Journal article
Dependence of colorectal cancer risk on the parent-of-origin of mutations in DNA mismatch repair genes
CM Van Vliet, JG Dowty, JL Van Vliet, L Smith, LJ Mead, FA Macrae, DJB St. John, GG Giles, MC Southey, MA Jenkins, GM Velan, JL Hopper
Human Mutation | WILEY | Published : 2011
DOI: 10.1002/humu.21408
Abstract
Genetic diseases associated with dynamic mutations in microsatellite DNA often display parent-of-origin effects (POEs) in which the risk of disease depends on the sex of the parent from whom the disease allele was inherited. Carriers of germline mutations in mismatch repair (MMR) genes have high risks of colorectal carcinoma (CRC). We investigated whether these risks depend on the parent-of-origin of the mutation. We studied 422 subjects, including 89 MMR gene mutation carriers, from 17 population-based families who were each recruited via a CRC case diagnosed before age 45 years and found to carry a MMR gene mutation. The POE hazard ratio (HRPOE), defined to be the CRC incidence for carrier..
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Awarded by National Cancer Institute
Funding Acknowledgements
Contract grant sponsors: Australian Postgraduate Award from the Australian Research Council; NHMRC. We thank the participants in the Victorian Colorectal Cancer Family Study, which has been funded by the Victorian Health Promotion Foundation and the Australian National Health and Medical Research Council (NHMRC). M.C.S. is a Senior Research Fellow of the NHMRC and J.L.H. is a NHMRC Australia Fellow.