Department of Preventive Medicine, Keck School of Medicine, University of Southern California, Norris Comprehensive Cancer Center, Los Angeles, California, USA.
Nat Genet. 2011 Jun;43(6):570-3. doi: 10.1038/ng.839. Epub 2011 May 22.
In search of common risk alleles for prostate cancer that could contribute to high rates of the disease in men of African ancestry, we conducted a genome-wide association study, with 1,047,986 SNP markers examined in 3,425 African-Americans with prostate cancer (cases) and 3,290 African-American male controls. We followed up the most significant 17 new associations from stage 1 in 1,844 cases and 3,269 controls of African ancestry. We identified a new risk variant on chromosome 17q21 (rs7210100, odds ratio per allele = 1.51, P = 3.4 × 10(-13)). The frequency of the risk allele is ∼5% in men of African descent, whereas it is rare in other populations (<1%). Further studies are needed to investigate the biological contribution of this allele to prostate cancer risk. These findings emphasize the importance of conducting genome-wide association studies in diverse populations.
为了寻找可能导致非洲裔男性前列腺癌发病率较高的常见风险等位基因,我们进行了一项全基因组关联研究,在 3425 名患有前列腺癌的非洲裔美国人(病例)和 3290 名非洲裔美国男性对照中检查了 1047986 个 SNP 标记。我们在 1844 名非洲裔病例和 3269 名对照中对第一阶段发现的 17 个最显著的新关联进行了随访。我们在 17q21 染色体上发现了一个新的风险变异体(rs7210100,每个等位基因的优势比=1.51,P=3.4×10(-13))。风险等位基因在非洲裔男性中的频率约为 5%,而在其他人群中则很少(<1%)。需要进一步的研究来探讨该等位基因对前列腺癌风险的生物学贡献。这些发现强调了在不同人群中进行全基因组关联研究的重要性。