A genome-wide association study yields five novel thyroid cancer risk loci

نویسندگان

  • Julius Gudmundsson
  • Gudmar Thorleifsson
  • Jon K Sigurdsson
  • Lilja Stefansdottir
  • Jon G Jonasson
  • Sigurjon A Gudjonsson
  • Daniel F Gudbjartsson
  • Gisli Masson
  • Hrefna Johannsdottir
  • Gisli H Halldorsson
  • Simon N Stacey
  • Hannes Helgason
  • Patrick Sulem
  • Leigha Senter
  • Huiling He
  • Sandya Liyanarachchi
  • Matthew D Ringel
  • Esperanza Aguillo
  • Angeles Panadero
  • Enrique Prats
  • Almudena Garcia-Castaño
  • Ana De Juan
  • Fernando Rivera
  • Li Xu
  • Lambertus A Kiemeney
  • Gudmundur I Eyjolfsson
  • Olof Sigurdardottir
  • Isleifur Olafsson
  • Hoskuldur Kristvinsson
  • Romana T Netea-Maier
  • Thorvaldur Jonsson
  • Jose I Mayordomo
  • Theo S Plantinga
  • Hannes Hjartarson
  • Jon Hrafnkelsson
  • Erich M Sturgis
  • Unnur Thorsteinsdottir
  • Thorunn Rafnar
  • Albert de la Chapelle
  • Kari Stefansson
چکیده

The great majority of thyroid cancers are of the non-medullary type. Here we report findings from a genome-wide association study of non-medullary thyroid cancer, including in total 3,001 patients and 287,550 controls from five study groups of European descent. Our results yield five novel loci (all with Pcombined<3 × 10-8): 1q42.2 (rs12129938 in PCNXL2), 3q26.2 (rs6793295 a missense mutation in LRCC34 near TERC), 5q22.1 (rs73227498 between NREP and EPB41L4A), 10q24.33 (rs7902587 near OBFC1), and two independently associated variants at 15q22.33 (rs2289261 and rs56062135; both in SMAD3). We also confirm recently published association results from a Chinese study of a variant on 5p15.33 (rs2736100 near the TERT gene) and present a stronger association result for a moderately correlated variant (rs10069690; OR=1.20, P=3.2 × 10-7) based on our study of individuals of European ancestry. In combination, these results raise several opportunities for future studies of the pathogenesis of thyroid cancer.

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عنوان ژورنال:

دوره 8  شماره 

صفحات  -

تاریخ انتشار 2017