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

机译:使用通路-药物网络从整合的组学和药物表型谱中重新定位药物的系统框架

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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了新的临床适应症。近来,已经开发了许多计算方法,以通过挖掘各种生物数据来重用市售药物用于人类疾病,这些生物数据包括疾病表达谱,途径,药物表型表达谱和化学结构数据。然而,尽管取得了令人鼓舞的结果,但仍需要一种全面有效的药物重新定位方法,其中包括对可用资源的高级集成。在这项研究中,我们提出了一个系统框架,利用实验性基因组知识和药物知识来为特定疾病重新定位药物。具体而言,我们首先从疾病基因表达谱获得实验基因组学知识,并从药物表型表达谱获得药物学知识,然后构建代表药物与途径之间先验已知关联的途径-药物网络。为了发现有希望的药物重新定位候选人,我们使用已确定的疾病途径和与目标表型相关的已知药物来初始化途径-药物网络的节点标签,并以半监督方式进行网络传播。为了评估我们的方法,我们进行了一些实验,以基于四个不同的乳腺癌数据集来重新定位1309种药物,并通过两步验证程序验证了有希望的乳腺癌候选药物的结果。因此,我们的实验结果表明,提出的框架对于发现有希望的乳腺癌治疗候选者是非常有用的方法。

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