Abstract
Several chronic lymphocytic leukaemia (CLL) susceptibility loci have been reported; however, much of the heritable risk remains unidentified. Here we perform a meta-analysis of six genome-wide association studies, imputed using a merged reference panel of 1,000 Genomes and UK10K data, totalling 6,200 cases and 17,598 controls after replication. We identify nine risk loci at 1p36.11 (rs34676223, P=5.04 × 10-13), 1q42.13 (rs41271473, P=1.06 × 10-10), 4q24 (rs71597109, P=1.37 × 10 -10), 4q35.1 (rs57214277, P=3.69 × 10-8), 6p21.31 (rs3800461, P=1.97 × 10-8), 11q23.2 (rs61904987, P=2.64 × 10-11), 18q21.1 (rs1036935, P=3.27 × 10-8), 19p13.3 (rs7254272, P=4.67 × 10-8) and 22q13.33 (rs140522, P=2.70 × 10-9). These new and established risk loci map to areas of active chromatin and show an over-representation of transcription factor binding for the key determinants of B-cell development and immune response.
Originalsprog | Engelsk |
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Artikelnummer | 14175 |
Tidsskrift | Nature Communications |
Vol/bind | 8 |
ISSN | 2041-1723 |
DOI | |
Status | Udgivet - 2017 |
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Genome-wide association analysis implicates dysregulation of immunity genes in chronic lymphocytic leukaemia. / Law, Philip J.; Berndt, Sonja I.; Speedy, Helen E.; Camp, Nicola J.; Sava, Georgina P.; Skibola, Christine F.; Holroyd, Amy; Joseph, Vijai; Sunter, Nicola J.; Nieters, Alexandra; Bea, Silvia; Monnereau, Alain; Martin-Garcia, David; Goldin, Lynn R.; Clot, Guillem; Teras, Lauren R.; Quintela, Inés; Birmann, Brenda M.; Jayne, Sandrine; Cozen, Wendy; Majid, Aneela; Smedby, Karin E.; Lan, Qing; Dearden, Claire; Brooks-Wilson, Angela R.; Hall, Andrew G.; Purdue, Mark P.; Mainou-Fowler, Tryfonia; Vajdic, Claire M.; Jackson, Graham H.; Cocco, Pierluigi; Marr, Helen; Zhang, Yawei; Zheng, Tongzhang; Giles, Graham G.; Lawrence, Charles; Call, Timothy G.; Liebow, Mark; Melbye, Mads; Glimelius, Bengt; Mansouri, Larry; Glenn, Martha; Curtin, Karen; Diver, W. Ryan; Link, Brian K.; Conde, Lucia; Bracci, Paige M.; Holly, Elizabeth A.; Jackson, Rebecca D.; Tinker, Lesley F.; Benavente, Yolanda; Boffetta, Paolo; Brennan, Paul; Maynadie, Marc; McKay, James; Albanes, Demetrius; Weinstein, Stephanie; Wang, Zhaoming; Caporaso, Neil E.; Morton, Lindsay M.; Severson, Richard K.; Riboli, Elio; Vineis, Paolo; Vermeulen, Roel C.H.; Southey, Melissa C.; Milne, Roger L.; Clavel, Jacqueline; Topka, Sabine; Spinelli, John J.; Kraft, Peter; Ennas, Maria Grazia; Summerfield, Geoffrey; Ferri, Giovanni M.; Harris, Robert J.; Miligi, Lucia; Pettitt, Andrew R.; North, Kari E.; Allsup, David J.; Fraumeni, Joseph F.; Bailey, James R.; Offit, Kenneth; Pratt, Guy; Hjalgrim, Henrik; Pepper, Chris; Chanock, Stephen J.; Fegan, Chris; Rosenquist, Richard; De Sanjose, Silvia; Carracedo, Angel; Dyer, Martin J.S.; Catovsky, Daniel; Campo, Elias; Cerhan, James R.; Allan, James M.; Rothman, Nathanial; Houlston, Richard; Slager, Susan.
I: Nature Communications, Bind 8, 14175, 2017.Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › peer review
}
TY - JOUR
T1 - Genome-wide association analysis implicates dysregulation of immunity genes in chronic lymphocytic leukaemia
AU - Law, Philip J.
AU - Berndt, Sonja I.
AU - Speedy, Helen E.
AU - Camp, Nicola J.
AU - Sava, Georgina P.
AU - Skibola, Christine F.
AU - Holroyd, Amy
AU - Joseph, Vijai
AU - Sunter, Nicola J.
AU - Nieters, Alexandra
AU - Bea, Silvia
AU - Monnereau, Alain
AU - Martin-Garcia, David
AU - Goldin, Lynn R.
AU - Clot, Guillem
AU - Teras, Lauren R.
AU - Quintela, Inés
AU - Birmann, Brenda M.
AU - Jayne, Sandrine
AU - Cozen, Wendy
AU - Majid, Aneela
AU - Smedby, Karin E.
