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The roles of TRIO and F-actin-binding protein in glioblastoma cells

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dc.contributor.authorLee, Hyunji-
dc.contributor.authorKim, Minhee-
dc.contributor.authorPark, Jisoo-
dc.contributor.authorTran, Quangdon-
dc.contributor.authorHong, Youngeun-
dc.contributor.authorCho, Hyeonjeong-
dc.contributor.authorPark, Sungjin-
dc.contributor.authorHong, Suntaek-
dc.contributor.authorBrazil, Derek P.-
dc.contributor.authorKim, Seon-Hwan-
dc.contributor.authorPark, Jongsun-
dc.date.available2020-02-27T11:42:01Z-
dc.date.created2020-02-06-
dc.date.issued2018-03-
dc.identifier.issn1791-2997-
dc.identifier.urihttps://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/4016-
dc.description.abstractTRIO and F-actin-binding protein (TrioBP), which was initially discovered as a binding partner of Trio and F-actin, is a critical factor associated with hearing loss in humans. However, the function of TrioBP in cancer has not been investigated. In the present study, TrioBP expression was indicated to be highly elevated in U87-MG and U343-MG cells. Furthermore, the TrioBP mRNA expression level was markedly increased in U87-MG and U251-MG cells compared with that in cerebral cortex cells, as determined by deep sequencing. Comprehensive analysis of a public TCGA dataset confirmed that TrioBP expression is elevated in patients with glioblastoma. In summary, the present data indicate that TrioBP expression is increased in glioblastoma cell lines and in patients with glioma, suggesting that TrioBP has potential as a diagnostic marker or therapeutic agent for glioma.-
dc.language영어-
dc.language.isoen-
dc.publisherSPANDIDOS PUBL LTD-
dc.relation.isPartOfMOLECULAR MEDICINE REPORTS-
dc.subjectNEWLY-DIAGNOSED GLIOBLASTOMA-
dc.subjectNUCLEOTIDE EXCHANGE FACTOR-
dc.subjectHEARING-LOSS-
dc.subjectANGIOGENESIS-
dc.subjectBEVACIZUMAB-
dc.subjectMUTATIONS-
dc.subjectENCODES-
dc.titleThe roles of TRIO and F-actin-binding protein in glioblastoma cells-
dc.typeArticle-
dc.type.rimsART-
dc.description.journalClass1-
dc.identifier.wosid000424400000140-
dc.identifier.doi10.3892/mmr.2018.8458-
dc.identifier.bibliographicCitationMOLECULAR MEDICINE REPORTS, v.17, no.3, pp.4540 - 4546-
dc.identifier.scopusid2-s2.0-85041174482-
dc.citation.endPage4546-
dc.citation.startPage4540-
dc.citation.titleMOLECULAR MEDICINE REPORTS-
dc.citation.volume17-
dc.citation.number3-
dc.contributor.affiliatedAuthorHong, Suntaek-
dc.type.docTypeArticle-
dc.subject.keywordAuthorTrioBP-
dc.subject.keywordAuthorcytoskeleton-
dc.subject.keywordAuthorglioma-
dc.subject.keywordAuthorbiomarker-
dc.subject.keywordPlusNEWLY-DIAGNOSED GLIOBLASTOMA-
dc.subject.keywordPlusNUCLEOTIDE EXCHANGE FACTOR-
dc.subject.keywordPlusHEARING-LOSS-
dc.subject.keywordPlusANGIOGENESIS-
dc.subject.keywordPlusBEVACIZUMAB-
dc.subject.keywordPlusMUTATIONS-
dc.subject.keywordPlusENCODES-
dc.relation.journalResearchAreaOncology-
dc.relation.journalResearchAreaResearch & Experimental Medicine-
dc.relation.journalWebOfScienceCategoryOncology-
dc.relation.journalWebOfScienceCategoryMedicine, Research & Experimental-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
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