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- Publisher Website: 10.1038/bjc.1986.153
- Scopus: eid_2-s2.0-0022591802
- PMID: 3015183
- WOS: WOS:A1986D141000009
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Article: Serum hepatitis B viral DNA in HBsAg-positive hepatocellular carcinoma treated with interferon or adriamycin
Title | Serum hepatitis B viral DNA in HBsAg-positive hepatocellular carcinoma treated with interferon or adriamycin |
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Authors | |
Issue Date | 1986 |
Publisher | Nature Publishing Group. The Journal's web site is located at http://www.nature.com/bjc |
Citation | British Journal Of Cancer, 1986, v. 54 n. 1, p. 67-73 How to Cite? |
Abstract | Sera from 31 HBsAg-positive Chinese patients with inoperable hepatocellular carcinoma (HCC) were tested for hepatitis B virus DNA (HBV DNA) by means of dot hybridisation and Southern blot technique. HBV DNA probes were prepared from human plasma. Eighteen of the patients were HBeAb-positive, 12 were HBeAg-positive and one case had neither marker. Serial specimens were obtained from 16 cases over 5-42 weeks, while the patients were treated with recombinant leukocyte A interferom (rIFN-A) or adriamycin. Seven patients (2 HBeAg-positive, 5 HBeAb-positive) were positive for HBV DNA. In two patients HBV DNA and HBV DNA polymerase (DNAp) appeared in serum weeks after rIFN-A or adriamycin treatment was started. In two other cases, HBV DNA that was initially present disappeared during rIFN-A treatment. In a fifth patient HBV DNA persisting after adriamycin treatment diminished after change of treatment to rIFN-A. With one possible exception the HBV DNA detectable by Southern blot technique was composed chiefly of sequences 2.2-3.2 kb size indicating the presence of unintegrated DNA forms. DNAp activities were raised in the presence of HBV DNA in 4 patients. These findings show that HBV replication can be activated or suppressed in advanced HCC. Treatment with rIFN-A may have been effective in suppressing HBV DNA synthesis, but the number of cases studied was too small to arrive at a definite conclusion on this point. |
Persistent Identifier | http://hdl.handle.net/10722/161705 |
ISSN | 2023 Impact Factor: 6.4 2023 SCImago Journal Rankings: 3.000 |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Lin, HJ | en_US |
dc.contributor.author | Lai, CL | en_US |
dc.contributor.author | Wu, PC | en_US |
dc.date.accessioned | 2012-09-05T05:14:12Z | - |
dc.date.available | 2012-09-05T05:14:12Z | - |
dc.date.issued | 1986 | en_US |
dc.identifier.citation | British Journal Of Cancer, 1986, v. 54 n. 1, p. 67-73 | en_US |
dc.identifier.issn | 0007-0920 | en_US |
dc.identifier.uri | http://hdl.handle.net/10722/161705 | - |
dc.description.abstract | Sera from 31 HBsAg-positive Chinese patients with inoperable hepatocellular carcinoma (HCC) were tested for hepatitis B virus DNA (HBV DNA) by means of dot hybridisation and Southern blot technique. HBV DNA probes were prepared from human plasma. Eighteen of the patients were HBeAb-positive, 12 were HBeAg-positive and one case had neither marker. Serial specimens were obtained from 16 cases over 5-42 weeks, while the patients were treated with recombinant leukocyte A interferom (rIFN-A) or adriamycin. Seven patients (2 HBeAg-positive, 5 HBeAb-positive) were positive for HBV DNA. In two patients HBV DNA and HBV DNA polymerase (DNAp) appeared in serum weeks after rIFN-A or adriamycin treatment was started. In two other cases, HBV DNA that was initially present disappeared during rIFN-A treatment. In a fifth patient HBV DNA persisting after adriamycin treatment diminished after change of treatment to rIFN-A. With one possible exception the HBV DNA detectable by Southern blot technique was composed chiefly of sequences 2.2-3.2 kb size indicating the presence of unintegrated DNA forms. DNAp activities were raised in the presence of HBV DNA in 4 patients. These findings show that HBV replication can be activated or suppressed in advanced HCC. Treatment with rIFN-A may have been effective in suppressing HBV DNA synthesis, but the number of cases studied was too small to arrive at a definite conclusion on this point. | en_US |
dc.language | eng | en_US |
dc.publisher | Nature Publishing Group. The Journal's web site is located at http://www.nature.com/bjc | en_US |
dc.relation.ispartof | British Journal of Cancer | en_US |
dc.subject.mesh | Aged | en_US |
dc.subject.mesh | Base Sequence | en_US |
dc.subject.mesh | Carcinoma, Hepatocellular - Blood - Drug Therapy | en_US |
dc.subject.mesh | Dna, Viral - Metabolism | en_US |
dc.subject.mesh | Doxorubicin - Therapeutic Use | en_US |
dc.subject.mesh | Electrophoresis, Agar Gel | en_US |
dc.subject.mesh | Hepatitis B Surface Antigens - Analysis | en_US |
dc.subject.mesh | Hepatitis B Virus - Metabolism | en_US |
dc.subject.mesh | Humans | en_US |
dc.subject.mesh | Interferon Type I - Therapeutic Use | en_US |
dc.subject.mesh | Liver Neoplasms - Blood - Drug Therapy | en_US |
dc.subject.mesh | Nucleic Acid Hybridization | en_US |
dc.title | Serum hepatitis B viral DNA in HBsAg-positive hepatocellular carcinoma treated with interferon or adriamycin | en_US |
dc.type | Article | en_US |
dc.identifier.email | Lai, CL:hrmelcl@hku.hk | en_US |
dc.identifier.authority | Lai, CL=rp00314 | en_US |
dc.description.nature | link_to_subscribed_fulltext | en_US |
dc.identifier.doi | 10.1038/bjc.1986.153 | - |
dc.identifier.pmid | 3015183 | - |
dc.identifier.scopus | eid_2-s2.0-0022591802 | en_US |
dc.identifier.volume | 54 | en_US |
dc.identifier.issue | 1 | en_US |
dc.identifier.spage | 67 | en_US |
dc.identifier.epage | 73 | en_US |
dc.identifier.isi | WOS:A1986D141000009 | - |
dc.publisher.place | United Kingdom | en_US |
dc.identifier.scopusauthorid | Lin, HJ=7405571292 | en_US |
dc.identifier.scopusauthorid | Lai, CL=7403086396 | en_US |
dc.identifier.scopusauthorid | Wu, PC=7403119323 | en_US |
dc.identifier.issnl | 0007-0920 | - |