Yeager Meredith, Xiao Nianqing, Hayes Richard B, Bouffard Pascal, Desany Brian, Burdett Laura, Orr Nick, Matthews Casey, Qi Liqun, Crenshaw Andrew, Markovic Zdenek, Fredrikson Karin M, Jacobs Kevin B, Amundadottir Laufey, Jarvie Thomas P, Hunter David J, Hoover Robert, Thomas Gilles, Harkins Timothy T, Chanock Stephen J
Core Genotyping Facility, Advanced Technology Program, SAIC-Frederick, Inc., NCI-Frederick, Frederick, MD 21702, USA.
Hum Genet. 2008 Sep;124(2):161-70. doi: 10.1007/s00439-008-0535-3. Epub 2008 Aug 14.
Recently, genome-wide association studies have identified loci across a segment of chromosome 8q24 (128,100,000-128,700,000) associated with the risk of breast, colon and prostate cancers. At least three regions of 8q24 have been independently associated with prostate cancer risk; the most centromeric of which appears to be population specific. Haplotypes in two contiguous but independent loci, marked by rs6983267 and rs1447295, have been identified in the Cancer Genetic Markers of Susceptibility project ( http://cgems.cancer.gov ), which genotyped more than 5,000 prostate cancer cases and 5,000 controls of European origin. The rs6983267 locus is also strongly associated with colorectal cancer. To ascertain a comprehensive catalog of common single-nucleotide polymorphisms (SNPs) across the two regions, we conducted a resequence analysis of 136 kb (chr8: 128,473,000-128,609,802) using the Roche/454 next-generation sequencing technology in 39 prostate cancer cases and 40 controls of European origin. We have characterized a comprehensive catalog of common (MAF > 1%) SNPs within this region, including 442 novel SNPs and have determined the pattern of linkage disequilibrium across the region. Our study has generated a detailed map of genetic variation across the region, which should be useful for choosing SNPs for fine mapping of association signals in 8q24 and investigations of the functional consequences of select common variants.
最近,全基因组关联研究已经确定了8号染色体8q24区段(128,100,000 - 128,700,000)上的一些基因座,这些基因座与乳腺癌、结肠癌和前列腺癌的风险相关。8q24至少有三个区域已被独立证明与前列腺癌风险相关;其中最靠近着丝粒的区域似乎具有人群特异性。在癌症遗传易感性标记项目(http://cgems.cancer.gov)中,已经在两个相邻但独立的基因座中鉴定出了以rs6983267和rs1447295为标记的单倍型,该项目对5000多例欧洲裔前列腺癌病例和5000例对照进行了基因分型。rs6983267基因座也与结直肠癌密切相关。为了确定这两个区域常见单核苷酸多态性(SNP)的完整目录,我们使用罗氏/454下一代测序技术,对39例欧洲裔前列腺癌病例和40例对照进行了136 kb(chr8: 128,473,000 - 128,609,802)的重测序分析。我们已经对该区域内常见(MAF > 1%)SNP的完整目录进行了特征描述,包括442个新的SNP,并确定了整个区域的连锁不平衡模式。我们的研究绘制了该区域详细的遗传变异图谱,这对于选择SNP对8q24的关联信号进行精细定位以及研究特定常见变异的功能后果应该是有用的。