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

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作者
Wei-Yu Lin
Sarah E. Fordham
Eric Hungate
Nicola J. Sunter
Claire Elstob
Yaobo Xu
Catherine Park
Anne Quante
Konstantin Strauch
Christian Gieger
Andrew Skol
Thahira Rahman
Lara Sucheston-Campbell
Junke Wang
Theresa Hahn
Alyssa I. Clay-Gilmour
Gail L. Jones
Helen J. Marr
Graham H. Jackson
Tobias Menne
Mathew Collin
Adam Ivey
Robert K. Hills
Alan K. Burnett
Nigel H. Russell
Jude Fitzgibbon
Richard A. Larson
Michelle M. Le Beau
Wendy Stock
Olaf Heidenreich
Abrar Alharbi
David J. Allsup
Richard S. Houlston
Jean Norden
Anne M. Dickinson
Elisabeth Douglas
Clare Lendrem
Ann K. Daly
Louise Palm
Kim Piechocki
Sally Jeffries
Martin Bornhäuser
Christoph Röllig
Heidi Altmann
Leo Ruhnke
Desiree Kunadt
Lisa Wagenführ
Heather J. Cordell
Rebecca Darlay
Mette K. Andersen
机构
[1] Newcastle University,Translational and Clinical Research Institute, Newcastle University Centre for Cancer, Faculty of Medical Sciences
[2] University of Chicago,Section of Pediatric Hematology and Oncology
[3] Helmholtz Zentrum München,Department of Medicine
[4] German Research Center for Environmental Health,Arnold School of Public Health, Department of Epidemiology & Biostatistics
[5] Ludwig-Maximilians-Universität München,Nuffield Department of Population Health
[6] Chair of Genetic Epidemiology,Translational and Clinical Research Institute, Faculty of Medical Sciences
[7] IBE,Department of Haematological Medicine
[8] Faculty of Medicine,Population Health Sciences Institute
[9] College of Pharmacy,Department of Clinical Genetics
[10] The Ohio State University,Institute of Hematology “L. and A. Seràgnoli”
[11] Roswell Park Cancer Institute,Hematology department
[12] University of South Carolina,Division of Hematology
[13] Department of Haematology,Department of Haematology
[14] Freeman Hospital,1st Department of Internal Medicine
[15] Newcastle upon Tyne Hospitals National Health Service Foundation Trust,3rd Department of Internal Medicine
[16] Department of Medical and Molecular Genetics,Department of Hematology and Oncology, Medical Faculty Mannheim
[17] King’s College Medical School,Department of Haematology
[18] University of Oxford,Helsinki University Hospital Comprehensive Cancer Center
[19] Paul O’Gorman Leukaemia Research Centre,Department of Laboratory Medicine
[20] University of Glasgow,HCEMM
[21] Department of Haematology,SE Molecular Oncohematology Research Group, 1st Department of Pathology and Experimental Cancer Research
[22] Nottingham University Hospitals NHS Trust,undefined
[23] Barts Cancer Institute,undefined
[24] Queen Mary University of London,undefined
[25] Centre for Atherothrombosis and Metabolic Disease,undefined
[26] Hull York Medical School,undefined
[27] Division of Genetics and Epidemiology,undefined
[28] The Institute of Cancer Research,undefined
[29] Newcastle University,undefined
[30] West Midlands Regional Genetics Laboratory,undefined
[31] Birmingham Women’s Hospital,undefined
[32] The Rayne Institute,undefined
[33] King’s College London,undefined
[34] National Center for Tumor Diseases NCT,undefined
[35] Partner site Dresden,undefined
[36] Medizinische Klinik und Poliklinik I,undefined
[37] University Hospital Carl Gustav Carus Dresden,undefined
[38] Technical University of Dresden,undefined
[39] Newcastle University,undefined
[40] University Hospital Rigshospitalet,undefined
[41] University of Bologna,undefined
[42] IRCCS Istituto Romagnolo per lo Studio dei Tumori (IRST) “Dino Amadori”,undefined
[43] Hematology Service,undefined
[44] Hospital Universitario y Politécnico La Fe,undefined
[45] CIBERONC,undefined
[46] Instituto de Salud Carlos III,undefined
[47] Cote d’Azur University,undefined
[48] CHU of Nice,undefined
[49] Medical University of Graz,undefined
[50] Università di Roma Tor Vergata,undefined
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摘要
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).
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    [J]. NATURE COMMUNICATIONS, 2021, 12 (01)
  • [2] Author Correction: Genome-wide association study identifies susceptibility loci for acute myeloid leukemia
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    Sarah E. Fordham
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