首页> 外文OA文献 >Thematic review series: Systems Biology Approaches to Metabolic and Cardiovascular Disorders. Reverse engineering gene networks to identify key drivers of complex disease phenotypes
【2h】

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:专题审查系列:系统生物学对代谢和心血管障碍的方法。逆向工程基因网络识别复杂疾病表型的关键驱动因素

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

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来自多种遗传和环境因素,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鉴定这些疾病的易感性基因正在加速,并且接下来几年的期望是,将鉴定许多基因以普遍疾病。然而,鉴定单一的疾病基因具有有限的效用,鉴于疾病不源于单一基因变化的复杂系统。此外,鉴定单个疾病的鉴定可能不会直接导致可针对治疗干预的基因。因此,揭示单一基因的疾病,分离他们操作的分子相互作用的更广泛网络通常限制此类发现的整体效用。已经开发了几种综合方法并应用于重建网络。在这里,我们审查了涉及整合遗传,表达和临床数据的这些方法中的几种方法,以阐明疾病的网络。从这些数据重建的网络提供了一种更丰富的上下文,在其中解释基因和疾病之间的关联。因此,这些网络可以更客观地使途径疾病更加客观地和识别用于治疗干预的生物标志物和更强大的点。

著录项

  • 作者

    Eric E. Schadt; Pek Y. Lum;

  • 作者单位
  • 年度 2006
  • 总页数
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号