A multi-stage genome-wide association study of bladder cancer identifies multiple susceptibility loci

We conducted a multi-stage, genome-wide association study of bladder cancer with a primary scan of 591,637 SNPs in 3,532 affected individuals (cases) and 5,120 controls of European descent from five studies followed by a replication strategy, which included 8,382 cases and 48,275 controls from 16 st...

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Authors: Rothman, Nathaniel; Real, Francisco X.; Serra, Consol; Lloreta, Josep, 1958-; Chanock, Stephen J.
Format: Article
Status:Accepted version
Publication date:2010
Country:España
Institution:Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya)
Repository:Recercat. Dipósit de la Recerca de Catalunya
OAI Identifier:oai:recercat.cat:10230/36598
Online Access:http://hdl.handle.net/10230/36598
http://dx.doi.org/10.1038/ng.687
Access Level:Open access
Keyword:Bladder cancer
Genome-wide association studies
Psychology
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author Rothman, Nathaniel
author2 Real, Francisco X.
Serra, Consol
Lloreta, Josep, 1958-
Chanock, Stephen J.
author2_role author
author
author
author
author_browse Chanock, Stephen J.
Lloreta, Josep, 1958-
Real, Francisco X.
Rothman, Nathaniel
Serra, Consol
author_facet Rothman, Nathaniel
Real, Francisco X.
Serra, Consol
Lloreta, Josep, 1958-
Chanock, Stephen J.
author_role author
collection Recercat. Dipósit de la Recerca de Catalunya
description We conducted a multi-stage, genome-wide association study of bladder cancer with a primary scan of 591,637 SNPs in 3,532 affected individuals (cases) and 5,120 controls of European descent from five studies followed by a replication strategy, which included 8,382 cases and 48,275 controls from 16 studies. In a combined analysis, we identified three new regions associated with bladder cancer on chromosomes 22q13.1, 19q12 and 2q37.1: rs1014971, (P = 8 × 10⁻¹²) maps to a non-genic region of chromosome 22q13.1, rs8102137 (P = 2 × 10⁻¹¹) on 19q12 maps to CCNE1 and rs11892031 (P = 1 × 10⁻⁷) maps to the UGT1A cluster on 2q37.1. We confirmed four previously identified genome-wide associations on chromosomes 3q28, 4p16.3, 8q24.21 and 8q24.3, validated previous candidate associations for the GSTM1 deletion (P = 4 × 10⁻¹¹) and a tag SNP for NAT2 acetylation status (P = 4 × 10⁻¹¹), and found interactions with smoking in both regions. Our findings on common variants associated with bladder cancer risk should provide new insights into the mechanisms of carcinogenesis.
eu_rights_str_mv openAccess
format article
id ES_2aba3dc99291cc883ccfa77d4e8f97fb
institution Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya)
instname_str Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya)
network_acronym_str ES
network_name_str España
oai_identifier_str oai:recercat.cat:10230/36598
publishDate 2010
publishDateSort 2010
publisher Nature Research
publisherStr Nature Research
reponame_str Recercat. Dipósit de la Recerca de Catalunya
spelling A multi-stage genome-wide association study of bladder cancer identifies multiple susceptibility loci Rothman, Nathaniel Real, Francisco X. Serra, Consol Lloreta, Josep, 1958- Chanock, Stephen J. Bladder cancer Genome-wide association studies Psychology We conducted a multi-stage, genome-wide association study of bladder cancer with a primary scan of 591,637 SNPs in 3,532 affected individuals (cases) and 5,120 controls of European descent from five studies followed by a replication strategy, which included 8,382 cases and 48,275 controls from 16 studies. In a combined analysis, we identified three new regions associated with bladder cancer on chromosomes 22q13.1, 19q12 and 2q37.1: rs1014971, (P = 8 × 10⁻¹²) maps to a non-genic region of chromosome 22q13.1, rs8102137 (P = 2 × 10⁻¹¹) on 19q12 maps to CCNE1 and rs11892031 (P = 1 × 10⁻⁷) maps to the UGT1A cluster on 2q37.1. We confirmed four previously identified genome-wide associations on chromosomes 3q28, 4p16.3, 8q24.21 and 8q24.3, validated previous candidate associations for the GSTM1 deletion (P = 4 × 10⁻¹¹) and a tag SNP for NAT2 acetylation status (P = 4 × 10⁻¹¹), and found interactions with smoking in both regions. Our findings on common variants associated with bladder cancer risk should provide new insights into the mechanisms of carcinogenesis. Nature Research http://hdl.handle.net/10230/36598 http://dx.doi.org/10.1038/ng.687
spellingShingle A multi-stage genome-wide association study of bladder cancer identifies multiple susceptibility loci
Rothman, Nathaniel
Bladder cancer
Genome-wide association studies
Psychology
status_str acceptedVersion
title A multi-stage genome-wide association study of bladder cancer identifies multiple susceptibility loci
title_full A multi-stage genome-wide association study of bladder cancer identifies multiple susceptibility loci
title_fullStr A multi-stage genome-wide association study of bladder cancer identifies multiple susceptibility loci
title_full_unstemmed A multi-stage genome-wide association study of bladder cancer identifies multiple susceptibility loci
title_short A multi-stage genome-wide association study of bladder cancer identifies multiple susceptibility loci
title_sort A multi-stage genome-wide association study of bladder cancer identifies multiple susceptibility loci
topic Bladder cancer
Genome-wide association studies
Psychology
topic_facet Bladder cancer
Genome-wide association studies
Psychology
url http://hdl.handle.net/10230/36598
http://dx.doi.org/10.1038/ng.687