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Predicting Pharmacodynamic Drug-Drug Interactions through Signaling Propagation Interference on Protein-Protein Interaction Networks

机译:通过信号在蛋白质-蛋白质相互作用网络上的传播干扰来预测药效学药物-药物相互作用

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摘要

As pharmacodynamic drug-drug interactions (PD DDIs) could lead to severe adverse effects in patients, it is important to identify potential PD DDIs in drug development. The signaling starting from drug targets is propagated through protein-protein interaction (PPI) networks. PD DDIs could occur by close interference on the same targets or within the same pathways as well as distant interference through cross-talking pathways. However, most of the previous approaches have considered only close interference by measuring distances between drug targets or comparing target neighbors. We have applied a random walk with restart algorithm to simulate signaling propagation from drug targets in order to capture the possibility of their distant interference. Cross validation with DrugBank and Kyoto Encyclopedia of Genes and Genomes DRUG shows that the proposed method outperforms the previous methods significantly. We also provide a web service with which PD DDIs for drug pairs can be analyzed at .
机译:由于药效动力学的药物-药物相互作用(PD DDI)可能导致严重的患者不良反应,因此在药物开发中确定潜在的PD DDI很重要。从药物靶标开始的信号传导通过蛋白质-蛋白质相互作用(PPI)网络传播。 PD DDI可能通过对相同目标或相同路径内的紧密干扰以及通过串扰路径的远距离干扰而发生。但是,大多数先前的方法仅通过测量药物靶标之间的距离或比较靶标邻居之间的距离来考虑仅存在紧密干扰。我们已经应用了带有重新启动算法的随机行走,以模拟来自药物靶标的信号传播,以便捕获其远距离干扰的可能性。与DrugBank和《京都市基因与基因组百科全书》的交叉验证表明,该方法明显优于以前的方法。我们还提供了一项Web服务,可在处分析药物对的PD DDI。

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