Comprehensive Resequence Analysis of a 97 kb Region of Chromosome 10q11.2 Containing the MSMB Gene Associated with Prostate Cancer

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Comprehensive Resequence Analysis of a 97 kb Region of Chromosome 10q11.2 Containing the MSMB Gene Associated with Prostate Cancer

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Title: Comprehensive Resequence Analysis of a 97 kb Region of Chromosome 10q11.2 Containing the MSMB Gene Associated with Prostate Cancer
Author: Yeager, Meredith; Deng, Zuoming; Boland, Joseph; Matthews, Casey; Bacior, Jennifer; Lonsberry, Victor; Hutchinson, Amy; Burdett, Laura A.; Qi, Liqun; Jacobs, Kevin B.; Gonzalez-Bosquet, Jesus; Berndt, Sonja I.; Hayes, Richard B.; Hoover, Robert N.; Thomas, Gilles; Dean, Michael; Chanock, Stephen J.; Hunter, David J.

Note: Order does not necessarily reflect citation order of authors.

Citation: Yeager, Meredith, Zuoming Deng, Joseph Boland, Casey Matthews, Jennifer Bacior, Victor Lonsberry, Amy Hutchinson, et al. 2009. Comprehensive resequence analysis of a 97 kb region of chromosome 10q11.2 containing the gene associated with prostate cancer. Human Genetics 126(6): 743-750.
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Abstract: Genome-wide association studies of prostate cancer have identified single nucleotide polymorphism (SNP) markers in a region of chromosome 10q11.2, harboring the microseminoprotein-β (MSMB) gene. Both the gene product of MSMB, the prostate secretory protein 94 (PSP94) and its binding protein (PSPBP), have been previously investigated as serum biomarkers for prostate cancer progression. Recent functional work has shown that different alleles of the significantly associated SNP in the promoter of MSMB found to be associated with prostate cancer risk, rs10993994, can influence its expression in tumors and in vitro studies. Since it is plausible that additional variants in this region contribute to the risk of prostate cancer, we have used next-generation sequencing technology to resequence a ~97-kb region that includes the area surrounding MSMB (chr10: 51,168,025–51,265,101) in 36 prostate cancer cases, 26 controls of European origin, and 8 unrelated CEPH individuals in order to identify additional variants to investigate in functional studies. We identified 241 novel polymorphisms within this region, including 142 in the 51-kb block of linkage disequilibrium (LD) that contains rs10993994 and the proximal promoter of MSMB. No sites were observed to be polymorphic within the exons of MSMB. Electronic supplementary material: The online version of this article (doi:10.1007/s00439-009-0723-9) contains supplementary material, which is available to authorized users.
Published Version: doi://10.1007/s00439-009-0723-9
Other Sources: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2778717/pdf/
Terms of Use: This article is made available under the terms and conditions applicable to Other Posted Material, as set forth at http://nrs.harvard.edu/urn-3:HUL.InstRepos:dash.current.terms-of-use#LAA
Citable link to this page: http://nrs.harvard.edu/urn-3:HUL.InstRepos:4791065

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