Suppr超能文献

通过非放射性原位杂交检测肝癌细胞系中整合的乙型肝炎病毒DNA

Detection of integrated hepatitis B virus DNA in hepatocellular carcinoma cell lines by nonradioactive in situ hybridization.

作者信息

Tay N, Chan S H, Ren E C

机构信息

Department of Microbiology, Faculty of Medicine, National University of Singapore.

出版信息

J Med Virol. 1990 Apr;30(4):266-71. doi: 10.1002/jmv.1890300407.

Abstract

A sensitive and specific nonradioactive in situ hybridization method capable of detecting single-copy integrated hepatitis B virus (HBV) DNA sequences in hepatocellular carcinoma (HCC) cell lines was developed. In situ hybridization of biotinylated HBV (adr, adw) DNA probes with nine different human HCC cell lines were carried out in 96-well microtiter plates. Integration was detected in HCC cell lines HCCM, Hep3B, huH-1, huH-4, and PLC/PRF/5. Detection of single-copy HBV DNA sequences was also achieved in Hep3B and huH-4. HCC cell lines HepG2, HUH-6, HUH-7, Mahlavu, and the non-HCC control MCF-7, gave clear negative results. These results show a 100% correlation with those obtained by Southern blot hybridization assay. The results demonstrate that nonradioactive detection of single-copy integrated HBV DNA sequences in HCC cell lines is possible by the method described, which has potential application for viral genome analysis requiring in situ hybridization.

摘要

我们开发了一种灵敏且特异的非放射性原位杂交方法,该方法能够检测肝癌(HCC)细胞系中的单拷贝整合型乙型肝炎病毒(HBV)DNA序列。在96孔微量滴定板中,用生物素化的HBV(adr,adw)DNA探针与九种不同的人肝癌细胞系进行原位杂交。在肝癌细胞系HCCM、Hep3B、huH-1、huH-4和PLC/PRF/5中检测到了整合情况。在Hep3B和huH-4中也实现了单拷贝HBV DNA序列的检测。肝癌细胞系HepG2、HUH-6、HUH-7、Mahlavu以及非肝癌对照MCF-7均给出了明确的阴性结果。这些结果与通过Southern印迹杂交分析获得的结果显示出100%的相关性。结果表明,通过所述方法可以对肝癌细胞系中的单拷贝整合型HBV DNA序列进行非放射性检测,该方法在需要原位杂交的病毒基因组分析中具有潜在应用价值。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验