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Roles and epigenetic regulation of epithelial-mesenchymal transition and its transcription factors in cancer initiation and progression

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dc.contributor.authorLee, Jeong-Yeon-
dc.contributor.authorKong, Gu-
dc.date.accessioned2022-07-14T23:57:04Z-
dc.date.available2022-07-14T23:57:04Z-
dc.date.created2021-05-12-
dc.date.issued2016-12-
dc.identifier.issn1420-682X-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/153414-
dc.description.abstractThe epithelial-mesenchymal transition (EMT) is a crucial developmental process by which epithelial cells undergo a mesenchymal phenotypic change. During EMT, epigenetic mechanisms including DNA methylation and histone modifications are involved in the regulation of EMT-related genes. The epigenetic gene silencing of the epithelial marker E-cadherin has been well characterized. In particular, three major transcriptional repressors of E-cadherin, Snail, ZEB, and Twist families, also known as EMT-inducing transcription factors (EMT-TFs), play a crucial role in this process by cooperating with multiple epigenetic modifiers. Furthermore, recent studies have identified the novel epigenetic modifiers that control the expression of EMT-TFs, and these modifiers have emerged as critical regulators of cancer development and as novel therapeutic targets for human cancer. In this review, the diverse functions of EMT-TFs in cancer progression, the cooperative mechanisms of EMT-TFs with epigenetic modifiers, and epigenetic regulatory roles for the expression of EMT-TFs will be discussed.-
dc.language영어-
dc.language.isoen-
dc.publisherSPRINGER BASEL AG-
dc.titleRoles and epigenetic regulation of epithelial-mesenchymal transition and its transcription factors in cancer initiation and progression-
dc.typeArticle-
dc.contributor.affiliatedAuthorLee, Jeong-Yeon-
dc.contributor.affiliatedAuthorKong, Gu-
dc.identifier.doi10.1007/s00018-016-2313-z-
dc.identifier.scopusid2-s2.0-84979703525-
dc.identifier.wosid000387491800006-
dc.identifier.bibliographicCitationCELLULAR AND MOLECULAR LIFE SCIENCES, v.73, no.24, pp.4643 - 4660-
dc.relation.isPartOfCELLULAR AND MOLECULAR LIFE SCIENCES-
dc.citation.titleCELLULAR AND MOLECULAR LIFE SCIENCES-
dc.citation.volume73-
dc.citation.number24-
dc.citation.startPage4643-
dc.citation.endPage4660-
dc.type.rimsART-
dc.type.docTypeReview-
dc.description.journalClass1-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaCell Biology-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryCell Biology-
dc.subject.keywordPlusGROWTH-FACTOR RECEPTOR-
dc.subject.keywordPlusE-CADHERIN EXPRESSION-
dc.subject.keywordPlusHYPOXIA-INDUCIBLE FACTOR-1-ALPHA-
dc.subject.keywordPlusREPRESSES E-CADHERIN-
dc.subject.keywordPlusSQUAMOUS-CELL CARCINOMA-
dc.subject.keywordPlusBREAST-CANCER-
dc.subject.keywordPlusSTEM-CELLS-
dc.subject.keywordPlusHISTONE DEMETHYLASE-
dc.subject.keywordPlusDNA METHYLATION-
dc.subject.keywordPlusUP-REGULATION-
dc.subject.keywordAuthorEMT-
dc.subject.keywordAuthorEMT transcription factor-
dc.subject.keywordAuthorHuman cancer-
dc.subject.keywordAuthorEpigenetics-
dc.subject.keywordAuthorChromatin-
dc.subject.keywordAuthorHistone modification-
dc.subject.keywordAuthorDNA methylation-
dc.identifier.urlhttps://link.springer.com/article/10.1007%2Fs00018-016-2313-z-
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