Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/49668
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dc.contributor.authorPreeyanat Vongchanen_US
dc.contributor.authorSuchart Kothanen_US
dc.contributor.authorYupanan Wutti-Inen_US
dc.contributor.authorRobert J. Linhardten_US
dc.date.accessioned2018-09-04T04:05:13Z-
dc.date.available2018-09-04T04:05:13Z-
dc.date.issued2011-12-01en_US
dc.identifier.issn02507005en_US
dc.identifier.other2-s2.0-84855185404en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84855185404&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/49668-
dc.description.abstractHeparan sulfate proteoglycans (HSPGs) were isolated from normal human liver and a monoclonal antibody (MAb) was raised against them. Preliminary studies showed that MAb clone 1E4-1C2 was able to react with many cell lines tested, including hematopoietic cells and solid tumors. MAb1E4-1C2 was used to study whether HSPG was involved in growth and proliferation of human liver cancer using hepatocellular carcinoma (HCC) cell line (HepG2) as a model. Inhibition by MAb1E4-1C2 of HepG2 cell proliferation was studied in vitro by MTT assay. For in vivo assay, xenograft induction in athymic mice was performed. The results showed that MAb1E4-1C2 inhibited proliferation of HepG2 cells significantly, compared to isotype and medium control. MAb1E4-1C2 also suppressed the growth of tumor, resulting in smaller tumor size and weight. The investigation also showed that MAb1E4-1C2 inhibited proliferation and restricted tumor growth through the induction of apoptosis. The results suggest that HSPG might be involved in liver cancer cell proliferation. Therefore, a specific MAb that was raised against liver HSPG might be an alternative therapeutic agent for the treatment of human liver cancer.en_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.subjectMedicineen_US
dc.titleInhibition of human tumor xenograft growth in nude mice by a novel monoclonal anti-HSPG isolated from human liveren_US
dc.typeJournalen_US
article.title.sourcetitleAnticancer Researchen_US
article.volume31en_US
article.stream.affiliationsCMUen_US
article.stream.affiliationsChiang Mai Universityen_US
article.stream.affiliationsRensselaer Polytechnic Instituteen_US
Appears in Collections:CMUL: Journal Articles

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