DC Field | Value | Language |
---|---|---|
dc.contributor.author | Kim, Jayoung | ko |
dc.contributor.author | Hong, Chae Mi | ko |
dc.contributor.author | Park, Su Min | ko |
dc.contributor.author | Shin, Dong Hoon | ko |
dc.contributor.author | Kim, Jee Yeon | ko |
dc.contributor.author | Kwon, Sang-Mo | ko |
dc.contributor.author | Kim, Jae Ho | ko |
dc.contributor.author | Kim, Chi Dae | ko |
dc.contributor.author | Lim, Dae-Sik | ko |
dc.contributor.author | Lee, Dongjun | ko |
dc.date.accessioned | 2018-07-24T02:57:22Z | - |
dc.date.available | 2018-07-24T02:57:22Z | - |
dc.date.created | 2018-07-16 | - |
dc.date.created | 2018-07-16 | - |
dc.date.created | 2018-07-16 | - |
dc.date.issued | 2018-07 | - |
dc.identifier.citation | BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, v.502, no.1, pp.43 - 47 | - |
dc.identifier.issn | 0006-291X | - |
dc.identifier.uri | http://hdl.handle.net/10203/244532 | - |
dc.description.abstract | SURF4, which is located in the Surfeit gene cluster, encodes for a conserved integral membrane protein containing multiple putative transmembrane regions. However, the physiological role of SURF4 has not been determined. We found that SURF4 demonstrated aberrant amplification and increased expression in the tumor tissues of several human cancer patients. Overexpression of SURF4 led to increased cell proliferation, migration, and maintenance of anchorage-independent growth. In addition, NIH3T3 cells overexpressing SURF4 induced tumor growth in the mice. Collectively, our findings demonstrate that SURF4 has the potential for inducing cellular transformation and cell migration in vitro and has oncogenic transformation ability in vivo. (C) 2018 The Authors. Published by Elsevier Inc. | - |
dc.language | English | - |
dc.publisher | ACADEMIC PRESS INC ELSEVIER SCIENCE | - |
dc.title | SURF4 has oncogenic potential in NIH3T3 cells | - |
dc.type | Article | - |
dc.identifier.wosid | 000436383800006 | - |
dc.identifier.scopusid | 2-s2.0-85047070631 | - |
dc.type.rims | ART | - |
dc.citation.volume | 502 | - |
dc.citation.issue | 1 | - |
dc.citation.beginningpage | 43 | - |
dc.citation.endingpage | 47 | - |
dc.citation.publicationname | BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS | - |
dc.identifier.doi | 10.1016/j.bbrc.2018.05.116 | - |
dc.contributor.localauthor | Lim, Dae-Sik | - |
dc.contributor.nonIdAuthor | Kim, Jayoung | - |
dc.contributor.nonIdAuthor | Hong, Chae Mi | - |
dc.contributor.nonIdAuthor | Park, Su Min | - |
dc.contributor.nonIdAuthor | Shin, Dong Hoon | - |
dc.contributor.nonIdAuthor | Kim, Jee Yeon | - |
dc.contributor.nonIdAuthor | Kwon, Sang-Mo | - |
dc.contributor.nonIdAuthor | Kim, Jae Ho | - |
dc.contributor.nonIdAuthor | Kim, Chi Dae | - |
dc.description.isOpenAccess | Y | - |
dc.type.journalArticle | Article | - |
dc.subject.keywordAuthor | SURF4 | - |
dc.subject.keywordAuthor | Oncogene | - |
dc.subject.keywordAuthor | Tumor formation | - |
dc.subject.keywordAuthor | Cellular transformation | - |
dc.subject.keywordAuthor | Cell migration | - |
dc.subject.keywordAuthor | Oncogenic transformation | - |
dc.subject.keywordPlus | GENE-EXPRESSION SIGNATURE | - |
dc.subject.keywordPlus | TUMOR-SUPPRESSOR RASSF1A | - |
dc.subject.keywordPlus | LOCUS CONTAINS | - |
dc.subject.keywordPlus | COMPLEX | - |
dc.subject.keywordPlus | CANCER | - |
dc.subject.keywordPlus | TRANSPORT | - |
dc.subject.keywordPlus | APC-CDC20 | - |
dc.subject.keywordPlus | LYMPHOMAS | - |
dc.subject.keywordPlus | VESICLES | - |
dc.subject.keywordPlus | INSIGHTS | - |
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