Robbins Christiane, Torres Jada Benn, Hooker Stanley, Bonilla Carolina, Hernandez Wenndy, Candreva Angela, Ahaghotu Chiledum, Kittles Rick, Carpten John
Division of Integrated Cancer Genomics, Translational Genomics Research Institute, Phoenix, Arizona 85004, USA.
Genome Res. 2007 Dec;17(12):1717-22. doi: 10.1101/gr.6782707. Epub 2007 Oct 31.
Prostate cancer is a common complex disease that disproportionately affects men of African descent. Recently, several different common variants on chromosome 8q24 have been shown to be associated with prostate cancer in multiple studies and ethnic groups. The objective of this study was to confirm the association of 8q24 markers with prostate cancer in African Americans. We genotyped 24 markers along 8q24 and 80 unlinked ancestry informative markers in a hospital-based case-control sample of 1057 African American men (490 prostate cancer cases and 567 controls). Association analyses of 8q24 markers with prostate cancer risk were adjusted for both global and local 8q24 admixture stratification using estimates from ancestry informative markers. We report that rs7008482, which maps to the 8q24.13 region, is an additional independent prostate cancer risk variant (P = 5 x 10(-4)), and we also replicate the association of rs16901979 with prostate cancer (P = 0.002). Other published risk variants in the region such as rs1447295 and rs6983267 showed a similar direction and magnitude of effect, but were not significant in our population. Both rs7008482 and rs16901979 independently predicted risk and remained significant (P < 0.001) after controlling for each other. Our data combined with additional replications of 8q24 markers provide compelling support for multiple regions of risk for prostate cancer on 8q24.
前列腺癌是一种常见的复杂疾病,对非洲裔男性的影响尤为严重。最近,多项研究和不同种族群体的研究表明,8号染色体q24区域的几种不同常见变异与前列腺癌有关。本研究的目的是在非裔美国人中证实8q24标记与前列腺癌的关联。我们对1057名非裔美国男性(490例前列腺癌病例和567例对照)的医院病例对照样本中的24个8q24标记和80个不连锁的祖先信息标记进行了基因分型。使用祖先信息标记的估计值,对8q24标记与前列腺癌风险的关联分析进行了全球和局部8q24混合分层调整。我们报告,定位于8q24.13区域的rs7008482是另一个独立的前列腺癌风险变异(P = 5 x 10(-4)),并且我们还重复了rs16901979与前列腺癌的关联(P = 0.002)。该区域其他已发表的风险变异,如rs1447295和rs6983267,显示出相似的效应方向和大小,但在我们的人群中不显著。rs7008482和rs16901979都独立预测风险,并且在相互控制后仍然显著(P < 0.001)。我们的数据与8q24标记的其他重复研究相结合,为8q24上前列腺癌的多个风险区域提供了有力支持。