Literature DB >> 33527407

Multiethnic genome-wide association study of differentiated thyroid cancer in the EPITHYR consortium.

Thérèse Truong1, Fabienne Lesueur2, Pierre-Emmanuel Sugier1, Julie Guibon1,2, Constance Xhaard3,4, Mojgan Karimi1, Om Kulkarni2, Elise A Lucotte1, Delphine Bacq-Daian5, Anne Boland-Auge5, Claire Mulot6, Pierre Laurent-Puig6, Claire Schvartz7, Anne-Valérie Guizard8,9, Yan Ren3, Elisabeth Adjadj3, Frédérique Rachédi10, Francoise Borson-Chazot11, Rosa Maria Ortiz12, Juan J Lence-Anta12, Celia María Pereda12, Daniel F Comiskey13, Huiling He13, Sandya Liyanarachchi13, Albert de la Chapelle13, Rossella Elisei14, Federica Gemignani15, Hauke Thomsen16,17, Asta Forsti16,18,19, Anthony F Herzig20, Anne-Louise Leutenegger21, Carole Rubino3, Evgenia Ostroumova22, Ausrele Kesminiene22, Marie-Christine Boutron-Ruault1, Jean-François Deleuze5, Pascal Guénel1, Florent de Vathaire3.   

Abstract

Incidence of differentiated thyroid carcinoma (DTC) varies considerably between ethnic groups, with particularly high incidence rates in Pacific Islanders. DTC is one of the cancers with the highest familial risk suggesting a major role of genetic risk factors, but only few susceptibility loci were identified so far. In order to assess the contribution of known DTC susceptibility loci and to identify new ones, we conducted a multiethnic genome-wide association study (GWAS) in individuals of European ancestry and of Oceanian ancestry from Pacific Islands. Our study included 1554 cases/1973 controls of European ancestry and 301 cases/348 controls of Oceanian ancestry from seven population-based case-control studies participating to the EPITHYR consortium. All participants were genotyped using the OncoArray-500K Beadchip (Illumina). We confirmed the association with the known DTC susceptibility loci at 2q35, 8p12, 9q22.33 and 14q13.3 in the European ancestry population and suggested two novel signals at 1p31.3 and 16q23.2, which were associated with thyroid-stimulating hormone levels in previous GWAS. We additionally replicated an association with 5p15.33 reported previously in Chinese and European populations. Except at 1p31.3, all associations were in the same direction in the population of Oceanian ancestry. We also observed that the frequencies of risk alleles at 2q35, 5p15.33 and 16q23.2 were significantly higher in Oceanians than in Europeans. However, additional GWAS and epidemiological studies in Oceanian populations are needed to fully understand the highest incidence observed in these populations.
© 2021 UICC.

Entities:  

Keywords:  case-control study; genome-wide association study; thyroid cancer

Year:  2021        PMID: 33527407     DOI: 10.1002/ijc.33488

Source DB:  PubMed          Journal:  Int J Cancer        ISSN: 0020-7136            Impact factor:   7.396


  2 in total

1.  Gene network and biological pathways associated with susceptibility to differentiated thyroid carcinoma.

Authors:  Thérèse Truong; Fabienne Lesueur; Om Kulkarni; Pierre-Emmanuel Sugier; Julie Guibon; Anne Boland-Augé; Christine Lonjou; Delphine Bacq-Daian; Robert Olaso; Carole Rubino; Vincent Souchard; Frédérique Rachedi; Juan Jesus Lence-Anta; Rosa Maria Ortiz; Constance Xhaard; Pierre Laurent-Puig; Claire Mulot; Anne-Valérie Guizard; Claire Schvartz; Marie-Christine Boutron-Ruault; Evgenia Ostroumova; Ausrele Kesminiene; Jean-François Deleuze; Pascal Guénel; Florent De Vathaire
Journal:  Sci Rep       Date:  2021-04-26       Impact factor: 4.379

2.  Leveraging pleiotropic association using sparse group variable selection in genomics data.

Authors:  Matthew Sutton; Pierre-Emmanuel Sugier; Therese Truong; Benoit Liquet
Journal:  BMC Med Res Methodol       Date:  2022-01-07       Impact factor: 4.615

  2 in total

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