| Literature DB >> 24974847 |
Laura Fachal1, Antonio Gómez-Caamaño2, Gillian C Barnett3, Paula Peleteiro2, Ana M Carballo2, Patricia Calvo-Crespo2, Sarah L Kerns4, Manuel Sánchez-García5, Ramón Lobato-Busto5, Leila Dorling3, Rebecca M Elliott6, David P Dearnaley7, Matthew R Sydes8, Emma Hall9, Neil G Burnet10, Ángel Carracedo11, Barry S Rosenstein4, Catharine M L West6, Alison M Dunning3, Ana Vega1.
Abstract
There is increasing evidence supporting the role of genetic variants in the development of radiation-induced toxicity. However, previous candidate gene association studies failed to elucidate the common genetic variation underlying this phenotype, which could emerge years after the completion of treatment. We performed a genome-wide association study on a Spanish cohort of 741 individuals with prostate cancer treated with external beam radiotherapy (EBRT). The replication cohorts consisted of 633 cases from the UK and 368 cases from North America. One locus comprising TANC1 (lowest unadjusted P value for overall late toxicity=6.85×10(-9), odds ratio (OR)=6.61, 95% confidence interval (CI)=2.23-19.63) was replicated in the second stage (lowest unadjusted P value for overall late toxicity=2.08×10(-4), OR=6.17, 95% CI=2.25-16.95; Pcombined=4.16×10(-10)). The inclusion of the third cohort gave unadjusted Pcombined=4.64×10(-11). These results, together with the role of TANC1 in regenerating damaged muscle, suggest that the TANC1 locus influences the development of late radiation-induced damage.Entities:
Mesh:
Year: 2014 PMID: 24974847 DOI: 10.1038/ng.3020
Source DB: PubMed Journal: Nat Genet ISSN: 1061-4036 Impact factor: 38.330