能影响癌症的发展。本研究旨在探讨TLR3基因多态性是否与HCC易感性相关。通过聚合酶链反应-限制性片段长度多态性方法,对466例HCC患者和482例健康对照者检测了TLR3基因的两个多态性位点-976T/A和+1234C/T。结果显示,HCC患者中+1234CT基因型和+1234TT基因型的患病率显著高于对照组(优势比[OR]=1.51;95%置信区间[CI]:1.22-1.93;p=0.004;OR=3.19;95%CI:1.82-5.39;p=1.99×10⁻⁵)。-976T/A多态性在病例组和对照组之间未显示出任何差异。在分析HCC患者TLR3 +1234C/T多态性与不同临床参数的关系时,乙型肝炎病毒(HBV)携带者的+1234CT基因型和+1234T等位基因数量高于未感染HBV的患者(p=0.032和p=0.043)。这些数据表明,TLR3 +1234C/T多态性可能是HCC的一个新的危险因素,尤其是与HBV相关的HCC。

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