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Hepatitis B Virus DNA Detection by In Situ Hybridization in Human Hepatocellular Carcinoma

The distribution of hepatitis B virus (HBV) DNA in tumor tissue sections from six Korean patients with HBsAg positive hepatocellular carcinoma (HCC) was examined by in situ hybridization using a biotin-labeled recombinant, cloned HBV DNA probe. All patients tested were positive for both HBeAg and an...

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Detalles Bibliográficos
Autores principales: Lee, Dong Hoo, Lee, Jung Dal
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Association of Internal Medicine 1988
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4532137/
https://www.ncbi.nlm.nih.gov/pubmed/2856435
http://dx.doi.org/10.3904/kjim.1988.3.1.24
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author Lee, Dong Hoo
Lee, Jung Dal
author_facet Lee, Dong Hoo
Lee, Jung Dal
author_sort Lee, Dong Hoo
collection PubMed
description The distribution of hepatitis B virus (HBV) DNA in tumor tissue sections from six Korean patients with HBsAg positive hepatocellular carcinoma (HCC) was examined by in situ hybridization using a biotin-labeled recombinant, cloned HBV DNA probe. All patients tested were positive for both HBeAg and anti-HBc in their sera. HBV DNA was distributed abundantly in the cytoplasm and rarely in the nuclei of tumor cells. The validity of the in situ hybridization assay was confirmed by the dot blotting technique using a (32)P-labeled HBV DNA probe obtained by nick translation. In conclusion, it is speculated that integration of HBV DNA into host DNA as well as persistant amplified replication of the HBV DNA within the hepatocytes is linked etiologically to the development of human hepatocellular carcinoma.
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spelling pubmed-45321372015-10-02 Hepatitis B Virus DNA Detection by In Situ Hybridization in Human Hepatocellular Carcinoma Lee, Dong Hoo Lee, Jung Dal Korean J Intern Med Original Article The distribution of hepatitis B virus (HBV) DNA in tumor tissue sections from six Korean patients with HBsAg positive hepatocellular carcinoma (HCC) was examined by in situ hybridization using a biotin-labeled recombinant, cloned HBV DNA probe. All patients tested were positive for both HBeAg and anti-HBc in their sera. HBV DNA was distributed abundantly in the cytoplasm and rarely in the nuclei of tumor cells. The validity of the in situ hybridization assay was confirmed by the dot blotting technique using a (32)P-labeled HBV DNA probe obtained by nick translation. In conclusion, it is speculated that integration of HBV DNA into host DNA as well as persistant amplified replication of the HBV DNA within the hepatocytes is linked etiologically to the development of human hepatocellular carcinoma. Korean Association of Internal Medicine 1988-01 /pmc/articles/PMC4532137/ /pubmed/2856435 http://dx.doi.org/10.3904/kjim.1988.3.1.24 Text en Copyright © 1988 The Korean Association of Internal Medicine This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted noncommercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Lee, Dong Hoo
Lee, Jung Dal
Hepatitis B Virus DNA Detection by In Situ Hybridization in Human Hepatocellular Carcinoma
title Hepatitis B Virus DNA Detection by In Situ Hybridization in Human Hepatocellular Carcinoma
title_full Hepatitis B Virus DNA Detection by In Situ Hybridization in Human Hepatocellular Carcinoma
title_fullStr Hepatitis B Virus DNA Detection by In Situ Hybridization in Human Hepatocellular Carcinoma
title_full_unstemmed Hepatitis B Virus DNA Detection by In Situ Hybridization in Human Hepatocellular Carcinoma
title_short Hepatitis B Virus DNA Detection by In Situ Hybridization in Human Hepatocellular Carcinoma
title_sort hepatitis b virus dna detection by in situ hybridization in human hepatocellular carcinoma
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4532137/
https://www.ncbi.nlm.nih.gov/pubmed/2856435
http://dx.doi.org/10.3904/kjim.1988.3.1.24
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