| Literature DB >> 21274727 |
Christopher J Ward1, Yanhong Wu, Ruth A Johnson, John R Woollard, Eric J Bergstralh, Mine S Cicek, Jason Bakeberg, Sandro Rossetti, Christina M Heyer, Gloria M Petersen, Noralene M Lindor, Stephen N Thibodeau, Peter C Harris, Vicente E Torres, Marie C Hogan, Lisa A Boardman.
Abstract
The autosomal recessive polycystic kidney disease (ARPKD) gene, PKHD1, has been implicated in the genesis or growth of colorectal adenocarcinoma, as a high level of somatic mutations was found in colorectal tumor tissue. To determine whether carriers of a single PKHD1 mutation are at increased risk of colorectal carcinoma, we assessed the prevalence of the commonest European mutation, T36M. First, we assayed a European cohort of ARPKD patients and found T36M was responsible for 13.1% of mutations. We then investigated two European cohorts with colorectal adenocarcinoma versus two control cohorts of similar age and gender. Screening for the most common PKHD1 mutation, T36M, we detected 15:3,603 (0.42%) controls versus 1:3,767 (0.027%) colorectal cancer individuals, indicating that heterozygous PKHD1 mutations are not a risk factor and are protective (p=0.0002). We also show that the carriage rate for PKHD1 mutations in the European population is higher than previous accepted at 3.2% (1:31 genomes). © Springer-Verlag 2010Entities:
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Year: 2011 PMID: 21274727 PMCID: PMC3102497 DOI: 10.1007/s00439-011-0950-8
Source DB: PubMed Journal: Hum Genet ISSN: 0340-6717 Impact factor: 4.132