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ARLTS1 germline variants and the risk for breast, prostate, and colorectal cancer
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2008 (English)In: European Journal of Human Genetics, ISSN 1018-4813, Vol. 16, no 8, 983-91 p.Article in journal (Refereed) Published
Abstract [en]

Recently, a nonsense alteration Trp149Stop in the ARLTS1 gene was found more frequently in familial cancer cases versus sporadic cancer patients and healthy controls. Here, the role of Trp149Stop or any other ARLTS1 germline variant was evaluated on breast, prostate, and colorectal cancer risk. The whole gene was screened for germline alterations in 855 familial cancer patients. The five observed variants were further screened in 1169 non-familial cancer patients as well as in 809 healthy population controls. The Trp149Stop was found at low frequencies (0.5-1.2%) in all patient subgroups versus 1.6% in controls, and the mutant allele did not co-segregate with disease status in families with multiple affected individuals. The CC genotype in the Cys148Arg variant was slightly more common among both familial and sporadic breast (odds ratio (OR), 1.48; 95% confidence interval (CI), 1.16-1.87; P=0.001) and prostate cancer patients (OR, 1.50; 95% CI, 1.13-1.99; P=0.005) when compared to controls. A novel ARLTS1 variant Gly65Val was found at higher frequency among familial prostate cancer patients (8 of 164, 4.9%) than in controls (13 of 809, 1.6%; OR, 3.14; 95% CI, 1.28-7.70, P=0.016). However, after adjusting for multiple testing, none of these results were still significant. No association was found with any of the variants and colorectal cancer risk. Our results suggest that Trp149Stop is not a predisposition allele in breast, prostate, or colorectal cancer in the Finnish population, and, while the Gly65Val variant may increase familial prostate cancer risk and the Cys148Arg change may affect both breast and prostate cancer risk, the evidence is not strong in these data.

Place, publisher, year, edition, pages
2008. Vol. 16, no 8, 983-91 p.
National Category
Medical and Health Sciences
URN: urn:nbn:se:uu:diva-105399DOI: 10.1038/ejhg.2008.43PubMedID: 18337727OAI: oai:DiVA.org:uu-105399DiVA: diva2:221177
Available from: 2009-06-03 Created: 2009-06-03 Last updated: 2009-06-08Bibliographically approved

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