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A Systematic Framework for Drug Repositioning from Integrated Omics and Drug Phenotype Profiles Using Pathway-Drug Network

机译:使用途径 - 药物网络从集成常常和药物表型分布中排入的系统框架

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摘要

Drug repositioning offers new clinical indications for old drugs. Recently, many computational approaches have been developed to repurpose marketed drugs in human diseases by mining various of biological data including disease expression profiles, pathways, drug phenotype expression profiles, and chemical structure data. However, despite encouraging results, a comprehensive and efficient computational drug repositioning approach is needed that includes the high-level integration of available resources. In this study, we propose a systematic framework employing experimental genomic knowledge and pharmaceutical knowledge to reposition drugs for a specific disease. Specifically, we first obtain experimental genomic knowledge from disease gene expression profiles and pharmaceutical knowledge from drug phenotype expression profiles and construct a pathway-drug network representing a priori known associations between drugs and pathways. To discover promising candidates for drug repositioning, we initialize node labels for the pathway-drug network using identified disease pathways and known drugs associated with the phenotype of interest and perform network propagation in a semisupervised manner. To evaluate our method, we conducted some experiments to reposition 1309 drugs based on four different breast cancer datasets and verified the results of promising candidate drugs for breast cancer by a two-step validation procedure. Consequently, our experimental results showed that the proposed framework is quite useful approach to discover promising candidates for breast cancer treatment.
机译:药物重新定位为旧药物提供新的临床适应症。最近,已经开发了许多计算方法来通过挖掘各种生物数据,包括疾病表达谱,途径,药物表型表达曲线和化学结构数据,以通过挖掘各种生物数据来对人类疾病中的销售药物进行复发。但是,尽管令人鼓舞的结果,需要全面高效的计算药物重新定位方法,包括可用资源的高级集成。在这项研究中,我们提出了一种系统框架,采用实验基因组知识和药物知识来重新定位特定疾病的药物。具体地,我们首先从药物表型表达谱中获得来自疾病基因表达谱和药物知识的实验基因组知识,并构建代表药物和途径之间的先知相关联的途径 - 药物网络。为了发现有希望的药物重新定位候选者,我们使用与感兴趣的表型相关的鉴定的疾病途径和已知药物初始化途径 - 药物网络的节点标签,并以半熟的方式进行网络传播。为了评估我们的方法,我们进行了一些基于四种不同的乳腺癌数据集重新定位1309药物的实验,并通过两步验证程序验证了对乳腺癌的有前途候选药物的结果。因此,我们的实验结果表明,拟议的框架是探索乳腺癌治疗有希望候选人的相当实用的方法。

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