Common variants at 19p13 are associated with susceptibility to ovarian cancer

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

  • Kelly L Bolton
  • Jonathan Tyrer
  • Honglin Song
  • Susan J Ramus
  • Maria Notaridou
  • Chris Jones
  • Tanya Sher
  • Aleksandra Gentry-Maharaj
  • Eva Wozniak
  • Ya-Yu Tsai
  • Joanne Weidhaas
  • Daniel Paik
  • David J Van Den Berg
  • Daniel O Stram
  • Celeste Leigh Pearce
  • Anna H Wu
  • Wendy Brewster
  • Hoda Anton-Culver
  • Argyrios Ziogas
  • Steven A Narod
  • Douglas A Levine
  • Stanley B Kaye
  • Robert Brown
  • Jim Paul
  • James Flanagan
  • Weiva Sieh
  • Valerie McGuire
  • Alice S Whittemore
  • Ian Campbell
  • Martin E Gore
  • Jolanta Lissowska
  • Hanna P Yang
  • Krzysztof Medrek
  • Jacek Gronwald
  • Jan Lubinski
  • Anna Jakubowska
  • Nhu D Le
  • Linda S Cook
  • Linda E Kelemen
  • Angela Brook-Wilson
  • Leon F A G Massuger
  • Lambertus A Kiemeney
  • Katja K H Aben
  • Anne M van Altena
  • Richard Houlston
  • Ian Tomlinson
  • Rachel T Palmieri
  • Patricia G Moorman
  • Høgdall, Estrid Vilma Solyom
  • Høgdall, Claus Kim
  • Australian Ovarian Cancer Study Group
Epithelial ovarian cancer (EOC) is the leading cause of death from gynecological malignancy in the developed world, accounting for 4% of the deaths from cancer in women. We performed a three-phase genome-wide association study of EOC survival in 8,951 individuals with EOC (cases) with available survival time data and a parallel association analysis of EOC susceptibility. Two SNPs at 19p13.11, rs8170 and rs2363956, showed evidence of association with survival (overall P = 5 × 10¿4 and P = 6 × 10¿4, respectively), but they did not replicate in phase 3. However, the same two SNPs demonstrated genome-wide significance for risk of serous EOC (P = 3 × 10¿¿ and P = 4 × 10¿¹¹, respectively). Expression analysis of candidate genes at this locus in ovarian tumors supported a role for the BRCA1-interacting gene C19orf62, also known as MERIT40, which contains rs8170, in EOC development.
OriginalsprogEngelsk
TidsskriftNature Genetics
Vol/bind42
Udgave nummer10
Sider (fra-til)880-4
Antal sider5
ISSN1061-4036
DOI
StatusUdgivet - 1 okt. 2010

ID: 34122243