Identification of intrahepatic cholangiocarcinoma related genes by comparison with normal liver tissues using expressed sequence tags

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dc.contributor.authorA G Wang-
dc.contributor.authorS Y Yoon-
dc.contributor.authorJ H Oh-
dc.contributor.authorYeo-Jin Jeon-
dc.contributor.authorMirang Kim-
dc.contributor.authorJ M Kim-
dc.contributor.authorSang-Soon Byun-
dc.contributor.authorJin Ok Yang-
dc.contributor.authorJ H Kim-
dc.contributor.authorD G Kim-
dc.contributor.authorYoung Il Yeom-
dc.contributor.authorHyang Sook Yoo-
dc.contributor.authorYong Sung Kim-
dc.contributor.authorNam-Soon Kim-
dc.date.accessioned2017-04-19T09:04:37Z-
dc.date.available2017-04-19T09:04:37Z-
dc.date.issued2006-
dc.identifier.issn0006-291X-
dc.identifier.uri10.1016/j.bbrc.2006.04.175ko
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/7430-
dc.description.abstractIntrahepatic cholangiocarcinoma (ICC), a malignant tumor derived from the bile duct epithelium, is one of the leading causes of death from cancer, worldwide. However, the mechanisms related to it remain largely unknown. In this study, an analysis of the gene expression profiles for ICC was done using the frequency of the ESTs obtained from nine cDNA libraries that constructed from 4 ICC cell lines and 4 normal liver tissues. One hundred and thirty-seven genes were identified as being either up- or down-regulated in human ICC cells. Thirty genes were randomly selected to confirm their differential expression in 4 human ICC cell lines and 5 ICC tissues compared to normal liver tissues by semi-quantitative RT-PCR. Among these genes, ANXA1, ANXA2, AMBP, and SERPINC1 were further verified by immunohistochemical analyses. In conclusion, these identified genes represent potential biomarkers for ICC and represent potential targets for elucidating the molecular mechanisms that are associated with ICC.-
dc.publisherElsevier-
dc.titleIdentification of intrahepatic cholangiocarcinoma related genes by comparison with normal liver tissues using expressed sequence tags-
dc.title.alternativeIdentification of intrahepatic cholangiocarcinoma related genes by comparison with normal liver tissues using expressed sequence tags-
dc.typeArticle-
dc.citation.titleBiochemical and Biophysical Research Communications-
dc.citation.number3-
dc.citation.endPage1032-
dc.citation.startPage1022-
dc.citation.volume345-
dc.contributor.affiliatedAuthorYeo-Jin Jeon-
dc.contributor.affiliatedAuthorMirang Kim-
dc.contributor.affiliatedAuthorSang-Soon Byun-
dc.contributor.affiliatedAuthorJin Ok Yang-
dc.contributor.affiliatedAuthorYoung Il Yeom-
dc.contributor.affiliatedAuthorHyang Sook Yoo-
dc.contributor.affiliatedAuthorYong Sung Kim-
dc.contributor.affiliatedAuthorNam-Soon Kim-
dc.contributor.alternativeNameWang-
dc.contributor.alternativeName윤선영-
dc.contributor.alternativeName오정화-
dc.contributor.alternativeName전여진-
dc.contributor.alternativeName김미랑-
dc.contributor.alternativeName김정민-
dc.contributor.alternativeName변상순-
dc.contributor.alternativeName양진옥-
dc.contributor.alternativeName김주헌-
dc.contributor.alternativeName김대건-
dc.contributor.alternativeName염영일-
dc.contributor.alternativeName유향숙-
dc.contributor.alternativeName김용성-
dc.contributor.alternativeName김남순-
dc.identifier.bibliographicCitationBiochemical and Biophysical Research Communications, vol. 345, no. 3, pp. 1022-1032-
dc.identifier.doi10.1016/j.bbrc.2006.04.175-
dc.subject.keywordESTs frequency-
dc.subject.keywordExpression profiling-
dc.subject.keywordIntrahepatic cholangiocarcinoma-
dc.subject.keywordLiver-
dc.subject.localESTs frequency-
dc.subject.localExpression profiling-
dc.subject.localIntrahepatic cholangiocarcinoma-
dc.subject.localIntrahepatic chol-angiocarcinoma-
dc.subject.localliver-
dc.subject.localLiver-
dc.subject.locallivers-
dc.description.journalClassY-
Appears in Collections:
Aging Convergence Research Center > 1. Journal Articles
Division of A.I. & Biomedical Research > Genomic Medicine Research Center > 1. Journal Articles
Division of A.I. & Biomedical Research > 1. Journal Articles
Division of A.I. & Biomedical Research > Orphan Disease Therapeutic Target Research Center > 1. Journal Articles
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