Molecular cloning and functional analysis of a novel oncogene, cancer-upregulated gene 2 (CUG2)

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dc.contributor.authorS Lee-
dc.contributor.authorJ Gang-
dc.contributor.authorS B Jeon-
dc.contributor.authorS H Choo-
dc.contributor.authorB Lee-
dc.contributor.authorY G Kim-
dc.contributor.authorY S Lee-
dc.contributor.authorJ Jung-
dc.contributor.authorS Y Song-
dc.contributor.authorSang Seok Koh-
dc.date.accessioned2017-04-19T09:08:18Z-
dc.date.available2017-04-19T09:08:18Z-
dc.date.issued2007-
dc.identifier.issn0006-291X-
dc.identifier.uri10.1016/j.bbrc.2007.06.102ko
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/8118-
dc.description.abstractWe examined genome-wide differences in gene expression between tumor biopsies and normal tissues in order to identify differentially regulated genes in tumors. Cancer-upregulated gene 2 (CUG2) was identified as an expressed sequence tag (EST) that exhibits significant differential expression in multiple human cancer types. CUG2 showed weak sequence homology with the down-regulator of transcription 1 (DR1) gene, a human transcription repressor. We found that EGFP-CUG2 fusion proteins were predominantly localized in the nucleus, suggesting their putative role in gene regulation. In addition, CUG2-overexpressing mouse fibroblast cells exhibited distinct cancer-specific phenotypes in vitro and developed into tumors in nude mice. Taken together, these findings suggest that CUG2 is a novel tumor-associated gene that is commonly activated in various human cancers and exhibits high transforming activities; it possibly belongs to a transcription regulator family that is involved in tumor biogenesis.-
dc.publisherElsevier-
dc.titleMolecular cloning and functional analysis of a novel oncogene, cancer-upregulated gene 2 (CUG2)-
dc.title.alternativeMolecular cloning and functional analysis of a novel oncogene, cancer-upregulated gene 2 (CUG2)-
dc.typeArticle-
dc.citation.titleBiochemical and Biophysical Research Communications-
dc.citation.number3-
dc.citation.endPage639-
dc.citation.startPage633-
dc.citation.volume360-
dc.contributor.affiliatedAuthorSang Seok Koh-
dc.contributor.alternativeName이수진-
dc.contributor.alternativeName강진구-
dc.contributor.alternativeName전순복-
dc.contributor.alternativeName추승호-
dc.contributor.alternativeName이복만-
dc.contributor.alternativeName김영건-
dc.contributor.alternativeName이양순-
dc.contributor.alternativeName정진영-
dc.contributor.alternativeName송시영-
dc.contributor.alternativeName고상석-
dc.identifier.bibliographicCitationBiochemical and Biophysical Research Communications, vol. 360, no. 3, pp. 633-639-
dc.identifier.doi10.1016/j.bbrc.2007.06.102-
dc.subject.keywordanti-cancer drug target-
dc.subject.keywordcancer-upregulated gene 2-
dc.subject.keywordcloning-
dc.subject.keywordmicroarray-
dc.subject.keywordnuclear protein-
dc.subject.keywordoncogene-
dc.subject.keywordtumorigenesis-
dc.subject.localanti-cancer drug target-
dc.subject.localcancer-upregulated gene 2-
dc.subject.localCloning-
dc.subject.localclonning-
dc.subject.localcloning-
dc.subject.localmicroarray-
dc.subject.localmicroarry-
dc.subject.localMicroarray-
dc.subject.localmicroarrays-
dc.subject.localnuclear protein-
dc.subject.localOncogene-
dc.subject.localoncogene-
dc.subject.localOncogenes-
dc.subject.localTumorigenesis-
dc.subject.localtumorigenesis-
dc.description.journalClassY-
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