检索规则说明:AND代表“并且”;OR代表“或者”;NOT代表“不包含”;(注意必须大写,运算符两边需空一格)
检 索 范 例 :范例一: (K=图书馆学 OR K=情报学) AND A=范并思 范例二:J=计算机应用与软件 AND (U=C++ OR U=Basic) NOT M=Visual
作 者:王辉云[1] 严瑞琪[1] 龙江斌[1] 吴秋良[1]
机构地区:[1]中山医科大学肿瘤防治中心
出 处:《世界华人消化杂志》1999年第2期98-100,共3页World Chinese Journal of Digestology
基 金:国家教委博士学科点专项科研基金;广东省自然科学基金
摘 要:目的探讨癌基因cyclinD1在肝癌发生发展中的作用以及与HBV感染和临床病理之间的关系.方法取手术切除的肝细胞癌标本,用Southern杂交的方法对cyclinD1和CDK4癌基因以及HBV的感染状态进行了检测,切片同时行病理检查.结果肝癌39例中9例cyclinD1存在2~30倍的扩增(237%),其中1例检出重组杂交带;37例中5例(135%)有CDK4的扩增;HBVDNA在肝癌组织中检出的阳性率为947%,HBVDNA整合率为744%.相关分析发现,cyclinD1的扩增与CDK4扩增,HBVDNA整合,肿瘤的分化高低和肿块大小等之间有相关关系,相关系数r分别为051,031,039和055,全部P<005.结论cyclinD1的扩增与HBVDNA的整合密切相关,并在肝癌的恶化进展中起着重要作用.AIM To explore the amplification of cyclin D1 and its correlation to HBV infection and pathology during the development of human hepatocellular carcinoma (HCC). METHODS Forty specimens of fresh paired tumor and nontumor liver tissues from surgical resections were used for detection of genetic alterations of cyclin D1 , CD K 4 and HBV infection by the Southern hybridization. The samples were also examined histologically for pathological correlation with the genetic changes. RESULTS Two to thirty fold amplifications of cyclin D1 gene were detected in 9 of 39 HCC samples (23 7%) and a structural aberration of the gene was found in one of those samples with amplification. The amplifications of CD K 4 gene were found in 5 of 37 HCC cases. HBV DNA was detected in 37 of 39 HCC samples (94 9%) and the integration of HBV DNA in 29 of 39 HCC samples (74 4%). By correlation analysis, cyclin D1 amplification significantly correlated with amplification of CD K 4, the integration of HBV DNA, the differentiation degree and size of tumors. The correlation coefficients were 0 51, 0 31,0 39 and 0 55 respectively, P <0 05 for all. CONCLUSION The amplification of cyclin D1 is related to HBV DNA integration and plays an important role in the development and progression of HCC.
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在载入数据...
正在链接到云南高校图书馆文献保障联盟下载...
云南高校图书馆联盟文献共享服务平台 版权所有©
您的IP:18.118.32.150