首页> 外文期刊>Journal of Lipid Research >Thematic review series: systems biology approaches to metabolic and cardiovascular disorders. Reverse engineering gene networks to identify key drivers of complex disease phenotypes.
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Thematic review series: systems biology approaches to metabolic and cardiovascular disorders. Reverse engineering gene networks to identify key drivers of complex disease phenotypes.

机译:专题回顾系列:代谢和心血管疾病的系统生物学方法。逆向工程基因网络,以识别复杂疾病表型的关键驱动因素。

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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.
机译: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引起的,而重要的是遗传和环境因素之间的相互作用。使用遗传和基因组技术来鉴定这些疾病的易感基因正在加速发展,并且在接下来的几年中,人们期望可以鉴定出许多常见疾病的基因。但是,鉴于疾病并非起源于单个基因变化的复杂系统,因此鉴定疾病的单个基因的用途有限。此外,疾病单一基因的鉴定可能不会直接导致可以作为治疗干预目标的基因。因此,孤立地发现疾病的单个基因来隔离它们在其中运作的更广泛的分子相互作用网络将通常限制这种发现的整体效用。已经开发了几种集成方法并将其应用于重构网络。在这里,我们回顾了其中涉及整合遗传,表达和临床数据以阐明潜在疾病网络的几种方法。从这些数据重建的网络提供了更丰富的背景,可用来解释基因与疾病之间的关联。因此,这些网络可以导致更客观地确定疾病的潜在途径,并确定用于治疗干预的生物标志物和更稳健的点。

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