A polymorphism in the GALNT2 gene and ovarian cancer risk in four population based case-control studies

  • Kathryn L. Terry
  • , Allison F. Vitonis
  • , Dena Hernandez
  • , Galina Lurie
  • , Honglin Song
  • , Susan J. Ramus
  • , Linda Titus-Ernstoff
  • , Michael E. Carney
  • , Lynne R. Wilkens
  • , Aleksandra Gentry-Maharaj
  • , Usha Menon
  • , Simon A. Gayther
  • , Paul D. Pharaoh
  • , Marc T. Goodman
  • , Daniel W. Cramer
  • , Michael J. Birrer

Producción científica: Articlerevisión exhaustiva

6 Citas (Scopus)

Resumen

Recent epidemiologic evidence supports a role for MUC1 in ovarian carcinogenesis; therefore, we hypothesized that common genetic variation in the genes responsible for glycosylation of MUC1 may influence ovarian cancer risk. In a genome-wide association study of ovarian cancer, we observed an association between a non-synonymous SNP (rs2271077) in the UDP-N-acetyl-alpha-d-galactosamine: polypeptide N-acetylgalactosainyltransferase 2 (GALNT2) gene and ovarian cancer risk (p=0.005). We sought to validate the association in four population based ovarian cancer case-control studies collaborating through the Ovarian Cancer Association Consortium. Although rs2271077 was associated with a significantly increased risk (Odds Ratio (OR) = 1.37, 95% Confidence Interval (CI) =1.06-1.77) in one study with 961 cases and 922 controls, we observed no association in the remaining three studies including 1452 cases and 1954 controls (OR=0.83, 95% CI= 0.66-1.04). Therefore, there appears to be no strong evidence of association between GALNT2 SNP rs2271077 and ovarian cancer risk.

Idioma originalEnglish (US)
Páginas (desde-hasta)272-277
Número de páginas6
PublicaciónInternational Journal of Molecular Epidemiology and Genetics
Volumen1
N.º4
EstadoPublished - 2010
Publicado de forma externa

ASJC Scopus subject areas

  • Epidemiology
  • Genetics
  • Genetics(clinical)

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