PRDM1, a tumor-suppressor gene, is induced by Genkwadaphnin in human colon cancer SW620 cells

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dc.contributor.authorHo Bum Kang-
dc.contributor.authorHa Reum Lee-
dc.contributor.authorDa Jung Jee-
dc.contributor.authorSu Hyun Shin-
dc.contributor.authorS S Nah-
dc.contributor.authorS Y Yoon-
dc.contributor.authorJae Wha Kim-
dc.date.accessioned2017-04-19T10:16:35Z-
dc.date.available2017-04-19T10:16:35Z-
dc.date.issued2016-
dc.identifier.issn0730-2312-
dc.identifier.uri10.1002/jcb.25262ko
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/13095-
dc.description.abstractGenkwadaphnin (GD-1) is isolated from the flower buds of Daphne genkwa Siebold et Zuccarini (Thymelaeaceae), and it has been used as a traditional Korean and Chinese medicine. In this study, the authors observe that GD-1 inhibits the growth of the colon cancer cell line, SW620, through the up-regulation of p21 expression in a PRDM1-dependent manner. After treatment with GD-1, the transcriptional repressor PRDM1 is prominently induced in SW620 cells. Furthermore, GD-1 induce the phosphorylation of PKD1 and MEK and subsequently provide PRDM1 enhancement, resulting in the suppression of c-Myc expression and the up-regulation of p21. PKD1 knockdown using siRNA abrogates PRDM1 expression by GD-1 and subsequently disrupts the regulation of c-Myc and p21 expression. Treating SW620 cells with GD-1 inhibits cell-cycle progression and is characterized by the down-regulation of c-Myc followed by the up-regulation of p21 expression. The up-regulation of p21 by GD-1 induces the growth arrest of the SW620 colon cancer cell line. Based on these data, the authors propose that GD-1 has tumor-suppressor activity that may contribute to the anti-tumor effects of PRDM1 in colon cancer.-
dc.publisherWiley-
dc.titlePRDM1, a tumor-suppressor gene, is induced by Genkwadaphnin in human colon cancer SW620 cells-
dc.title.alternativePRDM1, a tumor-suppressor gene, is induced by Genkwadaphnin in human colon cancer SW620 cells-
dc.typeArticle-
dc.citation.titleJournal of Cellular Biochemistry-
dc.citation.number1-
dc.citation.endPage179-
dc.citation.startPage172-
dc.citation.volume117-
dc.contributor.affiliatedAuthorHo Bum Kang-
dc.contributor.affiliatedAuthorHa Reum Lee-
dc.contributor.affiliatedAuthorDa Jung Jee-
dc.contributor.affiliatedAuthorSu Hyun Shin-
dc.contributor.affiliatedAuthorJae Wha Kim-
dc.contributor.alternativeName강호범-
dc.contributor.alternativeName이하름-
dc.contributor.alternativeName지다정-
dc.contributor.alternativeName신수현-
dc.contributor.alternativeName나성수-
dc.contributor.alternativeName윤선영-
dc.contributor.alternativeName김재화-
dc.identifier.bibliographicCitationJournal of Cellular Biochemistry, vol. 117, no. 1, pp. 172-179-
dc.identifier.doi10.1002/jcb.25262-
dc.subject.keywordGENKWADAPHNIN (GD-1)-
dc.subject.keywordPKD1-
dc.subject.keywordPRDM1-
dc.subject.localGENKWADAPHNIN (GD-1)-
dc.subject.localGenkwadaphnin-
dc.subject.localgenkwadaphnin-
dc.subject.localPKD1-
dc.subject.localPRDM1-
dc.description.journalClassY-
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Division of A.I. & Biomedical Research > Immunotherapy Research Center > 1. Journal Articles
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