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Genome-wide association study identifies susceptibility loci for acute myeloid leukemia.

Authors :
Lin WY
Fordham SE
Hungate E
Sunter NJ
Elstob C
Xu Y
Park C
Quante A
Strauch K
Gieger C
Skol A
Rahman T
Sucheston-Campbell L
Wang J
Hahn T
Clay-Gilmour AI
Jones GL
Marr HJ
Jackson GH
Menne T
Collin M
Ivey A
Hills RK
Burnett AK
Russell NH
Fitzgibbon J
Larson RA
Le Beau MM
Stock W
Heidenreich O
Alharbi A
Allsup DJ
Houlston RS
Norden J
Dickinson AM
Douglas E
Lendrem C
Daly AK
Palm L
Piechocki K
Jeffries S
Bornhäuser M
Röllig C
Altmann H
Ruhnke L
Kunadt D
Wagenführ L
Cordell HJ
Darlay R
Andersen MK
Fontana MC
Martinelli G
Marconi G
Sanz MA
Cervera J
Gómez-Seguí I
Cluzeau T
Moreilhon C
Raynaud S
Sill H
Voso MT
Lo-Coco F
Dombret H
Cheok M
Preudhomme C
Gale RE
Linch D
Gaal-Wesinger J
Masszi A
Nowak D
Hofmann WK
Gilkes A
Porkka K
Milosevic Feenstra JD
Kralovics R
Grimwade D
Meggendorfer M
Haferlach T
Krizsán S
Bödör C
Stölzel F
Onel K
Allan JM
Source :
Nature communications [Nat Commun] 2021 Oct 29; Vol. 12 (1), pp. 6233. Date of Electronic Publication: 2021 Oct 29.
Publication Year :
2021

Abstract

Acute myeloid leukemia (AML) is a hematological malignancy with an undefined heritable risk. Here we perform a meta-analysis of three genome-wide association studies, with replication in a fourth study, incorporating a total of 4018 AML cases and 10488 controls. We identify a genome-wide significant risk locus for AML at 11q13.2 (rs4930561; P = 2.15 × 10 <superscript>-8</superscript> ; KMT5B). We also identify a genome-wide significant risk locus for the cytogenetically normal AML sub-group (N = 1287) at 6p21.32 (rs3916765; P = 1.51 × 10 <superscript>-10</superscript> ; HLA). Our results inform on AML etiology and identify putative functional genes operating in histone methylation (KMT5B) and immune function (HLA).<br /> (© 2021. The Author(s).)

Details

Language :
English
ISSN :
2041-1723
Volume :
12
Issue :
1
Database :
MEDLINE
Journal :
Nature communications
Publication Type :
Academic Journal
Accession number :
34716350
Full Text :
https://doi.org/10.1038/s41467-021-26551-x