Variation at 3p24.1 and 6q23.3 influences the risk of Hodgkin's lymphoma.
Variation at 3p24.1 and 6q23.3 influences the risk of Hodgkin's lymphoma.
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DOI:
10.1038/ncomms3549
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发表时间:
2013
影响因子:
16.6
通讯作者:
Houlston, Richard S.
中科院分区:
文献类型:
--
作者:
Frampton, Matthew;da Silva Filho, Miguel Inacio;Broderick, Peter;Thomsen, Hauke;Foersti, Asta;Vijayakrishnan, Jayaram;Cooke, Rosie;Enciso-Mora, Victor;Hoffmann, Per;Noethen, Markus M.;Lloyd, Amy;Holroyd, Amy;Eisele, Lewin;Joeckel, Karl-Heinz;Ponader, Sabine;von Strandmann, Elke Pogge;Lightfoot, Tracy;Roman, Eve;Lake, Annette;Montgomery, Dorothy;Jarrett, Ruth F.;Swerdlow, Anthony J.;Engert, Andreas;Hemminki, Kari;Houlston, Richard S.
In addition to HLA, recent genome-wide association studies (GWASs) of Hodgkin’s Lymphoma (HL) have identified susceptibility loci for HL at 2p16.1, 8q24.21 and 10p14. In this study, we perform a GWAS meta-analysis with published GWAS (totaling 1,465 cases and 6,417 controls of European background), and follow up the most significant association signals in 2,024 cases and 1,853 controls. A combined analysis identifies new HL susceptibility loci mapping to 3p24.1 (rs3806624; P=1.14×10-12, odds ratio [OR]=1.26) and 6q23.3 (rs7745098; P=3.42×10-9, OR=1.21). rs3806624 localizes 5’ to the EOMES (eomesodermin) gene within a p53 response element affecting p53 binding. rs7745098 maps intergenic to HBS1L and MYB, a region previously associated with hematopoiesis. These findings provide further insight into the genetic and biological basis of inherited susceptibility to HL.
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