Comprehensive Resequence Analysis of a 97 kb Region of Chromosome 10q11.2 Containing the MSMB Gene Associated with Prostate Cancer
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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.
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https://doi.org/10.1007/s00439-009-0723-9Metadata
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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.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.Other Sources
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2778717/pdf/Terms of Use
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