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

  • Jennifer Permuth-Wey
  • , Kate Lawrenson
  • , Howard C. Shen
  • , Aneliya Velkova
  • , Jonathan P. Tyrer
  • , Zhihua Chen
  • , Hui Yi Lin
  • , Y. Ann Chen
  • , Ya Yu Tsai
  • , Xiaotao Qu
  • , Susan J. Ramus
  • , Rod Karevan
  • , Janet Lee
  • , Nathan Lee
  • , Melissa C. Larson
  • , Katja K. Aben
  • , Hoda Anton-Culver
  • , Natalia Antonenkova
  • , Antonis C. Antoniou
  • , Sebastian M. Armasu
  • François Bacot, Laura Baglietto, Elisa V. Bandera, Jill Barnholtz-Sloan, Matthias W. Beckmann, Michael J. Birrer, Greg Bloom, Natalia Bogdanova, Louise A. Brinton, Angela Brooks-Wilson, Robert Brown, Ralf Butzow, Qiuyin Cai, Ian Campbell, Jenny Chang-Claude, Stephen Chanock, Georgia Chenevix-Trench, Jin Q. Cheng, Mine S. Cicek, Gerhard A. Coetzee, Linda S. Cook, Fergus J. Couch, Daniel W. Cramer, Julie M. Cunningham, Agnieszka Dansonka-Mieszkowska, Evelyn Despierre, Jennifer A. Doherty, Thilo Dörk, Andreas Du Bois, Matthias Dürst, Douglas F. Easton, Diana Eccles, Robert Edwards, Arif B. Ekici, Peter A. Fasching, David A. Fenstermacher, James M. Flanagan, Montserrat Garcia-Closas, Aleksandra Gentry-Maharaj, Graham G. Giles, Rosalind M. Glasspool, Jesus Gonzalez-Bosquet, Marc T. Goodman, Martin Gore, Bohdan Górski, Jacek Gronwald, Per Hall, Mari K. Halle, Philipp Harter, Florian Heitz, Peter Hillemanns, Maureen Hoatlin, Claus K. Høgdall, Estrid Høgdall, Satoyo Hosono, Anna Jakubowska, Allan Jensen, Heather Jim, Kimberly R. Kalli, Beth Y. Karlan, Stanley B. Kaye, Linda E. Kelemen, Lambertus A. Kiemeney, Fumitaka Kikkawa, Gottfried E. Konecny, Camilla Krakstad, Susanne Krüger Kjaer, Jolanta Kupryjanczyk, Diether Lambrechts, Sandrina Lambrechts, Johnathan M. Lancaster, Nhu D. Le, Arto Leminen, Douglas A. Levine, Dong Liang, Boon Kiong Lim, Jie Lin, Jolanta Lissowska, Karen H. Lu, Jan Lubiński, Galina Lurie, Leon F.A.G. Massuger, Keitaro Matsuo, Valerie McGuire, John R. McLaughlin, Usha Menon, Francesmary Modugno, Kirsten B. Moysich, Toru Nakanishi, Steven A. Narod, Lotte Nedergaard, Roberta B. Ness, Heli Nevanlinna, Stefan Nickels, Houtan Noushmehr, Kunle Odunsi, Sara H. Olson, Irene Orlow, James Paul, Celeste L. Pearce, Tanja Pejovic, Liisa M. Pelttari, Malcolm C. Pike, Elizabeth M. Poole, Paola Raska, Stefan P. Renner, Harvey A. Risch, Lorna Rodriguez-Rodriguez, Mary Anne Rossing, Anja Rudolph, Ingo B. Runnebaum, Iwona K. Rzepecka, Helga B. Salvesen, Ira Schwaab, Gianluca Severi, Viji Shridhar, Xiao Ou Shu, Yurii B. Shvetsov, Weiva Sieh, Honglin Song, Melissa C. Southey, Beata Spiewankiewicz, Daniel Stram, Rebecca Sutphen, Soo Hwang Teo, Kathryn L. Terry, Daniel C. Tessier, Pamela J. Thompson, Shelley S. Tworoger, Anne M. Van Altena, Ignace Vergote, Robert A. Vierkant, Daniel Vincent, Allison F. Vitonis, Shan Wang-Gohrke, Rachel Palmieri Weber, Nicolas Wentzensen, Alice S. Whittemore, Elisabeth Wik, Lynne R. Wilkens, Boris Winterhoff, Yin Ling Woo, Anna H. Wu, Yong Bing Xiang, Hannah P. Yang, Wei Zheng, Argyrios Ziogas, Famida Zulkifli, Catherine M. Phelan, Edwin Iversen, Joellen M. Schildkraut, Andrew Berchuck, Brooke L. Fridley, Ellen L. Goode, Paul D.P. Pharoah, Alvaro N.A. Monteiro, Thomas A. Sellers, Simon A. Gayther
  • Moffitt Cancer Center
  • University of Southern California
  • University of Cambridge
  • Mayo Clinic Rochester, MN
  • Radboud University Nijmegen
  • Comprehensive Cancer Center Netherlands
  • University of California at Irvine
  • Byelorussian Institute for Oncology and Medical Radiology Aleksandrov N.N.
  • McGill University
  • Cancer Council Victoria
  • University of Melbourne
  • The State University of New Jersey
  • Case Western Reserve University
  • Friedrich-Alexander University Erlangen-Nürnberg
  • Massachusetts General Hospital
  • Hannover Medical School
  • National Institutes of Health
  • Provincial Health Services Authority
  • Imperial College London
  • University of Helsinki
  • Helsinki University Hospital
  • Vanderbilt University
  • Peter Maccallum Cancer Centre
  • German Cancer Research Center
  • Queensland Institute of Medical Research
  • University of New Mexico
  • Harvard University
  • Maria Sklodowska-Curie Institute of Oncology
  • KU Leuven
  • Dartmouth College
  • Dr. Horst Schmidt Klinik GmbH
  • Kliniken Essen-Mitte
  • Friedrich Schiller University Jena
  • University of Southampton
  • University of Pittsburgh
  • University of California at Los Angeles
  • The Institute of Cancer Research
  • University College London
  • Monash University
  • Beatson Oncology Centre
  • Cedars-Sinai Medical Center
  • Royal Marsden NHS Foundation Trust
  • Pomeranian Medical University in Szczecin
  • Karolinska Institutet
  • University of Bergen
  • Oregon Health and Science University
  • University of Copenhagen
  • Danish Cancer Society
  • Aichi Cancer Center Hospital and Research Institute
  • Alberta Health Services
  • University of Calgary
  • Nagoya University
  • Flanders Institute for Biotechnology
  • Memorial Sloan-Kettering Cancer Center
  • Texas Southern University
  • University of Malaya
  • University of Texas MD Anderson Cancer Center
  • University of Hawai'i at Mānoa
  • Stanford University
  • University of Toronto
  • Roswell Park Cancer Institute
  • University of Texas Health Science Center at Houston
  • Universidade de São Paulo
  • Brigham and Women’s Hospital
  • Yale University
  • Fred Hutchinson Cancer Research Center
  • University of Washington
  • Institut für Humangenetik Wiesbaden
  • University of South Florida
  • Sime Darby Medical Centre
  • Ulm University
  • Duke University
  • Shanghai Cancer Institute
  • University of Kansas

Research output: Contribution to journalArticlepeer-review

101 Scopus citations

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-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.

Original languageEnglish
Article number1627
JournalNature Communications
Volume4
DOIs
StatePublished - 2013

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