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Meta-analysis of three genome-wide association studies identifies susceptibility loci for colorectal cancer at 1q41, 3q26.2, 12q13.13 and 20q13.33.

Authors :
Houlston RS
Cheadle J
Dobbins SE
Tenesa A
Jones AM
Howarth K
Spain SL
Broderick P
Domingo E
Farrington S
Prendergast JG
Pittman AM
Theodoratou E
Smith CG
Olver B
Walther A
Barnetson RA
Churchman M
Jaeger EE
Penegar S
Barclay E
Martin L
Gorman M
Mager R
Johnstone E
Midgley R
Niittymäki I
Tuupanen S
Colley J
Idziaszczyk S
Thomas HJ
Lucassen AM
Evans DG
Maher ER
Maughan T
Dimas A
Dermitzakis E
Cazier JB
Aaltonen LA
Pharoah P
Kerr DJ
Carvajal-Carmona LG
Campbell H
Dunlop MG
Tomlinson IP
Source :
Nature genetics [Nat Genet] 2010 Nov; Vol. 42 (11), pp. 973-7. Date of Electronic Publication: 2010 Oct 24.
Publication Year :
2010

Abstract

Genome-wide association studies (GWAS) have identified ten loci harboring common variants that influence risk of developing colorectal cancer (CRC). To enhance the power to identify additional CRC risk loci, we conducted a meta-analysis of three GWAS from the UK which included a total of 3,334 affected individuals (cases) and 4,628 controls followed by multiple validation analyses including a total of 18,095 cases and 20,197 controls. We identified associations at four new CRC risk loci: 1q41 (rs6691170, odds ratio (OR) = 1.06, P = 9.55 × 10⁻¹⁰ and rs6687758, OR = 1.09, P = 2.27 × 10⁻⁹, 3q26.2 (rs10936599, OR = 0.93, P = 3.39 × 10⁻⁸), 12q13.13 (rs11169552, OR = 0.92, P = 1.89 × 10⁻¹⁰ and rs7136702, OR = 1.06, P = 4.02 × 10⁻⁸) and 20q13.33 (rs4925386, OR = 0.93, P = 1.89 × 10⁻¹⁰). In addition to identifying new CRC risk loci, this analysis provides evidence that additional CRC-associated variants of similar effect size remain to be discovered.<br />Competing Interests: statement The authors declare no competing financial interests.

Details

Language :
English
ISSN :
1546-1718
Volume :
42
Issue :
11
Database :
MEDLINE
Journal :
Nature genetics
Publication Type :
Academic Journal
Accession number :
20972440
Full Text :
https://doi.org/10.1038/ng.670