Details

Autor(en) / Beteiligte

• Permuth-Wey, Jennifer
• Shen, Howard C
• Tyrer, Jonathan P
• Chen, Zhihua
• Lin, Hui-Yi
• Chen, Y Ann
• Ramus, Susan J
• Karevan, Rod
• Larson, Melissa C
• Anton-Culver, Hoda
• Armasu, Sebastian M
• Bacot, François
• Bandera, Elisa V
• Barnholtz-Sloan, Jill
• Bloom, Greg
• Brooks-Wilson, Angela
• Brown, Robert
• Butzow, Ralf
• Cai, Qiuyin
• Campbell, Ian
• Chenevix-Trench, Georgia
• Coetzee, Gerhard A
• Cook, Linda S
• Couch, Fergus J
• Cramer, Daniel W
• Cunningham, Julie M
• Despierre, Evelyn
• Doherty, Jennifer A
• du Bois, Andreas
• Dürst, Matthias
• Easton, Douglas F
• Edwards, Robert
• Ekici, Arif B
• Fenstermacher, David A
• Flanagan, James M
• Garcia-Closas, Montserrat
• Goodman, Marc T
• Gore, Martin
• Gronwald, Jacek
• Halle, Mari K
• Harter, Philipp
• Hillemanns, Peter
• Høgdall, Claus K
• Hosono, Satoyo
• Jakubowska, Anna
• Jensen, Allan
• Jim, Heather
• Kalli, Kimberly R
• Kaye, Stanley B
• Kelemen, Linda E
• Kikkawa, Fumitaka
• Konecny, Gottfried E
• Krakstad, Camilla
• Kjaer, Susanne Krüger
• Kupryjanczyk, Jolanta
• Lancaster, Johnathan M
• Le, Nhu D
• Liang, Dong
• Lim, Boon Kiong
• Lin, Jie
• Lissowska, Jolanta
• Lu, Karen H
• Matsuo, Keitaro
• Moysich, Kirsten B
• Ness, Roberta B
• Nevanlinna, Heli
• Odunsi, Kunle
• Orlow, Irene
• Pejovic, Tanja
• Pike, Malcolm C
• Poole, Elizabeth M
• Renner, Stefan P
• Rodriguez-Rodriguez, Lorna
• Rossing, Mary Anne
• Rzepecka, Iwona K
• Salvesen, Helga B
• Severi, Gianluca
• Shu, Xiao-Ou
• Shvetsov, Yurii B
• Song, Honglin
• Spiewankiewicz, Beata
• Stram, Daniel
• Sutphen, Rebecca
• Teo, Soo-Hwang
• Terry, Kathryn L
• Thompson, Pamela J
• van Altena, Anne M
• Vergote, Ignace
• Vierkant, Robert A
• Wang-Gohrke, Shan
• Palmieri Weber, Rachel
• Wik, Elisabeth
• Wilkens, Lynne R
• Woo, Yin Ling
• Ziogas, Argyrios
• Phelan, Catherine M
• Berchuck, Andrew
• Fridley, Brooke L
• Pharoah, Paul D P
• Sellers, Thomas A

Titel

Identification and molecular characterization of a new ovarian cancer susceptibility locus at 17q21.31

Ist Teil von

• Nature communications, 2013, Vol.4 (1), p.1627-1627, Article 1627

Ort / Verlag

England: Nature Publishing Group

Erscheinungsjahr

2013

Quelle

Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals

Beschreibungen/Notizen

• Epithelial ovarian cancer (EOC) has a heritable component that remains to be fully characterized. Most identified common susceptibility variants lie in non-protein-coding sequences. We hypothesized that variants in the 3' untranslated region at putative microRNA (miRNA)-binding sites represent functional targets that influence EOC susceptibility. Here, we evaluate the association between 767 miRNA-related single-nucleotide polymorphisms (miRSNPs) and EOC risk in 18,174 EOC cases and 26,134 controls from 43 studies genotyped through the Collaborative Oncological Gene-environment Study. We identify several miRSNPs associated with invasive serous EOC risk (odds ratio=1.12, P=10(-8)) mapping to an inversion polymorphism at 17q21.31. Additional genotyping of non-miRSNPs at 17q21.31 reveals stronger signals outside the inversion (P=10(-10)). Variation at 17q21.31 is associated with neurological diseases, and our collaboration is the first to report an association with EOC susceptibility. An integrated molecular analysis in this region provides evidence for ARHGAP27 and PLEKHM1 as candidate EOC susceptibility genes.