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


Ontology type: schema:ScholarlyArticle      Open Access: True


Article Info

DATE

2013-12

AUTHORS

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 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, Vijayalakshmi 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

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. More... »

PAGES

1627

Journal

TITLE

Nature Communications

ISSUE

1

VOLUME

4

Author Affiliations

  • Moffitt Cancer Center
  • University of Southern California
  • University of Cambridge
  • Mayo Clinic
  • Radboud University Nijmegen Medical Centre
  • University of California, Irvine
  • QIMR Berghofer Medical Research Institute
  • Peter MacCallum Cancer Centre
  • University of Melbourne
  • Rutgers University
  • Case Western Reserve University
  • Massachusetts General Hospital
  • Hannover Medical School
  • National Cancer Institute
  • BC Cancer Agency
  • Imperial College London
  • Helsinki University Central Hospital
  • Vanderbilt University
  • German Cancer Research Center
  • University of New Mexico
  • Harvard University
  • Centrum Onkologii Instytut
  • Universitaire Ziekenhuizen Leuven
  • Dartmouth College
  • Kliniken Essen-Mitte
  • Jena University Hospital
  • University of Erlangen-Nuremberg
  • University of California Los Angeles
  • Breast Cancer Now
  • University College London
  • Monash University
  • Beatson West of Scotland Cancer Centre
  • Cedars-Sinai Medical Center
  • Royal Marsden Hospital
  • Pomeranian Medical University
  • University of Bergen
  • Oregon Health & Science University
  • Rigshospitalet
  • Danish Cancer Society
  • Aichi Cancer Center
  • Institute of Cancer Research
  • Nagoya University
  • KU Leuven
  • Memorial Sloan Kettering Cancer Center
  • Texas Southern University
  • The University of Texas MD Anderson Cancer Center
  • University of Hawaii at Manoa
  • Stanford University
  • Lunenfeld-Tanenbaum Research Institute
  • University of Pittsburgh Cancer Institute
  • Roswell Park Cancer Institute
  • Okazaki City Hospital
  • University of Toronto
  • The University of Texas Health Science Center at Houston
  • Yale University
  • University of Washington
  • University of South Florida
  • University of Ulm
  • Duke University Hospital
  • Shanghai Cancer Institute
  • Duke University
  • University of Kansas Medical Center
  • From Grant

  • Identifiers

    URI

    http://scigraph.springernature.com/pub.10.1038/ncomms2613

    DOI

    http://dx.doi.org/10.1038/ncomms2613

    DIMENSIONS

    https://app.dimensions.ai/details/publication/pub.1042390255

    PUBMED

    https://www.ncbi.nlm.nih.gov/pubmed/23535648


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