| Literature DB >> 33527407 |
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.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