The cell adhesion molecule L1 promotes gallbladder carcinoma progression in vitro and in vivo = 담낭암 진행에서 L1CAM 기능 규명

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dc.contributor.authorJuyeon Jung-
dc.contributor.authorYeon Sung Son-
dc.contributor.authorH Park-
dc.contributor.authorSeong Kook Jeon-
dc.contributor.authorJ W Lee-
dc.contributor.authorS Y Choi-
dc.contributor.authorJ M Kim-
dc.contributor.authorY G Kwon-
dc.contributor.authorH J Hong-
dc.contributor.authorJeong Ki Min-
dc.date.accessioned2017-04-19T09:21:45Z-
dc.date.available2017-04-19T09:21:45Z-
dc.date.issued2011-
dc.identifier.issn1021-335X-
dc.identifier.uri10.3892/or.2011.1181ko
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/9999-
dc.description.abstractRecent studies have demonstrated that the cell adhesion molecule, L1, is expressed in several malignant tumor types and its expression correlates with tumor progression and metastasis. However, the role of L1 in gallbladder carcinoma (GBC) remains unclear. Here, we demonstrate that L1 is expressed in GBC cells and plays an important role in the growth, motility, invasiveness, and adhesiveness of GBC cells. Specific depletion or overexpression of L1 in the GBC cell lines JCRB1033 and SNU-308, respectively, was achieved by lentivirus-mediated transduction and expression of an L1 mRNA-specific short hairpin RNA or full-length human L1. Stable depletion of L1 led to a significant decrease in GBC cell proliferation, migration and invasion, as well as decreased intracellular signaling through AKT and FAK. Overexpression of L1 in GBC cells enhanced these cellular activities. In a GBC xenograft nude mouse model, suppression of L1 markedly reduced tumor growth and increased the survival of tumor-bearing mice whereas L1 overexpression stimulated tumorigenicity. Taken together, these results suggest that L1 plays a crucial role in GBC progression and may be a novel therapeutic target in GBC treatment.-
dc.publisherSpandidos Publ Ltd-
dc.titleThe cell adhesion molecule L1 promotes gallbladder carcinoma progression in vitro and in vivo = 담낭암 진행에서 L1CAM 기능 규명-
dc.title.alternativeThe cell adhesion molecule L1 promotes gallbladder carcinoma progression in vitro and in vivo-
dc.typeArticle-
dc.citation.titleOncology Reports-
dc.citation.number4-
dc.citation.endPage952-
dc.citation.startPage945-
dc.citation.volume25-
dc.contributor.affiliatedAuthorJuyeon Jung-
dc.contributor.affiliatedAuthorYeon Sung Son-
dc.contributor.affiliatedAuthorSeong Kook Jeon-
dc.contributor.affiliatedAuthorJeong Ki Min-
dc.contributor.alternativeName정주연-
dc.contributor.alternativeName손연성-
dc.contributor.alternativeName박홍렬-
dc.contributor.alternativeName전성국-
dc.contributor.alternativeName이중회-
dc.contributor.alternativeName최송이-
dc.contributor.alternativeName김진만-
dc.contributor.alternativeName권영근-
dc.contributor.alternativeName홍효정-
dc.contributor.alternativeName민정기-
dc.identifier.bibliographicCitationOncology Reports, vol. 25, no. 4, pp. 945-952-
dc.identifier.doi10.3892/or.2011.1181-
dc.subject.keywordGallbladder carcinoma-
dc.subject.keywordL1 cell adhesion molecule-
dc.subject.keywordTherapeutic target-
dc.subject.keywordTumor progression-
dc.subject.localGallbladder carcinoma-
dc.subject.localL1 cell adhesion molecule-
dc.subject.localTherapeutic Targets-
dc.subject.localtherapeutic target-
dc.subject.localtherapeutic targets-
dc.subject.localTherapeutic target-
dc.subject.localTherapeutic targets-
dc.subject.localtumor progression-
dc.subject.localTumor progression-
dc.subject.localTumor Progression-
dc.description.journalClassY-
Appears in Collections:
Division of Research on National Challenges > Bionanotechnology Research Center > 1. Journal Articles
Division of Biomedical Research > Biotherapeutics Translational Research Center > 1. Journal Articles
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