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Authordc.contributor.authorKohan Ivani, Karla 
Authordc.contributor.authorGabler Neale, Fernando 
Authordc.contributor.authorSelman, 
Authordc.contributor.authorVega Blanco, María Margarita 
Authordc.contributor.authorRomero Osses, Carmen 
Admission datedc.date.accessioned2019-03-18T11:53:43Z
Available datedc.date.available2019-03-18T11:53:43Z
Publication datedc.date.issued2016
Cita de ítemdc.identifier.citationJournal of Cancer Research and Clinical Oncology, Volumen 142, Issue 1, 2018, Pages 47-58
Identifierdc.identifier.issn14321335
Identifierdc.identifier.issn01715216
Identifierdc.identifier.other10.1007/s00432-015-1998-y
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/166712
Abstractdc.description.abstract© 2015, The Author(s).Purpose: One of the hypotheses regarding the genesis of epithelial ovarian cancer involves the action of androgens on the proliferation of epithelial ovarian cells, as well as inclusion cysts. The purpose of the present study was to evaluate whether DHT causes changes in the TGF-β1 pathway that might modify the anti-proliferative effect of the latter. Methods: The levels of TGF-β1 protein, of its receptors (TGFBR1 and TGFBR2), of Smad2/3 (canonical signaling pathway protein) and of p21 (cell cycle protein) were assessed in ovarian tissues, epithelial ovarian cancer cell lines (A2780) and control cell lines (HOSE) through the use of immunohistochemistry and immunocytochemistry. Additionally, cell lines were treated with 100 nmol/L DHT, 10 ng/mL of TGF-β1 and DHT + TGF-β1 during 72 h in the presence and absence of a siRNA against androgen receptor. After treatment, TGFBR1 and TGFBR2 levels were detected through Western blotting and p21 was assessed through immunocyt
Lenguagedc.language.isoen
Publisherdc.publisherSpringer Verlag
Type of licensedc.rightsAttribution-NonCommercial-NoDerivs 3.0 Chile
Link to Licensedc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/cl/
Sourcedc.sourceJournal of Cancer Research and Clinical Oncology
Keywordsdc.subjectAndrogen receptor
Keywordsdc.subjectEpithelial ovarian cancer
Keywordsdc.subjectTGF-β signaling pathway
Títulodc.titleRole of dihydrotestosterone (DHT) on TGF-β1 signaling pathway in epithelial ovarian cancer cells
Document typedc.typeArtículo de revista
dcterms.accessRightsdcterms.accessRightsAcceso Abierto
Catalogueruchile.catalogadorSCOPUS
Indexationuchile.indexArtículo de publicación SCOPUS
uchile.cosechauchile.cosechaSI


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Attribution-NonCommercial-NoDerivs 3.0 Chile
Except where otherwise noted, this item's license is described as Attribution-NonCommercial-NoDerivs 3.0 Chile