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与持续 HBV 感染患者原发性肝细胞癌相关的人类白细胞抗原 I 类等位基因和单倍型。

Human leukocyte antigen class I alleles and haplotypes associated with primary hepatocellular carcinoma in persistent HBV-infected patients.

机构信息

Department of Immunology and Pathogen Biology, Medical School, Southeast University, Nanjing 210009, China.

出版信息

Hum Immunol. 2013 Jun;74(6):758-63. doi: 10.1016/j.humimm.2013.02.007. Epub 2013 Mar 1.

Abstract

Many studies have shown that Human leukocyte antigen (HLA) class I alleles are associated with the development of various cancers. However, its role in hepatocellular carcinoma (HCC) is still unknown. To investigate whether HLA class I allelic polymorphism is related to the development of hepatitis B virus(HBV)-associated HCC, a total of 326 HBV-infected patients (138 individuals with HCC and 188 well-matched controls without HCC) were enrolled in this study. HLA-A, -B, and -C were genotyped by polymerase chain reaction-sequencing based typing (PCR-SBT) method. We identified HLA-B(∗)35:01:01G as a risk factor for HBV-related HCC development independent of our previous findings in HLA region (OR, 12.04; p, 0.0028; pc, 0.04). HLA-A(∗)11:01:01G, B(∗)58:01:01G, C(∗)03:02:01G and some of their extended haplotypes were found as potential susceptible factors for HCC development. HLA-B(∗)46:01:01G and some of its extended haplotypes were found as potential protective factors for HCC development. Our results support that specific HLA class I alleles and haplotypes may affect the risk of HBV-related HCC development. The findings may help to determine better approaches for prevention and treatment of HCC in these patients.

摘要

许多研究表明,人类白细胞抗原(HLA)I 类等位基因与各种癌症的发展有关。然而,其在肝细胞癌(HCC)中的作用尚不清楚。为了研究 HLA I 类等位基因多态性是否与乙型肝炎病毒(HBV)相关 HCC 的发生有关,本研究共纳入 326 例 HBV 感染患者(138 例 HCC 患者和 188 例无 HCC 的匹配对照)。采用聚合酶链反应-测序基序(PCR-SBT)方法对 HLA-A、-B 和-C 进行基因分型。我们发现 HLA-B(∗)35:01:01G 是 HBV 相关 HCC 发展的独立危险因素,与我们之前在 HLA 区域的发现无关(OR,12.04;p,0.0028;pc,0.04)。HLA-A(∗)11:01:01G、B(∗)58:01:01G、C(∗)03:02:01G 和它们的一些扩展单倍型被发现是 HCC 发展的潜在易感因素。HLA-B(∗)46:01:01G 和它们的一些扩展单倍型被发现是 HCC 发展的潜在保护因素。我们的结果支持特定的 HLA I 类等位基因和单倍型可能影响 HBV 相关 HCC 发展的风险。这些发现可能有助于为这些患者确定更好的 HCC 预防和治疗方法。

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