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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

Genome-wide association (GWA) studies have thus far identified 10 loci at which common variants influence the risk of developing colorectal cancer (CRC). To enhance power to identify additional loci, we conducted a meta-analysis of three GWA studies from the UK totalling 3,334 cases and 4,628 contro...

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Detalles Bibliográficos
Autores principales: Houlston, Richard S, Cheadle, Jeremy, Dobbins, Sara E, Tenesa, Albert, Jones, Angela M, Howarth, Kimberley, Spain, Sarah L, Broderick, Peter, Domingo, Enric, Farrington, Susan, Prendergast, James GD, Pittman, Alan M, Theodoratou, Evi, Smith, Christopher G, Olver, Bianca, Walther, Axel, Barnetson, Rebecca A, Churchman, Michael, Jaeger, Emma EM, Penegar, Steven, Barclay, Ella, Martin, Lynn, Gorman, Maggie, Mager, Rachel, Johnstone, Elaine, Midgley, Rachel, Niittymäki, Iina, Tuupanen, Sari, Colley, James, Idziaszczyk, Shelley, Thomas, Huw JM, Lucassen, Anneke M, Evans, D Gareth R, Maher, Eamonn R, Maughan, Timothy, Dimas, Antigone, Dermitzakis, Emmanouil, Cazier, Jean-Baptiste, Aaltonen, Lauri A, Pharoah, Paul, Kerr, David J, Carvajal-Carmona, Luis G, Campbell, Harry, Dunlop, Malcolm G, Tomlinson, Ian PM
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5098601/
https://www.ncbi.nlm.nih.gov/pubmed/20972440
http://dx.doi.org/10.1038/ng.670
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author Houlston, Richard S
Cheadle, Jeremy
Dobbins, Sara E
Tenesa, Albert
Jones, Angela M
Howarth, Kimberley
Spain, Sarah L
Broderick, Peter
Domingo, Enric
Farrington, Susan
Prendergast, James GD
Pittman, Alan M
Theodoratou, Evi
Smith, Christopher G
Olver, Bianca
Walther, Axel
Barnetson, Rebecca A
Churchman, Michael
Jaeger, Emma EM
Penegar, Steven
Barclay, Ella
Martin, Lynn
Gorman, Maggie
Mager, Rachel
Johnstone, Elaine
Midgley, Rachel
Niittymäki, Iina
Tuupanen, Sari
Colley, James
Idziaszczyk, Shelley
Thomas, Huw JM
Lucassen, Anneke M
Evans, D Gareth R
Maher, Eamonn R
Maughan, Timothy
Dimas, Antigone
Dermitzakis, Emmanouil
Cazier, Jean-Baptiste
Aaltonen, Lauri A
Pharoah, Paul
Kerr, David J
Carvajal-Carmona, Luis G
Campbell, Harry
Dunlop, Malcolm G
Tomlinson, Ian PM
author_facet Houlston, Richard S
Cheadle, Jeremy
Dobbins, Sara E
Tenesa, Albert
Jones, Angela M
Howarth, Kimberley
Spain, Sarah L
Broderick, Peter
Domingo, Enric
Farrington, Susan
Prendergast, James GD
Pittman, Alan M
Theodoratou, Evi
Smith, Christopher G
Olver, Bianca
Walther, Axel
Barnetson, Rebecca A
Churchman, Michael
Jaeger, Emma EM
Penegar, Steven
Barclay, Ella
Martin, Lynn
Gorman, Maggie
Mager, Rachel
Johnstone, Elaine
Midgley, Rachel
Niittymäki, Iina
Tuupanen, Sari
Colley, James
Idziaszczyk, Shelley
Thomas, Huw JM
Lucassen, Anneke M
Evans, D Gareth R
Maher, Eamonn R
Maughan, Timothy
Dimas, Antigone
Dermitzakis, Emmanouil
Cazier, Jean-Baptiste
Aaltonen, Lauri A
Pharoah, Paul
Kerr, David J
Carvajal-Carmona, Luis G
Campbell, Harry
Dunlop, Malcolm G
Tomlinson, Ian PM
author_sort Houlston, Richard S
collection PubMed
description Genome-wide association (GWA) studies have thus far identified 10 loci at which common variants influence the risk of developing colorectal cancer (CRC). To enhance power to identify additional loci, we conducted a meta-analysis of three GWA studies from the UK totalling 3,334 cases and 4,628 controls, followed by multiple validation analyses, involving a total of 18,095 CRC cases and 20,197 controls. We identified new associations at 4 CRC risk loci: 1q41 (rs6691170, OR=1.06, P=9.55x10(-10); rs6687758, OR=1.09, P=2.27x10(-9)); 3q26.2 (rs10936599, OR=0.93, P=3.39x10(-8)); 12q13.13 (rs11169552, OR=0.92, P=1.89x10(-10); rs7136702, OR=1.06, P=4.02=x10(-8)); and 20q13.33 (rs4925386, OR=0.93, P=1.89x10(-10)). As well as identifying multiple new CRC risk loci this analysis provides evidence that additional CRC-associated variants of similar effect size remain to be discovered.
