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Genome-wide association study identifies multiple susceptibility loci for diffuse large B cell lymphoma
JR. Cerhan, SI. Berndt, J. Vijai, H. Ghesquières, J. McKay, SS. Wang, Z. Wang, M. Yeager, L. Conde, PI. de Bakker, A. Nieters, D. Cox, L. Burdett, A. Monnereau, CR. Flowers, AJ. De Roos, AR. Brooks-Wilson, Q. Lan, G. Severi, M. Melbye, J. Gu, RD....
Nature genetics.
2014 ;
46 (11) :
1233-8.
Jazyk angličtina Země Spojené státy americké
Typ dokumentu časopisecké články, metaanalýza, Research Support, N.I.H., Intramural
Perzistentní odkaz
https://www.medvik.cz/link/bmc15014046
Online
Plný text
NLK
ProQuest Central
od 2000-01-01 do Před 1 rokem
Medline Complete (EBSCOhost)
od 1998-06-01 do 2015-11-30
Health & Medicine (ProQuest)
od 2000-01-01 do Před 1 rokem
Public Health Database (ProQuest)
od 2000-01-01 do Před 1 rokem
PubMed
25261932
DOI
10.1038/ng.3105
Knihovny.cz E-zdroje
- MeSH
- běloši genetika MeSH
- celogenomová asociační studie MeSH
- difúzní velkobuněčný B-lymfom genetika MeSH
- genetická predispozice k nemoci genetika MeSH
- genetické lokusy genetika MeSH
- genotyp MeSH
- jednonukleotidový polymorfismus genetika MeSH
- lidé MeSH
- lokus kvantitativního znaku genetika MeSH
- mapování chromozomů MeSH
- pravděpodobnostní funkce MeSH
- výpočetní biologie MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- metaanalýza MeSH
- Research Support, N.I.H., Intramural MeSH
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.
] Unit of Infections and Cancer Barcelona Spain
Center for Chronic Immunodeficiency University Medical Center Freiburg Freiburg Germany
Centre Heni Becquerel Rouen France
Centre National de Génotypage Evry France
Danish Cancer Society Research Center Copenhagen Denmark
Department of Biomedical Science University of Cagliari Monserrato Italy
Department of Biostatistics University of Alabama at Birmingham Birmingham Alabama USA
Department of Biostatistics Yale School of Public Health New Haven Connecticut USA
Department of Cancer Etiology City of Hope Beckman Research Institute Duarte California USA
Department of Chronic Disease Prevention National Institute for Health and Welfare Helsinki Finland
Department of Environmental Health Sciences Yale School of Public Health New Haven Connecticut USA
Department of Epidemiology German Institute for Human Nutrition Potsdam Germany
Department of Epidemiology Harvard School of Public Health Boston Massachusetts USA
Department of Epidemiology MD Anderson Cancer Center Houston Texas USA
Department of Family Medicine and Public Health Sciences Wayne State University Detroit Michigan USA
Department of Health Sciences Research Mayo Clinic Rochester Minnesota USA
Department of Health Sciences University of York York UK
Department of Health Studies University of Chicago Chicago Illinois USA
Department of Hematology Centre Hospitalier Universitaire Henri Mondor Creteil France
Department of Internal Medicine Carver College of Medicine The University of Iowa Iowa City Iowa USA
Department of Medicine Mayo Clinic Rochester Minnesota USA
Department of Medicine Memorial Sloan Kettering Cancer Center New York New York USA
Department of Medicine Solna Karolinska Institutet Stockholm Sweden
Department of Pathology City of Hope National Medical Center Duarte California USA
Department of Pathology University of Melbourne Parkville Victoria Australia
Department of Public Health Clinical and Molecular Medicine University of Cagliari Monserrato Italy
Division of Biomedical Statistics and Informatics Mayo Clinic Jacksonville Florida USA
Division of Cancer Epidemiology and Genetics National Cancer Institute Bethesda Maryland USA
Division of Cancer Epidemiology German Cancer Research Center Heidelberg Germany
Division of Endocrinology Diabetes and Metabolism Ohio State University Columbus Ohio USA
Division of Public Health Sciences Fred Hutchinson Cancer Research Center Seattle Washington USA
Dongguk University Seoul Seoul South Korea
Epidemiology Research Program American Cancer Society Atlanta Georgia USA
Health Studies Sector Westat Rockville Maryland USA
Hematology Unit Ospedale Oncologico di Riferimento Regionale A Businco Cagliari Italy
Prince of Wales Clinical School University of New South Wales Sydney New South Wales Australia
School of Nursing and Human Sciences Dublin City University Dublin Ireland
School of Public Health Imperial College London London UK
Sydney School of Public Health University of Sydney Sydney New South Wales Australia
Tisch Cancer Institute Icahn School of Medicine at Mount Sinai New York New York USA
Winship Cancer Institute Emory University School of Medicine Atlanta Georgia USA
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- 700 1_
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- 700 1_
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- 700 1_
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- 700 1_
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- 700 1_
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- 700 1_
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- 700 1_
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- 700 1_
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