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

Lin, W-Y; Fordham, SE; Hungate, E; Sunter, NJ; Elstob, C; Xu, Y; Park, C; ... Allan, JM; + view all (2021) Genome-wide association study identifies susceptibility loci for acute myeloid leukemia. Nature Communications , 12 (1) , Article 6233. 10.1038/s41467-021-26551-x. Green open access

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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^{-8}; 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^{−10}; HLA). Our results inform on AML etiology and identify putative functional genes operating in histone methylation (KMT5B) and immune function (HLA).

Type: Article
Title: Genome-wide association study identifies susceptibility loci for acute myeloid leukemia
Location: England
Open access status: An open access version is available from UCL Discovery
DOI: 10.1038/s41467-021-26551-x
Publisher version: https://doi.org/10.1038/s41467-021-26551-x
Language: English
Additional information: © 2021 Springer Nature Limited. This article is licensed under a Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/).
UCL classification: UCL
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Medical Sciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Medical Sciences > Cancer Institute
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Medical Sciences > Cancer Institute > Research Department of Haematology
URI: https://discovery-pp.ucl.ac.uk/id/eprint/10138449
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