Abstract
Prostate cancer is the most frequently diagnosed cancer in males in developed countries. To identify common prostate cancer susceptibility alleles, we genotyped 211,155 SNPs on a custom Illumina array (iCOGS) in blood DNA from 25,074 prostate cancer cases and 24,272 controls from the international PRACTICAL Consortium. Twenty-three new prostate cancer susceptibility loci were identified at genome-wide significance (P<5×10(-8)). More than 70 prostate cancer susceptibility loci, explaining ~30% of the familial risk for this disease, have now been identified. On the basis of combined risks conferred by the new and previously known risk loci, the top 1% of the risk distribution has a 4.7-fold higher risk than the average of the population being profiled. These results will facilitate population risk stratification for clinical studies.
| Original language | English |
|---|---|
| Journal | Urologic Oncology |
| Volume | 32 |
| Issue number | 2 |
| Pages (from-to) | 211 |
| ISSN | 1078-1439 |
| DOIs | |
| Publication status | Published - Feb 2014 |
Keywords
- Genetic Loci
- Genetic Predisposition to Disease
- Humans
- Male
- Polymorphism, Single Nucleotide
- Prostatic Neoplasms
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Dive into the research topics of 'Commentary on "identification of 23 new prostate cancer susceptibility loci using the iCOGS custom genotyping array." COGS-Cancer Research UK GWAS-ELLIPSE (part of GAME-ON) Initiative; Australian Prostate Cancer Bioresource; UK Genetic Prostate Cancer Study Collaborators/British Association of Urological Surgeons' Section of Oncology; UK ProtecT (Prostate testing for cancer and Treatment) Study'. Together they form a unique fingerprint.Cite this
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