Institute for Human Genetics, Department of Epidemiology & Biostatistics, University of California, San Francisco, San Francisco, California, USA.
OMICS. 2011 Jun;15(6):393-8. doi: 10.1089/omi.2010.0090. Epub 2011 Feb 24.
Genome-wide association studies (GWAS) have successfully detected and replicated associations with numerous diseases, including cancers of the prostate and breast. These findings are helping clarify the genomic basis of such diseases, but appear to explain little of disease heritability. This limitation might reflect the focus of conventional GWAS on a small set of the most statistically significant associations with disease. More information might be obtained by analyzing GWAS using a polygenic model, which allows for the possibility that thousands of genetic variants could impact disease. Furthermore, there may exist common polygenic effects between potentially related phenotypes (e.g., prostate and breast cancer). Here we present and apply a polygenic model to GWAS of prostate and breast cancer. Our results indicate that the polygenic model can explain an increasing--albeit low--amount of heritability for both of these cancers, even when excluding the most statistically significant associations. In addition, nonaggressive prostate cancer and breast cancer appear to share a common polygenic model, potentially reflecting a similar underlying biology. This supports the further development and application of polygenic models to genomic data.
全基因组关联研究 (GWAS) 已成功检测到并复制了与许多疾病的关联,包括前列腺癌和乳腺癌。这些发现有助于阐明这些疾病的基因组基础,但似乎解释不了疾病遗传率的多少。这种局限性可能反映了传统 GWAS 对与疾病关联最显著的一小部分的关注。通过使用多基因模型分析 GWAS 可能会获得更多信息,因为这种模型允许数千种遗传变异可能会影响疾病的可能性。此外,在潜在相关表型(例如,前列腺癌和乳腺癌)之间可能存在共同的多基因效应。在这里,我们提出并应用了一种多基因模型来分析前列腺癌和乳腺癌的 GWAS。我们的研究结果表明,即使排除了最显著的关联,多基因模型也可以解释这两种癌症越来越多的遗传率,尽管这种遗传率很低。此外,侵袭性较低的前列腺癌和乳腺癌似乎共享一个共同的多基因模型,这可能反映了类似的潜在生物学。这支持了进一步开发和应用多基因模型来分析基因组数据。