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dc.contributor.author박상희*
dc.contributor.author조성엽*
dc.date.accessioned2018-12-14T16:31:05Z-
dc.date.available2018-12-14T16:31:05Z-
dc.date.issued2018*
dc.identifier.issn0006-4971*
dc.identifier.otherOAK-22503*
dc.identifier.urihttps://dspace.ewha.ac.kr/handle/2015.oak/247803-
dc.description.abstractEpstein-Barr virus (EBV)-positive diffuse large B-cell lymphomas (EBV1-DLBLs) tend to occur in immunocompromised patients, such as the elderly or those undergoing solid organ transplantation. The pathogenesis and genomic characteristics of EBV1-DLBLs are largely unknown because of the limited availability of human samples and lack of experimental animal models. We observed the development of 25 human EBV1-DLBLs during the engraftment of gastric adenocarcinomas into immunodeficient mice. An integrated genomic analysis of the human-derived EBV1-DLBLs revealed enrichment of mutations in Rho pathway genes, including RHPN2, and Rho pathway transcriptomic activation. Targeting the Rho pathway using a Rho-associated protein kinase (ROCK) inhibitor, fasudil, markedly decreased tumor growth in EBV1-DLBL patient-derived xenograft (PDX) models. Thus, alterations in the Rho pathway appear to contribute to EBV-induced lymphomagenesis in immunosuppressed environments. © 2018 by The American Society of Hematology.*
dc.description.sponsorshipMinistry of Science, ICT and Future Planning*
dc.languageEnglish*
dc.publisherAmerican Society of Hematology*
dc.titleAlterations in the Rho pathway contribute to Epstein-Barr virus–induced lymphomagenesis in immunosuppressed environments*
dc.typeArticle*
dc.relation.issue17*
dc.relation.volume131*
dc.relation.indexSCIE*
dc.relation.indexSCOPUS*
dc.relation.startpage1931*
dc.relation.lastpage1941*
dc.relation.journaltitleBlood*
dc.identifier.doi10.1182/blood-2017-07-797209*
dc.identifier.wosidWOS:000431101100010*
dc.identifier.scopusid2-s2.0-85047871272*
dc.author.googleCho S.-Y.*
dc.author.googleSung C.O.*
dc.author.googleChae J.*
dc.author.googleLee J.*
dc.author.googleNa D.*
dc.author.googleKang W.*
dc.author.googleKang J.*
dc.author.googleMin S.*
dc.author.googleLee A.*
dc.author.googleKwak E.*
dc.author.googleKim J.*
dc.author.googleChoi B.*
dc.author.googleKim H.*
dc.author.googleChuang J.H.*
dc.author.googlePak H.-K.*
dc.author.googlePark C.-S.*
dc.author.googlePark S.*
dc.author.googleKo Y.H.*
dc.author.googleLee D.*
dc.author.googleRoh J.*
dc.author.googleCho M.-S.*
dc.author.googleJu Y.S.*
dc.author.googleSuh Y.-S.*
dc.author.googleKong S.-H.*
dc.author.googleLee H.-J.*
dc.author.googleKeck J.*
dc.author.googleBanchereau J.*
dc.author.googleLiu E.T.*
dc.author.googleKim W.-H.*
dc.author.googlePark H.*
dc.author.googleYang H.-K.*
dc.author.googleKim J.-I.*
dc.author.googleLee C.*
dc.contributor.scopusid박상희(12041890800)*
dc.contributor.scopusid조성엽(7404884433)*
dc.date.modifydate20240220112152*
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의과대학 > 의학과 > Journal papers
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