Egyszerű nézet

dc.contributor.author Dudás József
dc.contributor.author Fullár Alexandra
dc.contributor.author Angela Romani
dc.contributor.author Christian Pritz
dc.contributor.author Kovalszky Ilona
dc.contributor.author Volker Hans Schartinger
dc.contributor.author Georg Mathias Sprinzl
dc.contributor.author Herbert Riechelmann
dc.date.accessioned 2016-01-06T11:42:04Z
dc.date.available 2016-01-06T11:42:04Z
dc.date.issued 2013
dc.identifier.citation pagination=800-809;journalVolume=319;journalIssueNumber=6;journalTitle=EXPERIMENTAL CELL RESEARCH; hu
dc.identifier.uri http://repo.lib.semmelweis.hu//handle/123456789/1669
dc.identifier.uri doi:10.1016/j.yexcr.2012.12.001
dc.description.abstract Co-culture of periodontal ligament fibroblasts (PDLs) and SCC-25 oral squamous carcinoma cells (OSCC) results in conversion of PDLs into carcinoma-associated fibroblasts (CAFs) and induces epithelial-to mesenchymal transition (EMT) of OSCC tumor cells. We hypothesized that Curcumin targets this dynamic mutual interaction between CAFs and tumor cells. Normal and 2muM Curcumin-treated co-culture were performed for 4 days, followed by analysis of tumor cell invasivity, mRNA/protein expression of EMT-markers and mediators, activity measure of matrix metalloproteinase 9 (MMP-9), and western blot analysis of signal transduction in tumor cells and fibroblasts. In Curcumin-treated co-culture, in tumor cells, the levels of nuclear factor kappaB (NFkappaBalpha) and early response kinase (ERK)-decreased, in fibroblasts, integrin alphav protein synthesis decreased compared to corresponding cells in normal co-culture. The signal modulatory changes induced by Curcumin caused decreased release of EMT-mediators in CAFs and reversal of EMT in tumor cells, which was associated with decreased invasion. These data confirm the palliative potential of Curcumin in clinical application. hu
dc.relation.ispartof urn:issn:0014-4827
dc.title Curcumin targets fibroblast-tumor cell interactions in oral squamous cell carcinoma. hu
dc.type Journal Article hu
dc.date.updated 2015-04-08T12:44:51Z
dc.language.rfc3066 en hu
dc.identifier.mtmt 2233921
dc.identifier.wos 000316374600004
dc.identifier.pubmed 23247073
dc.contributor.department SE/AOK/I/I. Sz. Patológiai és Kísérleti Rákkutató Intézet
dc.contributor.institution Semmelweis Egyetem


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