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dc.contributor.author Mervai Z,
dc.contributor.author Sólyomváry, Anna
dc.contributor.author Tóth, Gergő
dc.contributor.author Noszál, Béla
dc.contributor.author Perlné Molnár, Ibolya
dc.contributor.author Baghy, Kornélia
dc.contributor.author Kovalszky, Ilona
dc.date.accessioned 2015-03-28T18:19:03Z
dc.date.available 2015-03-28T18:19:03Z
dc.date.issued 2015
dc.identifier 84911926463
dc.identifier.citation pagination=19-26; journalVolume=100; journalTitle=FITOTERAPIA;
dc.identifier.uri http://repo.lib.semmelweis.hu//handle/123456789/1644
dc.identifier.uri doi:10.1016/j.fitote.2014.10.017
dc.description.abstract The molecular constituents of Cirsium brachycephalum fruits were identified, quantified and isolated for the first time. The lignan glycoside tracheloside was the main compound, which was transformed quantitatively into its aglycone trachelogenin by endogenous enzymatic treatment of the fruit. Following this transformation by high performance liquid chromatography (HPLC) hyphenated with UV and mass spectrometry (MS) detections on a quantitative basis, the enzyme-hydrolyzed fruit was found to be the richest raw material containing trachelogenin (17.2mg/g) reported to date. Thus, the enzyme-hydrolyzed fruit was used to isolate trachelogenin using preparative HPLC in order to (1) unambiguously confirm its identity by gas chromatography-MS, nuclear magnetic resonance spectroscopy and optical rotation, and (2) investigate its in vitro antiproliferative activities against the SW480 colon adenocarcinoma cell line. Trachelogenin significantly affected the phosphorylation of key proteins such as beta-Catenin, c-Myc and GSK3 in the beta-Catenin signaling pathway in a concentration-dependent manner. These changes account for the antiproliferative effects of trachelogenin.
dc.relation.ispartof urn:issn:0367-326X
dc.title Endogenous enzyme-hydrolyzed fruit of Cirsium brachycephalum: Optimal source of the antiproliferative lignan trachelogenin regulating the Wnt/beta-Catenin signaling pathway in the SW480 colon adenocarcinoma cell line.
dc.type Journal Article
dc.date.updated 2015-03-28T18:18:31Z
dc.language.rfc3066 en
dc.identifier.mtmt 2788762
dc.identifier.pubmed 25447161
dc.contributor.department SE/GYTK/Gyógyszerészi Kémiai Intézet
dc.contributor.department SE/AOK/I/I. Sz. Patológiai és Kísérleti Rákkutató Intézet
dc.contributor.institution Semmelweis Egyetem


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