Hicks Chindo, Asfour Rozana, Pannuti Antonio, Miele Lucio
Cancer Institute, University of Mississippi Medical Center, 2500 N. State Street, Jackson, MS, USA.
Cancer Inform. 2011;10:185-204. doi: 10.4137/CIN.S6837. Epub 2011 Jul 25.
Genome-wide association studies (GWAS) have successfully identified genetic variants associated with risk for breast cancer. However, the molecular mechanisms through which the identified variants confer risk or influence phenotypic expression remains poorly understood. Here, we present a novel integrative genomics approach that combines GWAS information with gene expression data to assess the combined contribution of multiple genetic variants acting within genes and putative biological pathways, and to identify novel genes and biological pathways that could not be identified using traditional GWAS. The results show that genes containing SNPs associated with risk for breast cancer are functionally related and interact with each other in biological pathways relevant to breast cancer. Additionally, we identified novel genes that are co-expressed and interact with genes containing SNPs associated with breast cancer. Integrative analysis combining GWAS information with gene expression data provides functional bridges between GWAS findings and biological pathways involved in breast cancer.
全基因组关联研究(GWAS)已成功鉴定出与乳腺癌风险相关的基因变异。然而,已鉴定出的变异赋予风险或影响表型表达的分子机制仍知之甚少。在此,我们提出了一种新颖的整合基因组学方法,该方法将GWAS信息与基因表达数据相结合,以评估多个基因变异在基因和假定生物途径中发挥作用的综合贡献,并识别使用传统GWAS无法鉴定的新基因和生物途径。结果表明,含有与乳腺癌风险相关单核苷酸多态性(SNP)的基因在功能上相关,并在与乳腺癌相关的生物途径中相互作用。此外,我们鉴定出了与含有乳腺癌相关SNP的基因共表达并相互作用的新基因。将GWAS信息与基因表达数据相结合的整合分析在GWAS发现与乳腺癌相关生物途径之间提供了功能桥梁。