Butein is a novel anti-adipogenic compound

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dc.contributor.authorN J Song-
dc.contributor.authorH J Yoon-
dc.contributor.authorK H Kim-
dc.contributor.authorS R Jung-
dc.contributor.authorW S Jang-
dc.contributor.authorC R Seo-
dc.contributor.authorY M Lee-
dc.contributor.authorD H Kweon-
dc.contributor.authorJ W Hong-
dc.contributor.authorJeong Soo Lee-
dc.contributor.authorK M Park-
dc.contributor.authorK R Lee-
dc.contributor.authorK W Park-
dc.date.accessioned2017-04-19T09:46:14Z-
dc.date.available2017-04-19T09:46:14Z-
dc.date.issued2013-
dc.identifier.issn0022-2275-
dc.identifier.uri10.1194/jlr.M035576ko
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/11648-
dc.description.abstractRhus verniciflua Stokes (RVS) has been used as a traditional herbal medicine for its various biological activities including anti-adipogenic effects. Activity-guided separation led to the identification of the anti-adipogenic functions of butein. Butein, a novel anti-adipogenic compound, robustly suppressed lipid accumulation and inhibited expression of adipogenic markers. Molecular studies showed that activated transforming growth factor- β (TGF- β ) and suppressed signal transducer and activator of transcription 3 (STAT3) signaling pathways were mediated by butein. Analysis of the temporal expression profiles suggests that TGF- β signaling precedes the STAT3 in the butein-mediated anti-adipogenic cascade. Small interfering RNA-mediated silencing of STAT3 or SMAD2/3 blunted the inhibitory effects of butein on adipogenesis indicating that an interaction between two signaling pathways is required for the action of butein. Upon butein treatments, stimulation of TGF- β signaling was still preserved in STAT3 silenced cells, whereas regulation of STAT3 signaling by butein was signifi- cantly impaired in SMAD2/3 silenced cells, further showing that TGF- β acts upstream of STAT3 in the butein-mediated anti-adipogenesis. Taken together, the present study shows that butein, a novel anti-adipogenic compound from RVS, inhibits adipocyte differentiation through the TGF- β pathway followed by STAT3 and peroxisome proliferatoractivated receptor γ signaling, further implicating potential roles of butein in TGF- β - and STAT3-dysregulated diseases.-
dc.publisherAmer Soc Biochemistry Molecular Biology Inc-
dc.titleButein is a novel anti-adipogenic compound-
dc.title.alternativeButein is a novel anti-adipogenic compound-
dc.typeArticle-
dc.citation.titleJournal of Lipid Research-
dc.citation.number5-
dc.citation.endPage1396-
dc.citation.startPage1385-
dc.citation.volume54-
dc.contributor.affiliatedAuthorJeong Soo Lee-
dc.contributor.alternativeName송노준-
dc.contributor.alternativeName윤향진-
dc.contributor.alternativeName김기현-
dc.contributor.alternativeName정소라-
dc.contributor.alternativeName장우석-
dc.contributor.alternativeName서초롱-
dc.contributor.alternativeName이영민-
dc.contributor.alternativeName권대혁-
dc.contributor.alternativeName홍정우-
dc.contributor.alternativeName이정수-
dc.contributor.alternativeName박기문-
dc.contributor.alternativeName이강로-
dc.contributor.alternativeName박계원-
dc.identifier.bibliographicCitationJournal of Lipid Research, vol. 54, no. 5, pp. 1385-1396-
dc.identifier.doi10.1194/jlr.M035576-
dc.subject.keyword3T3-L1-
dc.subject.keywordAdipocyte differentiation-
dc.subject.keywordButein-
dc.subject.keywordC3H10T1/2-
dc.subject.keywordGenistein-
dc.subject.keywordObesity-
dc.subject.keywordPeroxisome proliferator-activated receptor γ-
dc.subject.keywordResveratrol-
dc.subject.keywordRhus verniciflua Stokes-
dc.subject.local3T3-L1-
dc.subject.localadipocyte differentiation-
dc.subject.localAdipocyte differentiation-
dc.subject.localButein-
dc.subject.localC3H10T1/2-
dc.subject.localgenistein-
dc.subject.localGenistein-
dc.subject.localObesity-
dc.subject.localobesity-
dc.subject.localPeroxisome proliferator-activated receptor γ-
dc.subject.localperoxisome proliferators-activated receptor γ-
dc.subject.localResveratrol-
dc.subject.localresveratrol-
dc.subject.localRhus verniciflua Stokes-
dc.description.journalClassY-
Appears in Collections:
Division of A.I. & Biomedical Research > Microbiome Convergence Research Center > 1. Journal Articles
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