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spelling pubmed-50986012016-11-07 Meta-analysis of three genome-wide association studies identifies susceptibility loci for colorectal cancer at 1q41, 3q26.2, 12q13.13 and 20q13.33 Houlston, Richard S Cheadle, Jeremy Dobbins, Sara E Tenesa, Albert Jones, Angela M Howarth, Kimberley Spain, Sarah L Broderick, Peter Domingo, Enric Farrington, Susan Prendergast, James GD Pittman, Alan M Theodoratou, Evi Smith, Christopher G Olver, Bianca Walther, Axel Barnetson, Rebecca A Churchman, Michael Jaeger, Emma EM Penegar, Steven Barclay, Ella Martin, Lynn Gorman, Maggie Mager, Rachel Johnstone, Elaine Midgley, Rachel Niittymäki, Iina Tuupanen, Sari Colley, James Idziaszczyk, Shelley Thomas, Huw JM Lucassen, Anneke M Evans, D Gareth R Maher, Eamonn R Maughan, Timothy Dimas, Antigone Dermitzakis, Emmanouil Cazier, Jean-Baptiste Aaltonen, Lauri A Pharoah, Paul Kerr, David J Carvajal-Carmona, Luis G Campbell, Harry Dunlop, Malcolm G Tomlinson, Ian PM Nat Genet Article Genome-wide association (GWA) studies have thus far identified 10 loci at which common variants influence the risk of developing colorectal cancer (CRC). To enhance power to identify additional loci, we conducted a meta-analysis of three GWA studies from the UK totalling 3,334 cases and 4,628 controls, followed by multiple validation analyses, involving a total of 18,095 CRC cases and 20,197 controls. We identified new associations at 4 CRC risk loci: 1q41 (rs6691170, OR=1.06, P=9.55x10(-10); rs6687758, OR=1.09, P=2.27x10(-9)); 3q26.2 (rs10936599, OR=0.93, P=3.39x10(-8)); 12q13.13 (rs11169552, OR=0.92, P=1.89x10(-10); rs7136702, OR=1.06, P=4.02=x10(-8)); and 20q13.33 (rs4925386, OR=0.93, P=1.89x10(-10)). As well as identifying multiple new CRC risk loci this analysis provides evidence that additional CRC-associated variants of similar effect size remain to be discovered. 2010-10-24 2010-11 /pmc/articles/PMC5098601/ /pubmed/20972440 http://dx.doi.org/10.1038/ng.670 Text en Users may view, print, copy, download and text and datamine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Houlston, Richard S
Cheadle, Jeremy
Dobbins, Sara E
Tenesa, Albert
Jones, Angela M
Howarth, Kimberley
Spain, Sarah L
Broderick, Peter
Domingo, Enric
Farrington, Susan
Prendergast, James GD
Pittman, Alan M
Theodoratou, Evi
Smith, Christopher G
Olver, Bianca
Walther, Axel
Barnetson, Rebecca A
Churchman, Michael
Jaeger, Emma EM
Penegar, Steven
Barclay, Ella
Martin, Lynn
Gorman, Maggie
Mager, Rachel
Johnstone, Elaine
Midgley, Rachel
Niittymäki, Iina
Tuupanen, Sari
Colley, James
Idziaszczyk, Shelley
Thomas, Huw JM
Lucassen, Anneke M
Evans, D Gareth R
Maher, Eamonn R
Maughan, Timothy
Dimas, Antigone
Dermitzakis, Emmanouil
Cazier, Jean-Baptiste
Aaltonen, Lauri A
Pharoah, Paul
Kerr, David J
Carvajal-Carmona, Luis G
Campbell, Harry
Dunlop, Malcolm G
Tomlinson, Ian PM
Meta-analysis of three genome-wide association studies identifies susceptibility loci for colorectal cancer at 1q41, 3q26.2, 12q13.13 and 20q13.33
title Meta-analysis of three genome-wide association studies identifies susceptibility loci for colorectal cancer at 1q41, 3q26.2, 12q13.13 and 20q13.33
title_full Meta-analysis of three genome-wide association studies identifies susceptibility loci for colorectal cancer at 1q41, 3q26.2, 12q13.13 and 20q13.33
title_fullStr Meta-analysis of three genome-wide association studies identifies susceptibility loci for colorectal cancer at 1q41, 3q26.2, 12q13.13 and 20q13.33
title_full_unstemmed Meta-analysis of three genome-wide association studies identifies susceptibility loci for colorectal cancer at 1q41, 3q26.2, 12q13.13 and 20q13.33
title_short Meta-analysis of three genome-wide association studies identifies susceptibility loci for colorectal cancer at 1q41, 3q26.2, 12q13.13 and 20q13.33
title_sort meta-analysis of three genome-wide association studies identifies susceptibility loci for colorectal cancer at 1q41, 3q26.2, 12q13.13 and 20q13.33
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5098601/
https://www.ncbi.nlm.nih.gov/pubmed/20972440
http://dx.doi.org/10.1038/ng.670
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