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The effects of genistein and daidzein on cell proliferation kinetics in HT29 colon cancer cells: the expression of CTNNBIP1 (beta-catenin), APC (adenomatous polyposis coli) and BIRC5 (survivin)

dc.contributor.authorLepri, Sandra Regina
dc.contributor.authorZanelatto, Leonardo Campos
dc.contributor.authorGoncalves da Silva, Patricia Benites
dc.contributor.authorSartori, Daniele
dc.contributor.authorRibeiro, Lucia Regina [UNESP]
dc.contributor.authorMantovani, Mario Sergio
dc.contributor.institutionUniversidade Estadual de Londrina (UEL)
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2014-12-03T13:09:01Z
dc.date.available2014-12-03T13:09:01Z
dc.date.issued2014-04-01
dc.description.abstractSoybean isoflavonoids have received significant attention due to their potential anticarcinogenic and antiproliferative effects and possible role in many signal transduction pathways. However, their mechanisms of action and their molecular targets remain to be further elucidated. In this paper, we demonstrated that two soybean isoflavones (genistein and daidzein) reduced the proliferation of the human colon adenocarcinoma grade II cell line (HT-29) at concentrations of 25 and 50-100 mu M, respectively. We then investigated the effects of genistein and daidzein by RT-PCR on molecules that involved in tumor development and progression by their regulation of cell proliferation. At a concentration of 50 mu M genistein, there was suppressed expression of beta-catenin (CTNNBIP1). Neither genistein nor daidzein affected APC (adenomatous polyposis coli) or survivin (BIRC5) expression when cells were treated with concentrations of 10 or 50 mu M. These data suggest that the down-regulation of beta-catenin by genistein may constitute an important determinant of the suppression of HT-29 cell growth and may be exploited for the prevention and treatment of colon cancer.en
dc.description.affiliationState Univ Londrina UEL, Dept Gen Biol, BR-86051980 Londrina, PR, Brazil
dc.description.affiliationSao Paulo State Univ, UNESP, Inst Biosci, BR-18618970 Botucatu, SP, Brazil
dc.description.affiliationUnespSao Paulo State Univ, UNESP, Inst Biosci, BR-18618970 Botucatu, SP, Brazil
dc.format.extent78-84
dc.identifierhttp://dx.doi.org/10.1007/s13577-012-0051-6
dc.identifier.citationHuman Cell. Tokyo: Springer Japan Kk, v. 27, n. 2, p. 78-84, 2014.
dc.identifier.doi10.1007/s13577-012-0051-6
dc.identifier.issn1749-0774
dc.identifier.urihttp://hdl.handle.net/11449/111835
dc.identifier.wosWOS:000333350000005
dc.language.isoeng
dc.publisherSpringer
dc.relation.ispartofHuman Cell
dc.relation.ispartofjcr2.109
dc.rights.accessRightsAcesso restritopt
dc.sourceWeb of Science
dc.subjectGenisteinen
dc.subjectDaidzeinen
dc.subjectProliferation kineticsen
dc.subjectbeta-cateninen
dc.subjectSurvivingen
dc.subjectAPCen
dc.subjectHT29 cellen
dc.titleThe effects of genistein and daidzein on cell proliferation kinetics in HT29 colon cancer cells: the expression of CTNNBIP1 (beta-catenin), APC (adenomatous polyposis coli) and BIRC5 (survivin)en
dc.typeArtigopt
dcterms.licensehttp://www.springer.com/open+access/authors+rights?SGWID=0-176704-12-683201-0
dcterms.rightsHolderSpringer
dspace.entity.typePublication
unesp.author.orcid0000-0001-5268-6508[6]
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Biociências, Botucatupt

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