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| Content Provider | PubMed Central |
|---|---|
| Author | Jennifer, Permuth-wey Lawrenson, Kate Shen, Howard C. Velkova, Aneliya Tyrer, Jonathan P. Chen, Zhihua Lin, Hui-yi Chen, Y. Ann Tsai, Ya-yu Qu, Xiaotao Ramus, Susan J. Rod, Karevan Lee, Janet Lee, Nathan Larson, Melissa C. Aben, Katja K. Hoda, Anton-culver Natalia, Antonenkova Antoniou, Antonis Armasu, Sebastian M. Bacot, François Baglietto, Laura Bandera, Elisa V. Jill, Barnholtz-sloan Beckmann, Matthias W. Birrer, Michael J. Bloom, Greg Bogdanova, Natalia Brinton, Louise A. Angela, Brooks-wilson Brown, Robert Ralf, Butzow Cai, Qiuyin Campbell, Ian Jenny, Chang-claude Chanock, Stephen Chenevix Trench, Georgia Cheng, Jin Q. Cicek, Mine S. Coetzee, Gerhard A. Cook, Linda S. Couch, Fergus J. Cramer, Daniel W. Cunningham, Julie M. Dansonka-mieszkowska, Agnieszka Evelyn, Despierre Doherty, Jennifer A. Thilo, Dörk Bois, Andreas Du Dürst, Matthias Easton, Douglas F. Eccles, Diana Edwards, Robert Ekici, Arif B. Fasching, Peter A. Fenstermacher, David A. Flanagan, James M. Montserrat, Garcia-closas Gentry-maharaj, Aleksandra Giles, Graham G. Glasspool, Rosalind M. Jesus, Gonzalez-bosquet Goodman, Marc T. Gore, Martin Górski, Bohdan Gronwald, Jacek Hall, Per Halle, Mari K. Harter, Philipp Heitz, Florian Hillemanns, Peter Maureen, Hoatlin Høgdall, Claus K. Høgdall, Estrid Hosono, Satoyo Jakubowska, Anna Jensen, Allan Jim, Heather Kalli, Kimberly R. Karlan, Beth Y. Kaye, Stanley B. Kelemen, Linda E. Kiemeney, Lambertus A. Kikkawa, Fumitaka Konecny, Gottfried E. Krakstad, Camilla Kjaer, Susanne Krüger Kupryjanczyk, Jolanta Lambrechts, Diether Lambrechts, Sandrina Lancaster, Johnathan M. Le, Nhu D. Leminen, Arto Levine, Douglas A. Liang, Dong Lim, Boon Kiong Lin, Jie Lissowska, Jolanta Lu, Karen H. Jan, Lubiński Lurie, Galina Massuger, Leon F. A. G. Matsuo, Keitaro Mcguire, Valerie Mclaughlin, John R. Menon, Usha Modugno, Francesmary Moysich, Kirsten B. Nakanishi, Toru Steven A., Narod Nedergaard, Lotte Ness, Roberta B. Nevanlinna, Heli Nickels, Stefan Noushmehr, Houtan Odunsi, Kunle Olson, Sara H. Orlow, Irene Paul, James Pearce, Celeste L. Pejovic, Tanja Pelttari, Liisa M. Pike, Malcolm C. Poole, Elizabeth M. Raska, Paola Renner, Stefan P. Risch, Harvey A. Rodriguez Rodriguez, Lorna Rossing, Mary Anne Rudolph, Anja Runnebaum, Ingo B. Rzepecka, Iwona K. Salvesen, Helga B. Schwaab, Ira Severi, Gianluca Shridhar, Vijayalakshmi Shu, Xiao-ou Shvetsov, Yurii B. Sieh, Weiva Song, Honglin Southey, Melissa C. Beata, Spiewankiewicz Stram, Daniel Sutphen, Rebecca Teo, Soo-hwang Terry, Kathryn L. Tessier, Daniel C. Thompson, Pamela J. Tworoger, Shelley S. Altena, Anne M. Van Vergote, Ignace Vierkant, Robert A. Vincent, Daniel Vitonis, Allison F. Shan, Wang-gohrke Weber, Rachel Palmieri Nicolas, Wentzensen Whittemore, Alice S. Wik, Elisabeth Wilkens, Lynne R. Winterhoff, Boris Woo, Yin Ling Wu, Anna H. Xiang, Yong-bing Yang, Hannah P. Zheng, Wei Ziogas, Argyrios Zulkifli, Famida Phelan, Catherine M. Iversen, Edwin Schildkraut, Joellen M. Andrew, Berchuck Fridley, Brooke L. Goode, Ellen L. Pharoah, Paul D. P. Monteiro, Alvaro N. A. Sellers, Thomas A. Gayther, Simon A. |
| Abstract | 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 binding site 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 (OR=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 associates 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. |
| Related Links | http://dx.doi.org/10.1038/ncomms2613 |
| Ending Page | 1627 |
| Page Count | 1 |
| Starting Page | 1627 |
| File Format | |
| ISSN | 20411723 |
| e-ISSN | 20411723 |
| Journal | Nature communications |
| Volume Number | 4 |
| Language | English |
| Publisher Date | 2013-01-01 |
| Access Restriction | Open |
| Subject Keyword | Research in Higher Education |
| Content Type | Text |
| Resource Type | Article |
| Subject | Chemistry Physics and Astronomy Biochemistry, Genetics and Molecular Biology |
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