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HLA Class I and II Diversity Contributes to the Etiologic Heterogeneity of Non-Hodgkin Lymphoma Subtypes
SS. Wang, M. Carrington, SI. Berndt, SL. Slager, PM. Bracci, J. Voutsinas, JR. Cerhan, KE. Smedby, H. Hjalgrim, J. Vijai, LM. Morton, R. Vermeulen, O. Paltiel, CM. Vajdic, MS. Linet, A. Nieters, S. de Sanjose, W. Cozen, EE. Brown, J. Turner, JJ....
Jazyk angličtina Země Spojené státy americké
Typ dokumentu časopisecké články, Research Support, N.I.H., Extramural, Research Support, N.I.H., Intramural, práce podpořená grantem, Research Support, U.S. Gov't, Non-P.H.S., Research Support, U.S. Gov't, P.H.S.
Grantová podpora
CIHR - Canada
Cancer Research UK - United Kingdom
HHSN261201000140C
NCI NIH HHS - United States
R01 CA092153
NCI NIH HHS - United States
R01 CA149445
NCI NIH HHS - United States
P30 CA016087
NCI NIH HHS - United States
R01 CA049449
NCI NIH HHS - United States
R01 CA200703
NCI NIH HHS - United States
P30 CA042014
NCI NIH HHS - United States
N01CO12400
NCI NIH HHS - United States
R01 CA062006
NCI NIH HHS - United States
N01 PC067009
NCI NIH HHS - United States
HHSN261201000026C
NCI NIH HHS - United States
R01 CA098661
NCI NIH HHS - United States
P01 CA087969
NCI NIH HHS - United States
U01 HG007033
NHGRI NIH HHS - United States
U01 CA118444
NCI NIH HHS - United States
P30 CA086862
NCI NIH HHS - United States
R01 CA134674
NCI NIH HHS - United States
R01 CA148690
NCI NIH HHS - United States
HHSN261201000035I
NCI NIH HHS - United States
U01 CA167552
NCI NIH HHS - United States
P30 CA015083
NCI NIH HHS - United States
R03 CA179558
NCI NIH HHS - United States
HHSN261201500005C
NCI NIH HHS - United States
HHSN261201000034C
NCI NIH HHS - United States
HHSN261201000035C
NCI NIH HHS - United States
U58 DP000807
NCCDPHP CDC HHS - United States
UL1 TR000135
NCATS NIH HHS - United States
N01 PC067008
NCI NIH HHS - United States
R01 CA154643
NCI NIH HHS - United States
N01 PC067010
NCI NIH HHS - United States
HHSN261200800001C
CCR NIH HHS - United States
UM1 CA186107
NCI NIH HHS - United States
U01 CA049449
NCI NIH HHS - United States
K08 CA134919
NCI NIH HHS - United States
P30 ES000260
NIEHS NIH HHS - United States
UM1 CA167552
NCI NIH HHS - United States
R21 CA165923
NCI NIH HHS - United States
R01 CA098122
NCI NIH HHS - United States
N01 PC065064
NCI NIH HHS - United States
P50 CA097274
NCI NIH HHS - United States
P30 CA033572
NCI NIH HHS - United States
HHSN261200800001E
NCI NIH HHS - United States
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- MeSH
- celogenomová asociační studie metody MeSH
- genetická heterogenita MeSH
- heterozygot MeSH
- histokompatibilita - antigeny třídy I genetika MeSH
- histokompatibilita - antigeny třídy II genetika MeSH
- lidé MeSH
- nehodgkinský lymfom genetika MeSH
- prospektivní studie MeSH
- studie případů a kontrol MeSH
- Check Tag
- lidé MeSH
- mužské pohlaví MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Research Support, N.I.H., Extramural MeSH
- Research Support, N.I.H., Intramural MeSH
- Research Support, U.S. Gov't, Non-P.H.S. MeSH
- Research Support, U.S. Gov't, P.H.S. MeSH
A growing number of loci within the human leukocyte antigen (HLA) region have been implicated in non-Hodgkin lymphoma (NHL) etiology. Here, we test a complementary hypothesis of "heterozygote advantage" regarding the role of HLA and NHL, whereby HLA diversity is beneficial and homozygous HLA loci are associated with increased disease risk. HLA alleles at class I and II loci were imputed from genome-wide association studies (GWAS) using SNP2HLA for 3,617 diffuse large B-cell lymphomas (DLBCL), 2,686 follicular lymphomas (FL), 2,878 chronic lymphocytic leukemia/small lymphocytic lymphomas (CLL/SLL), 741 marginal zone lymphomas (MZL), and 8,753 controls of European descent. Both DLBCL and MZL risk were elevated with homozygosity at class I HLA-B and -C loci (OR DLBCL = 1.31, 95% CI = 1.06-1.60; OR MZL = 1.45, 95% CI = 1.12-1.89) and class II HLA-DRB1 locus (OR DLBCL = 2.10, 95% CI = 1.24-3.55; OR MZL = 2.10, 95% CI = 0.99-4.45). Increased FL risk was observed with the overall increase in number of homozygous HLA class II loci (P trend < 0.0001, FDR = 0.0005). These results support a role for HLA zygosity in NHL etiology and suggests that distinct immune pathways may underly the etiology of the different NHL subtypes.Significance: HLA gene diversity reduces risk for non-Hodgkin lymphoma. Cancer Res; 78(14); 4086-96. ©2018 AACR.
