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Kazinol C from Broussonetia kazinoki activates AMP-activated protein kinase to induce antitumorigenic effects in HT-29 colon cancer cells

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dc.contributor.authorKim, Hak-Su-
dc.contributor.authorLim, Jihyun-
dc.contributor.authorLee, Da Yeon-
dc.contributor.authorRyu, Jae-Ha-
dc.contributor.authorLim, Jong-Seok-
dc.date.available2021-02-22T11:46:24Z-
dc.date.issued2015-01-
dc.identifier.issn1021-335X-
dc.identifier.issn1791-2431-
dc.identifier.urihttps://scholarworks.sookmyung.ac.kr/handle/2020.sw.sookmyung/10704-
dc.description.abstractKazinol C is a 1,3-diphenylpropane, obtained from Broussonetia kazinoki, that has been employed in folk medicine as an edema suppressant. It exerts beneficial effects in oxidative stress-related diseases, such as cancer. However, the molecular mechanism involved in the anticancer effects remains to be determined. AMP-activated protein kinase (AMPK) has emerged as a possible anticancer target molecule. The present study investigated the effect of kazinol C on AMPK activation as well as subsequent HT-29 colon cancer cell viability, apoptosis and migration. Kazinol C markedly induced AMPK phosphorylation and significantly attenuated HT-29 colon cancer cell growth and viability. Compound C, as a well-known AMPK inhibitor, blocked the kazinol C-induced cell death, and stable transduction of dominant-negative (DN) AMPK in colon cancer cells also inhibited kazinol C-induced cell apoptosis. In addition, kazinol C inhibited HT-29 cell migration and anchorage-independent growth. AMPK inhibition using stable transduction with DN AMPK significantly abrogated the kazinol C-induced inhibition of cancer cell migration. Thus, AMPK is a critical and novel regulator of kazinol C-mediated cancer cell apoptosis and inhibition of migration, suggesting that AMPK is a prime cancer target.-
dc.format.extent7-
dc.language영어-
dc.language.isoENG-
dc.publisherSPANDIDOS PUBL LTD-
dc.titleKazinol C from Broussonetia kazinoki activates AMP-activated protein kinase to induce antitumorigenic effects in HT-29 colon cancer cells-
dc.typeArticle-
dc.publisher.location그리이스-
dc.identifier.doi10.3892/or.2014.3601-
dc.identifier.scopusid2-s2.0-84916212079-
dc.identifier.wosid000346636200029-
dc.identifier.bibliographicCitationONCOLOGY REPORTS, v.33, no.1, pp 223 - 229-
dc.citation.titleONCOLOGY REPORTS-
dc.citation.volume33-
dc.citation.number1-
dc.citation.startPage223-
dc.citation.endPage229-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaOncology-
dc.relation.journalWebOfScienceCategoryOncology-
dc.subject.keywordPlusISOPRENYLATED FLAVANS-
dc.subject.keywordPlusMIGRATION-
dc.subject.keywordPlusMETABOLISM-
dc.subject.keywordPlusEXPRESSION-
dc.subject.keywordPlusAPOPTOSIS-
dc.subject.keywordPlusPATHWAY-
dc.subject.keywordPlusGROWTH-
dc.subject.keywordPlusPHOSPHORYLATION-
dc.subject.keywordPlusINHIBITION-
dc.subject.keywordPlusQUERCETIN-
dc.subject.keywordAuthorkazinol C-
dc.subject.keywordAuthorAMP-activated protein kinase-
dc.subject.keywordAuthorapoptosis-
dc.subject.keywordAuthormigration-
dc.subject.keywordAuthorcolon cancer-
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