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dc.contributor.authorGiacomazzi, Julianapt_BR
dc.contributor.authorAguiar, E.pt_BR
dc.contributor.authorPalmero, Edenir Inêzpt_BR
dc.contributor.authorSchmidt, Adriana Vidalpt_BR
dc.contributor.authorSkonieski, Giovanapt_BR
dc.contributor.authorFilho, D.pt_BR
dc.contributor.authorBock, Hugopt_BR
dc.contributor.authorPereira, Maria Luiza Saraivapt_BR
dc.contributor.authorEwald, Ingrid Petronipt_BR
dc.contributor.authorFaccini, Lavinia Schulerpt_BR
dc.contributor.authorCamey, Suzi Alvespt_BR
dc.contributor.authorCaleffi, Mairapt_BR
dc.contributor.authorGiugliani, Robertopt_BR
dc.contributor.authorProlla, Patrícia Ashtonpt_BR
dc.date.accessioned2014-02-27T01:50:54Zpt_BR
dc.date.issued2012pt_BR
dc.identifier.issn0100-879Xpt_BR
dc.identifier.urihttp://hdl.handle.net/10183/87816pt_BR
dc.description.abstractPolymorphisms of hormone receptor genes have been linked to modifications in reproductive factors and to an increased risk of breast cancer (BC). In the present study, we have determined the allelic and genotypic frequencies of the ERα-397 PvuII C/T, ERα-351 XbaI A/G and PGR PROGINS polymorphisms and investigated their relationship with mammographic density, body mass index (BMI) and other risk factors for BC. A consecutive and unselected sample of 750 Brazilian BC-unaffected women enrolled in a mammography screening program was recruited. The distribution of PGR PROGINS genotypic frequencies was 72.5, 25.5 and 2.0% for A1A1, A1A2 and A2A2, respectively, which was equivalent to that encountered in other studies with healthy women. The distribution of ERα genotypes was: ERα-397 PvuII C/T: 32.3% TT, 47.5% TC, and 20.2% CC; ERα-351 XbaI A/G: 46.3% AA, 41.7% AG and 12.0% GG. ERα haplotypes were 53.5% PX, 14.3% Px, 0.3% pX, and 32.0% px. These were significantly different from most previously published reports worldwide (P < 0.05). Overall, the PGR PROGINS genotypes A2A2 and A1A2 were associated with fatty and moderately fatty breast tissue. The same genotypes were also associated with a high BMI in postmenopausal women. In addition, the ERα-351 XbaI GG genotype was associated with menarche ≥12 years (P = 0.02). ERα and PGR polymorphisms have a phenotypic effect and may play an important role in BC risk determination. Finally, if confirmed in BC patients, these associations could have important implications for mammographic screening and strategies and may be helpful to identify women at higher risk for the disease.en
dc.format.mimetypeapplication/pdfpt_BR
dc.language.isoengpt_BR
dc.relation.ispartofBrazilian journal of medical and biological research = Revista brasileira de pesquisas médicas e biológicas. Ribeirao Preto. Vol. 45, n. 10 (oct. 2012), p. 891-897pt_BR
dc.rightsOpen Accessen
dc.subjectPolimorfismo genéticopt_BR
dc.subjectGenetic polymorphismsen
dc.subjectEstrogen receptor geneen
dc.subjectReceptores estrogenicospt_BR
dc.subjectReceptores de progesteronapt_BR
dc.subjectProgesterone receptor geneen
dc.subjectNeoplasias da mamapt_BR
dc.subjectBreast cancer susceptibilityen
dc.titlePrevalence of ERα-397 PvuII C/T, ERα-351 XbaI A/G and PGR PROGINS polymorphisms in Brazilian breast cancer-unaffected womenpt_BR
dc.typeArtigo de periódicopt_BR
dc.identifier.nrb000866207pt_BR
dc.type.originNacionalpt_BR


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