赵 璋,张 宁,龙 江.肝细胞癌基因组5q13.2与8p23.1位点的杂合性缺失分析[J].肿瘤学杂志,2015,21(1):34-38.
肝细胞癌基因组5q13.2与8p23.1位点的杂合性缺失分析
Loss of Heterozygosity in Two Distinct Regions,5q13.2 and 8p23.1 in Hepatocellular Carcinoma
投稿时间:2014-03-11  
DOI:10.11735/j.issn.1671-170X.2015.01.B008
中文关键词:  杂合性缺失  肝细胞癌  基因
英文关键词:loss of heterozygosity  hepatocellular carcinoma  gene
基金项目:王宝恩肝纤维化基金(20100013);北京市自然科学基金(7132058)
作者单位
赵 璋 首都医科大学附属北京友谊医院 
张 宁 首都医科大学附属北京友谊医院 
龙 江 首都医科大学附属北京佑安医院 
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中文摘要:
      摘 要:[目的] 分析肝细胞癌(HCC)中5q13.2和8p23.1位点的杂合性缺失(LOH)情况,以探索新的抑癌基因。[方法] 应用聚合酶链反应—非变性聚丙烯酰胺凝胶电泳法对83例HCC患者基因组DNA中的5q13.2和8p23.1位点的LOH进行检测,并将其与临床参数进行关联分析。[结果] 83例HCC患者基因组中,36.1%(30例)存在5q13.2位点LOH,在该位点存在OCLN、SMN2、SERF1A 、SMN1、NAIP和 GTF2H2基因;8p23.1的D8S503和D8S1130位点分别存在68.4%和61.3%的LOH。[结论] HCC患者基因组中存在较高频率的5q13.2和8p23.1位点LOH,这些位点中可能存在与HCC发生密切相关的基因。
英文摘要:
      Abstract:[Purpose] To investigate the frequency of loss of heterozygosity(LOH) at 5q13.2 and 8p23.1 in hepatocellular carcinoma (HCC),and to explore possible tumor suppressor genes in the loci.[Methods] The frequency of LOH at 5q13.2 and 8p23.1 were analyzed in 83 cases with HCC by polymerase chain reaction-polyacrylamide gel electrophoresis. Correlation analysis were performed between the frequency of LOH and clinicopathological characteristics of HCC.[Results] Thirty of 83 HCC cases were indentified with LOH(36.1%) at 5q13.2,where a series of functional genes were harbored such as OCLN,SMN2,SERF1A,SMN1,NAIP and GTF2H2. The frequencies of LOH at D8S1130 and D8S503 in 8p23.1 were 61.29% and 68.4% respectively.[Conclusion] In the genome of HCC,there are high frequency of LOH at 5q13.2 and 8p23.1,where critical genes associated with the development of HCC may harbor.
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