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Inhibition of BET selectively eliminates undifferentiated pluripotent stem cells

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dc.contributor.authorIm, Jung Hyun-
dc.contributor.authorHwang, Seon In-
dc.contributor.authorKim, Jong-Wan-
dc.contributor.authorPark, Soon-Jung-
dc.contributor.authorKang, Kyu-ree-
dc.contributor.authorYou, Jueng Soo-
dc.contributor.authorKim, Kee Pyo-
dc.contributor.authorMoon, Sung-Hwan-
dc.contributor.authorCha, Hyuk-Jin-
dc.contributor.authorChung, Hyung-Min-
dc.contributor.authorSchoeler, Hans R.-
dc.contributor.authorHyun, Jung Keun-
dc.contributor.authorHan, Dong Wook-
dc.date.accessioned2024-01-09T03:31:23Z-
dc.date.available2024-01-09T03:31:23Z-
dc.date.issued2018-04-
dc.identifier.issn2095-9273-
dc.identifier.issn2095-9281-
dc.identifier.urihttps://scholarworks.bwise.kr/cau/handle/2019.sw.cau/69814-
dc.description.abstractEmbryonic stem cells (ESCs) maintain their cellular identity through the systematic regulation of master transcription factors and chromatin remodeling complexes. Recent work has shown that the unusually large-scale enhancers-namely super-enhancers (SEs), on which BRD4, a member of the bromodomain and extraterminal domain (BET) family is highly enriched-could regulate pluripotency-related transcription factors. Moreover, inhibition of BRD4 binding on SEs has been shown to induce the differentiation of ESCs. However, the underlying mechanism of BRD4 inhibition-mediated stem cell differentiation remains elusive. Here we show that both mouse and human ESCs lose their capacity for self-renewal upon treatment with JQ1, a selective inhibitor of BET family including BRD4, with rapid suppression of pluripotency-associated genes. Notably, a high concentration of JQ1 could selectively eliminate ESCs via apoptosis, without affecting the functionality of differentiated somatic cells from ESCs, suggesting that inhibition of BET may have a beneficial effect on the development of pluripotent stem cell-based cell therapy. (C) 2018 Science China Press. Published by Elsevier B.V. and Science China Press. All rights reserved.-
dc.format.extent11-
dc.language영어-
dc.language.isoENG-
dc.publisherSCIENCE PRESS-
dc.titleInhibition of BET selectively eliminates undifferentiated pluripotent stem cells-
dc.typeArticle-
dc.identifier.doi10.1016/j.scib.2018.02.023-
dc.identifier.bibliographicCitationSCIENCE BULLETIN, v.63, no.8, pp 477 - 487-
dc.description.isOpenAccessN-
dc.identifier.wosid000432524200005-
dc.identifier.scopusid2-s2.0-85044586236-
dc.citation.endPage487-
dc.citation.number8-
dc.citation.startPage477-
dc.citation.titleSCIENCE BULLETIN-
dc.citation.volume63-
dc.type.docTypeArticle-
dc.publisher.location중국-
dc.subject.keywordAuthorBromodomain and extraterminal domain (BET)-
dc.subject.keywordAuthorJQ1-
dc.subject.keywordAuthorPluripotent stem cells-
dc.subject.keywordPlusCYTOTOXIC ANTIBODY-
dc.subject.keywordPlusSUPER-ENHANCERS-
dc.subject.keywordPlusSELF-RENEWAL-
dc.subject.keywordPlusIDENTITY-
dc.subject.keywordPlusBRD4-
dc.subject.keywordPlusTUMORIGENICITY-
dc.subject.keywordPlusTRANSCRIPTION-
dc.subject.keywordPlusBROMODOMAINS-
dc.subject.keywordPlusFIBROBLASTS-
dc.subject.keywordPlusPRECURSORS-
dc.relation.journalResearchAreaScience & Technology - Other Topics-
dc.relation.journalWebOfScienceCategoryMultidisciplinary Sciences-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
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