DC Field | Value | Language |
---|---|---|
dc.contributor.author | S Lee | - |
dc.contributor.author | J Gang | - |
dc.contributor.author | S B Jeon | - |
dc.contributor.author | S H Choo | - |
dc.contributor.author | B Lee | - |
dc.contributor.author | Y G Kim | - |
dc.contributor.author | Y S Lee | - |
dc.contributor.author | J Jung | - |
dc.contributor.author | S Y Song | - |
dc.contributor.author | Sang Seok Koh | - |
dc.date.accessioned | 2017-04-19T09:08:18Z | - |
dc.date.available | 2017-04-19T09:08:18Z | - |
dc.date.issued | 2007 | - |
dc.identifier.issn | 0006-291X | - |
dc.identifier.uri | 10.1016/j.bbrc.2007.06.102 | ko |
dc.identifier.uri | https://oak.kribb.re.kr/handle/201005/8118 | - |
dc.description.abstract | We 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.publisher | Elsevier | - |
dc.title | Molecular cloning and functional analysis of a novel oncogene, cancer-upregulated gene 2 (CUG2) | - |
dc.title.alternative | Molecular cloning and functional analysis of a novel oncogene, cancer-upregulated gene 2 (CUG2) | - |
dc.type | Article | - |
dc.citation.title | Biochemical and Biophysical Research Communications | - |
dc.citation.number | 3 | - |
dc.citation.endPage | 639 | - |
dc.citation.startPage | 633 | - |
dc.citation.volume | 360 | - |
dc.contributor.affiliatedAuthor | Sang Seok Koh | - |
dc.contributor.alternativeName | 이수진 | - |
dc.contributor.alternativeName | 강진구 | - |
dc.contributor.alternativeName | 전순복 | - |
dc.contributor.alternativeName | 추승호 | - |
dc.contributor.alternativeName | 이복만 | - |
dc.contributor.alternativeName | 김영건 | - |
dc.contributor.alternativeName | 이양순 | - |
dc.contributor.alternativeName | 정진영 | - |
dc.contributor.alternativeName | 송시영 | - |
dc.contributor.alternativeName | 고상석 | - |
dc.identifier.bibliographicCitation | Biochemical and Biophysical Research Communications, vol. 360, no. 3, pp. 633-639 | - |
dc.identifier.doi | 10.1016/j.bbrc.2007.06.102 | - |
dc.subject.keyword | anti-cancer drug target | - |
dc.subject.keyword | cancer-upregulated gene 2 | - |
dc.subject.keyword | cloning | - |
dc.subject.keyword | microarray | - |
dc.subject.keyword | nuclear protein | - |
dc.subject.keyword | oncogene | - |
dc.subject.keyword | tumorigenesis | - |
dc.subject.local | anti-cancer drug target | - |
dc.subject.local | cancer-upregulated gene 2 | - |
dc.subject.local | Cloning | - |
dc.subject.local | clonning | - |
dc.subject.local | cloning | - |
dc.subject.local | microarray | - |
dc.subject.local | microarry | - |
dc.subject.local | Microarray | - |
dc.subject.local | microarrays | - |
dc.subject.local | nuclear protein | - |
dc.subject.local | Oncogene | - |
dc.subject.local | oncogene | - |
dc.subject.local | Oncogenes | - |
dc.subject.local | Tumorigenesis | - |
dc.subject.local | tumorigenesis | - |
dc.description.journalClass | Y | - |
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