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Title: Genome-wide association study identifies a common variant associated with risk of endometrial cancer.
Authors: Spurdle AB,  Thompson DJ,  Ahmed S,  Ferguson K,  Healey CS,  O'Mara T,  Walker LC,  Montgomery SB,  Dermitzakis ET,  Australian National Endometrial Cancer Study Group,  Fahey P,  Montgomery GW,  Webb PM,  Fasching PA,  Beckmann MW,  Ekici AB,  Hein A,  Lambrechts D,  Coenegrachts L,  Vergote I,  Amant F,  Salvesen HB,  Trovik J,  Njolstad TS,  Helland H,  Scott RJ,  Ashton K,  Proietto T,  Otton G,  National Study of Endometrial Cancer Genetics Group,  Tomlinson I,  Gorman M,  Howarth K,  Hodgson S,  Garcia-Closas M,  Wentzensen N,  Yang H,  Chanock S,  Hall P,  Czene K,  Liu J,  Li J,  Shu XO,  Zheng W,  Long J,  Xiang YB,  Shah M,  Morrison J,  Michailidou K,  Pharoah PD,  Dunning AM,  Easton DF
Journal: Nat Genet
Date: 2011 May
Branches: CGR, HREB, LTG
PubMed ID: 21499250
PMC ID: PMC3770523
Abstract: Endometrial cancer is the most common malignancy of the female genital tract in developed countries. To identify genetic variants associated with endometrial cancer risk, we performed a genome-wide association study involving 1,265 individuals with endometrial cancer (cases) from Australia and the UK and 5,190 controls from the Wellcome Trust Case Control Consortium. We compared genotype frequencies in cases and controls for 519,655 SNPs. Forty seven SNPs that showed evidence of association with endometrial cancer in stage 1 were genotyped in 3,957 additional cases and 6,886 controls. We identified an endometrial cancer susceptibility locus close to HNF1B at 17q12 (rs4430796, P = 7.1 × 10(-10)) that is also associated with risk of prostate cancer and is inversely associated with risk of type 2 diabetes.