A genome-wide association study identifies multiple susceptibility loci for chronic lymphocytic leukemia

被引:161
作者
Speedy, Helen E. [1 ]
Di Bernardo, Maria Chiara [1 ]
Sava, Georgina P. [1 ]
Dyer, Martin J. S. [2 ]
Holroyd, Amy [1 ]
Wang, Yufei [1 ]
Sunter, Nicola J. [3 ]
Mansouri, Larry [4 ]
Juliusson, Gunnar [5 ]
Smedby, Karin E. [6 ]
Roos, Groan [7 ]
Jayne, Sandrine [8 ]
Majid, Aneela [8 ]
Dearden, Claire [9 ]
Hall, Andrew G. [3 ]
Mainou-Fowler, Tryfonia [10 ]
Jackson, Graham H. [11 ]
Summerfield, Geoffrey [12 ]
Harris, Robert J. [13 ]
Pettitt, Andrew R. [13 ]
Allsup, David J. [14 ]
Bailey, James R. [15 ,16 ]
Pratt, Guy [17 ]
Pepper, Chris [18 ]
Fegan, Chris [19 ]
Rosenquist, Richard [4 ]
Catovsky, Daniel [9 ]
Allan, James M. [3 ]
Houlston, Richard S. [1 ]
机构
[1] Inst Canc Res, Div Genet & Epidemiol, Sutton, Surrey, England
[2] Univ Leicester, Dept Canc Studies & Mol Med, Leicester, Leics, England
[3] Newcastle Univ, Northern Inst Canc Res, Newcastle Upon Tyne NE1 7RU, Tyne & Wear, England
[4] Uppsala Univ, Dept Immunol Genet & Pathol, Uppsala, Sweden
[5] Lund Univ, Lund Strateg Res Ctr Stem Cell Biol & Cell Therap, Lund, Sweden
[6] Karolinska Inst, Dept Med, Clin Epidemiol Unit, Stockholm, Sweden
[7] Umea Univ, Dept Med Biosci Pathol, Umea, Sweden
[8] Univ Leicester, Toxicol Unit, Med Res Council, Leicester, Leics, England
[9] Inst Canc Res, Div Mol Pathol, Sutton, Surrey, England
[10] Newcastle Univ, Sch Med, Newcastle Upon Tyne NE1 7RU, Tyne & Wear, England
[11] Royal Victoria Infirm, Dept Haematol, Newcastle Upon Tyne NE1 4LP, Tyne & Wear, England
[12] Queen Elizabeth Hosp, Dept Haematol, Newcastle Upon Tyne, Tyne & Wear, England
[13] Univ Liverpool, Dept Mol & Clin Canc Med, Liverpool L69 3BX, Merseyside, England
[14] Hull Royal Infirm, Dept Haematol, Kingston Upon Hull HU3 2JZ, N Humberside, England
[15] Hull York Med Sch, Kingston Upon Hull, N Humberside, England
[16] Univ Hull, Kingston Upon Hull HU6 7RX, N Humberside, England
[17] Birmingham Heartlands Hosp, Dept Haematol, Birmingham B9 5ST, W Midlands, England
[18] Cardiff Univ, Sch Med, Dept Haematol, Cardiff CF10 3AX, S Glam, Wales
[19] Cardiff & Vale Natl Hlth Serv Trust, Cardiff, S Glam, Wales
关键词
COLORECTAL-CANCER; TELOMERE LENGTH; CHROMATIN STATES; COMMON VARIATION; CELL-RECEPTOR; LUNG-CANCER; RISK; VARIANTS; PCR; METAANALYSIS;
D O I
10.1038/ng.2843
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Genome-wide association studies (GWAS) of chronic lymphocytic leukemia (CLL) have shown that common genetic variation contributes to the heritable risk of CLL. To identify additional CLL susceptibility loci, we conducted a GWAS and performed a meta-analysis with a published GWAS totaling 1,739 individuals with CLL (cases) and 5,199 controls with validation in an additional 1,144 cases and 3,151 controls. A combined analysis identified new susceptibility loci mapping to 3q26.2 (rs10936599, P = 1.74 x 10(-9)), 4q26 (rs6858698, P = 3.07 x 10(-9)), 6q25.2 (IPCEF1, rs2236256, P = 1.50 x 10(-10)) and 7q31.33 (POT1, rs17246404, P = 3.40 x 10(-8)). Additionally, we identified a promising association at 5p15.33 (CLPTM1L, rs31490, P = 1.72 x 10(-7)) and validated recently reported putative associations at 5p15.33 (TERT, rs10069690, P = 1.12 x 10(-10)) and 8q22.3 (rs2511714, P = 2.90 x 10(-9)). These findings provide further insights into the genetic and biological basis of inherited genetic susceptibility to CLL.
引用
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页码:56 / +
页数:7
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