Schadt Eric E, Lum Pek Y
Rosetta Inpharmatics, LLC, Seattle, WA 98109, USA.
J Lipid Res. 2006 Dec;47(12):2601-13. doi: 10.1194/jlr.R600026-JLR200. Epub 2006 Oct 1.
Diseases such as obesity, diabetes, and atherosclerosis result from multiple genetic and environmental factors, and importantly, interactions between genetic and environmental factors. Identifying susceptibility genes for these diseases using genetic and genomic technologies is accelerating, and the expectation over the next several years is that a number of genes will be identified for common diseases. However, the identification of single genes for disease has limited utility, given that diseases do not originate in complex systems from single gene changes. Further, the identification of single genes for disease may not lead directly to genes that can be targeted for therapeutic intervention. Therefore, uncovering single genes for disease in isolation of the broader network of molecular interactions in which they operate will generally limit the overall utility of such discoveries. Several integrative approaches have been developed and applied to reconstructing networks. Here we review several of these approaches that involve integrating genetic, expression, and clinical data to elucidate networks underlying disease. Networks reconstructed from these data provide a richer context in which to interpret associations between genes and disease. Therefore, these networks can lead to defining pathways underlying disease more objectively and to identifying biomarkers and more-robust points for therapeutic intervention.
肥胖、糖尿病和动脉粥样硬化等疾病是由多种遗传和环境因素,以及遗传和环境因素之间的相互作用导致的。利用遗传和基因组技术识别这些疾病的易感基因正在加速,预计在未来几年内将为常见疾病识别出一些基因。然而,鉴于疾病并非源于单一基因变化的复杂系统,识别单一疾病基因的作用有限。此外,识别单一疾病基因可能不会直接导向可用于治疗干预的靶点基因。因此,孤立地发现单一疾病基因而不考虑其所处的更广泛分子相互作用网络,通常会限制此类发现的整体效用。已经开发并应用了几种整合方法来重建网络。在此,我们综述其中几种涉及整合遗传、表达和临床数据以阐明疾病潜在网络的方法。从这些数据重建的网络提供了一个更丰富的背景,以便解释基因与疾病之间的关联。因此,这些网络能够更客观地定义疾病的潜在途径,并识别生物标志物以及更可靠的治疗干预靶点。