AU - Lan, Qing
AU - Dearden, Claire
AU - Brooks-Wilson, Angela R.
AU - Hall, Andrew G.
AU - Purdue, Mark P.
AU - Mainou-Fowler, Tryfonia
AU - Vajdic, Claire M.
AU - Jackson, Graham H.
AU - Cocco, Pierluigi
AU - Marr, Helen
AU - Zhang, Yawei
AU - Zheng, Tongzhang
AU - Giles, Graham G.
AU - Lawrence, Charles
AU - Call, Timothy G.
AU - Liebow, Mark
AU - Melbye, Mads
AU - Glimelius, Bengt
AU - Mansouri, Larry
AU - Glenn, Martha
AU - Curtin, Karen
AU - Diver, W. Ryan
AU - Link, Brian K.
AU - Conde, Lucia
AU - Bracci, Paige M.
AU - Holly, Elizabeth A.
AU - Jackson, Rebecca D.
AU - Tinker, Lesley F.
AU - Benavente, Yolanda
AU - Boffetta, Paolo
AU - Brennan, Paul
AU - Maynadie, Marc
AU - McKay, James
AU - Albanes, Demetrius
AU - Weinstein, Stephanie
AU - Wang, Zhaoming
AU - Caporaso, Neil E.
AU - Morton, Lindsay M.
AU - Severson, Richard K.
AU - Riboli, Elio
AU - Vineis, Paolo
AU - Vermeulen, Roel C.H.
AU - Southey, Melissa C.
AU - Milne, Roger L.
AU - Clavel, Jacqueline
AU - Topka, Sabine
AU - Spinelli, John J.
AU - Kraft, Peter
AU - Ennas, Maria Grazia
AU - Summerfield, Geoffrey
AU - Ferri, Giovanni M.
AU - Harris, Robert J.
AU - Miligi, Lucia
AU - Pettitt, Andrew R.
AU - North, Kari E.
AU - Allsup, David J.
AU - Fraumeni, Joseph F.
AU - Bailey, James R.
AU - Offit, Kenneth
AU - Pratt, Guy
AU - Hjalgrim, Henrik
AU - Pepper, Chris
AU - Chanock, Stephen J.
AU - Fegan, Chris
AU - Rosenquist, Richard
AU - De Sanjose, Silvia
AU - Carracedo, Angel
AU - Dyer, Martin J.S.
AU - Catovsky, Daniel
AU - Campo, Elias
AU - Cerhan, James R.
AU - Allan, James M.
AU - Rothman, Nathanial
AU - Houlston, Richard
AU - Slager, Susan
PY - 2017
Y1 - 2017
N2 - Several chronic lymphocytic leukaemia (CLL) susceptibility loci have been reported; however, much of the heritable risk remains unidentified. Here we perform a meta-analysis of six genome-wide association studies, imputed using a merged reference panel of 1,000 Genomes and UK10K data, totalling 6,200 cases and 17,598 controls after replication. We identify nine risk loci at 1p36.11 (rs34676223, P=5.04 × 10-13), 1q42.13 (rs41271473, P=1.06 × 10-10), 4q24 (rs71597109, P=1.37 × 10 -10), 4q35.1 (rs57214277, P=3.69 × 10-8), 6p21.31 (rs3800461, P=1.97 × 10-8), 11q23.2 (rs61904987, P=2.64 × 10-11), 18q21.1 (rs1036935, P=3.27 × 10-8), 19p13.3 (rs7254272, P=4.67 × 10-8) and 22q13.33 (rs140522, P=2.70 × 10-9). These new and established risk loci map to areas of active chromatin and show an over-representation of transcription factor binding for the key determinants of B-cell development and immune response.
AB - Several chronic lymphocytic leukaemia (CLL) susceptibility loci have been reported; however, much of the heritable risk remains unidentified. Here we perform a meta-analysis of six genome-wide association studies, imputed using a merged reference panel of 1,000 Genomes and UK10K data, totalling 6,200 cases and 17,598 controls after replication. We identify nine risk loci at 1p36.11 (rs34676223, P=5.04 × 10-13), 1q42.13 (rs41271473, P=1.06 × 10-10), 4q24 (rs71597109, P=1.37 × 10 -10), 4q35.1 (rs57214277, P=3.69 × 10-8), 6p21.31 (rs3800461, P=1.97 × 10-8), 11q23.2 (rs61904987, P=2.64 × 10-11), 18q21.1 (rs1036935, P=3.27 × 10-8), 19p13.3 (rs7254272, P=4.67 × 10-8) and 22q13.33 (rs140522, P=2.70 × 10-9). These new and established risk loci map to areas of active chromatin and show an over-representation of transcription factor binding for the key determinants of B-cell development and immune response.
U2 - 10.1038/ncomms14175
DO - 10.1038/ncomms14175
M3 - Journal article
C2 - 28165464
AN - SCOPUS:85012025522
VL - 8
JO - Nature Communications
JF - Nature Communications
SN - 2041-1723
M1 - 14175
ER -