Common variation at 2q22.3 (ZEB2) influences the risk of renal cancer

Marc Henrion, Matthew Frampton, Ghislaine Scelo, Mark Purdue, Yuanqing Ye, Peter Broderick, Alastair Ritchie, Richard Kaplan, Angela Meade, James Mckay, Mattias Johansson, Mark Lathrop, James Larkin, Nathaniel Rothman, Zhaoming Wang, Wong Ho Chow, Victoria L. Stevens, W. Ryan Diver, Susan M. Gapstur, Demetrius AlbanesJarmo Virtamo, Xifeng Wu, Paul Brennan, Stephen Chanock, Timothy Eisen, Richard S. Houlston

Research output: Contribution to journalArticle

Abstract

Genome-wide association studies (GWASs) of renal cell cancer (RCC) have identified four susceptibility loci thus far. To identify an additional RCC common susceptibility locus, we conducted a GWAS and performed a meta-analysis with published GWASs (totalling 2215 cases and 8566 controls of European background) and followed up the most significant association signals [nine single nucleotide polymorphisms (SNPs) in eight genomic regions] in 3739 cases and 8786 controls. A combined analysis identified a novel susceptibility locus mapping to 2q22.3 marked by rs12105918 (P = 1.80 × 10-8; odds ratio 1.29, 95% CI: 1.18-1.41). The signal localizes to intron 2 of the ZEB2 gene (zinc finger E box-binding homeobox 2). Our findings suggest that genetic variation in ZEB2 influences the risk of RCC. This finding provides further insights into the genetic and biological basis of inherited genetic susceptibility to RCC.

Original languageEnglish (US)
Article numberdds489
Pages (from-to)825-831
Number of pages7
JournalHuman Molecular Genetics
Volume22
Issue number4
DOIs
StatePublished - Feb 2013
Externally publishedYes

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Kidney Neoplasms
Renal Cell Carcinoma
Genome-Wide Association Study
Homeobox Genes
Zinc Fingers
Genetic Predisposition to Disease
Introns
Single Nucleotide Polymorphism
Meta-Analysis
Odds Ratio
Genes

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)
  • Molecular Biology

Cite this

Henrion, M., Frampton, M., Scelo, G., Purdue, M., Ye, Y., Broderick, P., ... Houlston, R. S. (2013). Common variation at 2q22.3 (ZEB2) influences the risk of renal cancer. Human Molecular Genetics, 22(4), 825-831. [dds489]. https://doi.org/10.1093/hmg/dds489

Common variation at 2q22.3 (ZEB2) influences the risk of renal cancer. / Henrion, Marc; Frampton, Matthew; Scelo, Ghislaine; Purdue, Mark; Ye, Yuanqing; Broderick, Peter; Ritchie, Alastair; Kaplan, Richard; Meade, Angela; Mckay, James; Johansson, Mattias; Lathrop, Mark; Larkin, James; Rothman, Nathaniel; Wang, Zhaoming; Chow, Wong Ho; Stevens, Victoria L.; Ryan Diver, W.; Gapstur, Susan M.; Albanes, Demetrius; Virtamo, Jarmo; Wu, Xifeng; Brennan, Paul; Chanock, Stephen; Eisen, Timothy; Houlston, Richard S.

In: Human Molecular Genetics, Vol. 22, No. 4, dds489, 02.2013, p. 825-831.

Research output: Contribution to journalArticle

Henrion, M, Frampton, M, Scelo, G, Purdue, M, Ye, Y, Broderick, P, Ritchie, A, Kaplan, R, Meade, A, Mckay, J, Johansson, M, Lathrop, M, Larkin, J, Rothman, N, Wang, Z, Chow, WH, Stevens, VL, Ryan Diver, W, Gapstur, SM, Albanes, D, Virtamo, J, Wu, X, Brennan, P, Chanock, S, Eisen, T & Houlston, RS 2013, 'Common variation at 2q22.3 (ZEB2) influences the risk of renal cancer', Human Molecular Genetics, vol. 22, no. 4, dds489, pp. 825-831. https://doi.org/10.1093/hmg/dds489
Henrion M, Frampton M, Scelo G, Purdue M, Ye Y, Broderick P et al. Common variation at 2q22.3 (ZEB2) influences the risk of renal cancer. Human Molecular Genetics. 2013 Feb;22(4):825-831. dds489. https://doi.org/10.1093/hmg/dds489
Henrion, Marc ; Frampton, Matthew ; Scelo, Ghislaine ; Purdue, Mark ; Ye, Yuanqing ; Broderick, Peter ; Ritchie, Alastair ; Kaplan, Richard ; Meade, Angela ; Mckay, James ; Johansson, Mattias ; Lathrop, Mark ; Larkin, James ; Rothman, Nathaniel ; Wang, Zhaoming ; Chow, Wong Ho ; Stevens, Victoria L. ; Ryan Diver, W. ; Gapstur, Susan M. ; Albanes, Demetrius ; Virtamo, Jarmo ; Wu, Xifeng ; Brennan, Paul ; Chanock, Stephen ; Eisen, Timothy ; Houlston, Richard S. / Common variation at 2q22.3 (ZEB2) influences the risk of renal cancer. In: Human Molecular Genetics. 2013 ; Vol. 22, No. 4. pp. 825-831.
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