Genome-wide association study identifies multiple susceptibility loci for diffuse large B cell lymphoma
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Genome-wide association study identifies multiple susceptibility loci for diffuse large B cell lymphoma. / Cerhan, James R.; Berndt, Sonja I.; Vijai, Joseph; Ghesquières, Hervé; McKay, James; Wang, Sophia S.; Wang, Zhaoming; Yeager, Meredith; Conde, Lucia; De Bakker, Paul I.W.; Nieters, Alexandra; Cox, David; Burdett, Laurie; Monnereau, Alain; Flowers, Christopher R.; De Roos, Anneclaire J.; Brooks-Wilson, Angela R.; Lan, Qing; Severi, Gianluca; Melbye, Mads; Gu, Jian; Jackson, Rebecca D.; Kane, Eleanor; Teras, Lauren R.; Purdue, Mark P.; Vajdic, Claire M.; Spinelli, John J.; Giles, Graham G.; Albanes, Demetrius; Kelly, Rachel S.; Zucca, Mariagrazia; Bertrand, Kimberly A.; Zeleniuch-Jacquotte, Anne; Lawrence, Charles; Hutchinson, Amy; Zhi, Degui; Habermann, Thomas M.; Link, Brian K.; Novak, Anne J.; Dogan, Ahmet; Asmann, Yan W.; Liebow, Mark; Thompson, Carrie A.; Ansell, Stephen M.; Witzig, Thomas E.; Weiner, George J.; Veron, Amelie S.; Zelenika, Diana; Hjalgrim, Henrik; Tjonneland, Anne.
In: Nature Genetics, Vol. 46, No. 11, 05.11.2014, p. 1233-1238.Research output: Contribution to journal › Journal article › Research › peer-review
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TY - JOUR
T1 - Genome-wide association study identifies multiple susceptibility loci for diffuse large B cell lymphoma
AU - Cerhan, James R.
AU - Berndt, Sonja I.
AU - Vijai, Joseph
AU - Ghesquières, Hervé
AU - McKay, James
AU - Wang, Sophia S.
AU - Wang, Zhaoming
AU - Yeager, Meredith
AU - Conde, Lucia
AU - De Bakker, Paul I.W.
AU - Nieters, Alexandra
AU - Cox, David
AU - Burdett, Laurie
AU - Monnereau, Alain
AU - Flowers, Christopher R.
AU - De Roos, Anneclaire J.
AU - Brooks-Wilson, Angela R.
AU - Lan, Qing
AU - Severi, Gianluca
AU - Melbye, Mads
AU - Gu, Jian
AU - Jackson, Rebecca D.
AU - Kane, Eleanor
AU - Teras, Lauren R.
AU - Purdue, Mark P.
AU - Vajdic, Claire M.
AU - Spinelli, John J.
AU - Giles, Graham G.
AU - Albanes, Demetrius
AU - Kelly, Rachel S.
AU - Zucca, Mariagrazia
AU - Bertrand, Kimberly A.
AU - Zeleniuch-Jacquotte, Anne
AU - Lawrence, Charles
AU - Hutchinson, Amy
AU - Zhi, Degui
AU - Habermann, Thomas M.
AU - Link, Brian K.
AU - Novak, Anne J.
AU - Dogan, Ahmet
AU - Asmann, Yan W.
AU - Liebow, Mark
AU - Thompson, Carrie A.
AU - Ansell, Stephen M.
AU - Witzig, Thomas E.
AU - Weiner, George J.
AU - Veron, Amelie S.
AU - Zelenika, Diana
AU - Hjalgrim, Henrik
AU - Tjonneland, Anne
PY - 2014/11/5
Y1 - 2014/11/5
N2 - Diffuse large B cell lymphoma (DLBCL) is the most common lymphoma subtype and is clinically aggressive. To identify genetic susceptibility loci for DLBCL, we conducted a meta-analysis of 3 new genome-wide association studies (GWAS) and 1 previous scan, totaling 3,857 cases and 7,666 controls of European ancestry, with additional genotyping of 9 promising SNPs in 1,359 cases and 4,557 controls. In our multi-stage analysis, five independent SNPs in four loci achieved genome-wide significance marked by rs116446171 at 6p25.3 (EXOC2; P = 2.33 × 10 '21), rs2523607 at 6p21.33 (HLA-B; P = 2.40 × 10 '10), rs79480871 at 2p23.3 (NCOA1; P = 4.23 × 10 '8) and two independent SNPs, rs13255292 and rs4733601, at 8q24.21 (PVT1; P = 9.98 × 10 '13 and 3.63 × 10 '11, respectively). These data provide substantial new evidence for genetic susceptibility to this B cell malignancy and point to pathways involved in immune recognition and immune function in the pathogenesis of DLBCL.
AB - Diffuse large B cell lymphoma (DLBCL) is the most common lymphoma subtype and is clinically aggressive. To identify genetic susceptibility loci for DLBCL, we conducted a meta-analysis of 3 new genome-wide association studies (GWAS) and 1 previous scan, totaling 3,857 cases and 7,666 controls of European ancestry, with additional genotyping of 9 promising SNPs in 1,359 cases and 4,557 controls. In our multi-stage analysis, five independent SNPs in four loci achieved genome-wide significance marked by rs116446171 at 6p25.3 (EXOC2; P = 2.33 × 10 '21), rs2523607 at 6p21.33 (HLA-B; P = 2.40 × 10 '10), rs79480871 at 2p23.3 (NCOA1; P = 4.23 × 10 '8) and two independent SNPs, rs13255292 and rs4733601, at 8q24.21 (PVT1; P = 9.98 × 10 '13 and 3.63 × 10 '11, respectively). These data provide substantial new evidence for genetic susceptibility to this B cell malignancy and point to pathways involved in immune recognition and immune function in the pathogenesis of DLBCL.
U2 - 10.1038/ng.3105
DO - 10.1038/ng.3105
M3 - Journal article
C2 - 25261932
AN - SCOPUS:84908886283
VL - 46
SP - 1233
EP - 1238
JO - Nature Genetics
JF - Nature Genetics
SN - 1061-4036
IS - 11
ER -
ID: 257835831