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作 者:丁红芳[1] 田德英[1] 杨道锋[1] 皮斌[1] 许东[1]
机构地区:[1]华中科技大学同济医学院附属同济医院感染科,湖北武汉430030
出 处:《中西医结合肝病杂志》2006年第4期206-209,共4页Chinese Journal of Integrated Traditional and Western Medicine on Liver Diseases
摘 要:目的:研究肝细胞癌(HCC)患者乙型肝炎病毒(HBV)基因型与基本核心启动子(BCP)基因区A1762T/G1764A双位点变异(BCP区双突变)之间的关系,探讨HCC的发病机制。方法:选择40例HCC患者作为研究组,40例慢性乙型肝炎(CHB)患者作为对照组,采用多对型特异性引物PCR扩增法进行基因分型及HBV基因多态性芯片检测BCP区A1762T/G1764A双位点变异。结果:40例HCC患者中有30例HBV DNA定量阳性,平均对数值为(6·53±1·31)copy/ml,将30例HBV DNA定量阳性的HCC及40例CHB患者的血清进行HBV基因分型及基因变异检测,结果显示30例HCC中HBV B基因型5例(16·7%),C基因型25例(83·3%);BCP区双突变共有20例(67·7%),其中B基因型1例,C基因型19例,BCP双突变率在B基因型和C基因型中分别为20%(1/5)和76%(19/25);40例CHB患者中B基因型32例(80%),C基因型8例(20%);BCP区双突变共有13例,其中B基因型8例,C基因型5例,BCP双突率在B基因型和C基因型中分别是25%(8/32)和62·5%(5/8)。结论:肝细胞癌的发生与BCP区A1762T/G1764A双位点变异有关,多发生在HBV C基因型的患者。Objective: To investigate the relationships between hepatitis B virus (HBV) genotype and HBV core promoter mutants, and in order to explore the pathogenesis of hepatocellular carcinoma. Methods: Serum samples from 40 patients with hepatoma and 40 patients with chronic hepatitis B (CHB) were collected and tested for HBV genotypes by the multiplex typespecific primers, Signal-base mutations of G1896A. A1762T and G1764A were analyzed by gene chips technique. Results: There were 30 cases in the 40 HCC patients whose HBV DNA quantification were positive, the average levels of the HBV DNA quantification were (6. 53 ± 1.31 ) copy/ml (Logarithm) . The HBV genotypes and HBV mutants were tested for the 30 HCC and 40 CHB patients, the results showed that in the 30 HCC cases, 5 ( 16. 7% ) were genotype B, 25 (83.3%) were genotype C; Twenty of the 30 HCC patients were found to have mutants in HBV BCP region at nucleotide A1762T/G1764A, among which 1 case were detected with genotype B and 19 cases with genotype C ( 20% VS 76% , P 〈 0. 05 ) . In the 40 CHB patients, the percentagens of genotype B and C were 80%, 20% respectively, 13 of 40 CHB patients were found to have mutants in BCP region, among which 8 cases were genotype B and 5 cases with genotype C. Conclusion: The genotype C is the predominant genotype in HBV related HCC, and there are a clear link between HBV genotype and HBV BCP mutants at nucleotide A1762T/ G1764A in hepatoma.
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