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Large-scale transcriptome-wide association study identifies new prostate cancer risk regions
by
Haiman, Christopher
, Pasaniuc, Bogdan
, Zheng, Wei
, Penney, Kathryn L.
, Freedman, Matthew
, Kote-Jarai, Zsofia
, Eeles, Rosalind
, Mancuso, Nicholas
, Gayther, Simon
, Gusev, Alexander
in
38/43
/ 631/208/199
/ 631/208/205/2138
/ 631/208/68
/ Alternative splicing
/ Bayesian analysis
/ Gene expression
/ Genes
/ Genome-wide association studies
/ Genome-Wide Association Study
/ Genomes
/ Health risks
/ Humanities and Social Sciences
/ Humans
/ Loci
/ Male
/ Mathematical models
/ multidisciplinary
/ Prostate cancer
/ Prostatic Neoplasms - genetics
/ Prostatic Neoplasms - metabolism
/ Risk
/ Science
/ Science (multidisciplinary)
/ Single-nucleotide polymorphism
/ Splicing
/ Transcriptome
/ Tumorigenesis
/ Tumors
2018
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Large-scale transcriptome-wide association study identifies new prostate cancer risk regions
by
Haiman, Christopher
, Pasaniuc, Bogdan
, Zheng, Wei
, Penney, Kathryn L.
, Freedman, Matthew
, Kote-Jarai, Zsofia
, Eeles, Rosalind
, Mancuso, Nicholas
, Gayther, Simon
, Gusev, Alexander
in
38/43
/ 631/208/199
/ 631/208/205/2138
/ 631/208/68
/ Alternative splicing
/ Bayesian analysis
/ Gene expression
/ Genes
/ Genome-wide association studies
/ Genome-Wide Association Study
/ Genomes
/ Health risks
/ Humanities and Social Sciences
/ Humans
/ Loci
/ Male
/ Mathematical models
/ multidisciplinary
/ Prostate cancer
/ Prostatic Neoplasms - genetics
/ Prostatic Neoplasms - metabolism
/ Risk
/ Science
/ Science (multidisciplinary)
/ Single-nucleotide polymorphism
/ Splicing
/ Transcriptome
/ Tumorigenesis
/ Tumors
2018
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Large-scale transcriptome-wide association study identifies new prostate cancer risk regions
by
Haiman, Christopher
, Pasaniuc, Bogdan
, Zheng, Wei
, Penney, Kathryn L.
, Freedman, Matthew
, Kote-Jarai, Zsofia
, Eeles, Rosalind
, Mancuso, Nicholas
, Gayther, Simon
, Gusev, Alexander
in
38/43
/ 631/208/199
/ 631/208/205/2138
/ 631/208/68
/ Alternative splicing
/ Bayesian analysis
/ Gene expression
/ Genes
/ Genome-wide association studies
/ Genome-Wide Association Study
/ Genomes
/ Health risks
/ Humanities and Social Sciences
/ Humans
/ Loci
/ Male
/ Mathematical models
/ multidisciplinary
/ Prostate cancer
/ Prostatic Neoplasms - genetics
/ Prostatic Neoplasms - metabolism
/ Risk
/ Science
/ Science (multidisciplinary)
/ Single-nucleotide polymorphism
/ Splicing
/ Transcriptome
/ Tumorigenesis
/ Tumors
2018
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Large-scale transcriptome-wide association study identifies new prostate cancer risk regions
Journal Article
Large-scale transcriptome-wide association study identifies new prostate cancer risk regions
2018
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Overview
Although genome-wide association studies (GWAS) for prostate cancer (PrCa) have identified more than 100 risk regions, most of the risk genes at these regions remain largely unknown. Here we integrate the largest PrCa GWAS (
N
= 142,392) with gene expression measured in 45 tissues (
N
= 4458), including normal and tumor prostate, to perform a multi-tissue transcriptome-wide association study (TWAS) for PrCa. We identify 217 genes at 84 independent 1 Mb regions associated with PrCa risk, 9 of which are regions with no genome-wide significant SNP within 2 Mb. 23 genes are significant in TWAS only for alternative splicing models in prostate tumor thus supporting the hypothesis of splicing driving risk for continued oncogenesis. Finally, we use a Bayesian probabilistic approach to estimate credible sets of genes containing the causal gene at a pre-defined level; this reduced the list of 217 associations to 109 genes in the 90% credible set. Overall, our findings highlight the power of integrating expression with PrCa GWAS to identify novel risk loci and prioritize putative causal genes at known risk loci.
Genome-wide association studies (GWAS) have identified hundreds of genomic risk regions for prostate cancer. Here, the authors perform a transcriptome wide association study (TWAS) by incorporating prostate cancer GWAS with gene expression data to identify potential novel prostate cancer risk loci and possible risk mechanisms.
Publisher
Nature Publishing Group UK,Nature Publishing Group,Nature Portfolio
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