Bill Lyons Informatics Centre UCL Cancer Institute University College London London United Kingdom
Cancer Epidemiology and Intelligence Division Cancer Council Victoria Melbourne Australia
Cancer Epidemiology Unit University of Oxford Oxford United Kingdom
Cancer Research Center of Lyon INSERM UMR1052 Center Léon Bérard Lyon France
Department of Biomedical Science University of Cagliari Monserrato Cagliari Italy
Department of Epidemiology School of Public Health Brown University Providence Rhode Island
Department of Family Medicine and Public Health Sciences Wayne State University Detroit Michigan
Department of Health Sciences Research Mayo Clinic Rochester Minnesota
Department of Health Sciences University of York York United Kingdom
Department of Hematology and Medical Oncology Emory University School of Medicine Atlanta Georgia
Department of Hematology Rishospitalet Copenhagen Denmark
Department of Immunology CHU Henri Mondor Créteil France
Department of Immunology Genetics and Pathology Uppsala University Uppsala Sweden
Department of Internal Medicine Carver College of Medicine The University of Iowa Iowa City Iowa
Department of Laboratory Medicine and Pathology Mayo Clinic Rochester Minnesota
Department of Medical Epidemiology and Biostatistics Karolinska Institutet Stockholm Sweden
Department of Medicine Memorial Sloan Kettering Cancer Center New York City New York
Department of Pathology City of Hope Duarte California
Department of Population Sciences Beckman Research Institute and the City of Hope Duarte California
Department of Public Health Clinical and Molecular Medicine University of Cagliari Cagliari Italy
Division of Cancer Epidemiology and Genetics NCI Bethesda Maryland
Division of Clinical Epidemiology German Cancer Research Centre Heidelberg Baden Württemberg Germany
Division of Hematology S Francesco Hospital Nuoro Italy
Epidemiology Research Program American Cancer Society Atlanta Georgia
International Agency for Research on Cancer Lyon France
School of Nursing and Human Sciences Dublin City University Dublin Ireland
School of Public Health Imperial College London London United Kingdom
Sydney School of Public Health The University of Sydney Sydney Australia
The Tisch Cancer Institute Icahn School of Medicine at Mount Sinai New York City New York
Citace poskytuje Crossref.org
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- GRA __
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- GRA __
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- GRA __
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- GRA __
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- GRA __
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- GRA __
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- GRA __
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- GRA __
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- GRA __
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- GRA __
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- GRA __
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- GRA __
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- GRA __
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- GRA __
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- GRA __
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- GRA __
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- GRA __
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- GRA __
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- GRA __
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- GRA __
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- GRA __
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- GRA __
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- LZP __
- $a Pubmed-20191007