학술논문

Five endometrial cancer risk loci identified through genome-wide association analysis
Document Type
Article
Author
Cheng, Timothy H TThompson, Deborah JO'Mara, Tracy APainter, Jodie NGlubb, Dylan MFlach, SusanneLewis, AnnabelleFrench, Juliet DFreeman-Mills, LukeChurch, DavidGorman, MaggieMartin, LynnHodgson, ShirleyWebb, Penelope MAttia, JohnHolliday, Elizabeth GMcEvoy, MarkScott, Rodney JHenders, Anjali KMartin, Nicholas GMontgomery, Grant WNyholt, Dale RAhmed, ShahanaHealey, Catherine SShah, MitulDennis, JoeFasching, Peter ABeckmann, Matthias WHein, AlexanderEkici, Arif BHall, PerCzene, KamilaDarabi, HatefLi, JingmeiDörk, ThiloDürst, MatthiasHillemanns, PeterRunnebaum, IngoAmant, FredericSchrauwen, StefanieZhao, HuiLambrechts, DietherDepreeuw, JeroenDowdy, Sean CGoode, Ellen LFridley, Brooke LWinham, Stacey JNjølstad, Tormund SSalvesen, Helga BTrovik, JoneWerner, Henrica M JAshton, KatieOtton, GeoffreyProietto, TonyLiu, TaoMints, MiriamTham, EmmaLi, Mulin JunYip, Shun HWang, JunwenBolla, Manjeet KMichailidou, KyriakiWang, QinTyrer, Jonathan PDunlop, MalcolmHoulston, RichardPalles, ClaireHopper, John LPeto, JulianSwerdlow, Anthony JBurwinkel, BarbaraBrenner, HermannMeindl, AlfonsBrauch, HiltrudLindblom, AnnikaChang-Claude, JennyCouch, Fergus JGiles, Graham GKristensen, Vessela NCox, AngelaCunningham, Julie MPharoah, Paul D PDunning, Alison MEdwards, Stacey LEaston, Douglas FTomlinson, IanSpurdle, Amanda B
Source
Nature Genetics; May 2016, Vol. 48 Issue: 6 p667-674, 8p
Subject
Language
ISSN
10614036; 15461718
Abstract
We conducted a meta-analysis of three endometrial cancer genome-wide association studies (GWAS) and two follow-up phases totaling 7,737 endometrial cancer cases and 37,144 controls of European ancestry. Genome-wide imputation and meta-analysis identified five new risk loci of genome-wide significance at likely regulatory regions on chromosomes 13q22.1 (rs11841589, near KLF5), 6q22.31 (rs13328298, in LOC643623 and near HEY2 and NCOA7), 8q24.21 (rs4733613, telomeric to MYC), 15q15.1 (rs937213, in EIF2AK4, near BMF) and 14q32.33 (rs2498796, in AKT1, near SIVA1). We also found a second independent 8q24.21 signal (rs17232730). Functional studies of the 13q22.1 locus showed that rs9600103 (pairwise r2= 0.98 with rs11841589) is located in a region of active chromatin that interacts with the KLF5 promoter region. The rs9600103[T] allele that is protective in endometrial cancer suppressed gene expression in vitro, suggesting that regulation of the expression of KLF5, a gene linked to uterine development, is implicated in tumorigenesis. These findings provide enhanced insight into the genetic and biological basis of endometrial cancer.