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Network-Based Assessment of Adverse Drug Reaction Risk in Polypharmacy Using High-Throughput Screening Data

机译:使用高通量筛选数据的基于网络的多元药店药品不良反应风险评估

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摘要

The risk of adverse drug reactions increases in a polypharmacology setting. High-throughput drug screening with transcriptomics applied to human cells has shown that drugs have effects on several molecular pathways, and these affected pathways may be predictive proxy for adverse drug reactions. Depending on the way that different drugs may contribute to adverse drug reactions, different options may exist in the clinical setting. Here, we formulate a network framework to integrate the relationships between drugs, biological functions, and adverse drug reactions based on the high-throughput drug perturbation data from the Library of Integrated Network-Based Cellular Signatures (LINCS) project. We present network-based parameters that indicate whether a given reaction may be related to the effect of a single drug or to the combination of several drugs, as well as the relative risk of adverse drug reaction manifestation given a certain drug combination.
机译:在多药理学背景下,药物不良反应的风险增加。将转录组学应用于人细胞的高通量药物筛选显示,药物对几种分子途径有影响,而这些受影响的途径可能是药物不良反应的预测指标。根据不同药物可能导致药物不良反应的方式,临床环境中可能存在不同的选择。在这里,我们基于基于网络的集成细胞签名库(LINCS)项目中的高通量药物扰动数据,制定了一个网络框架来整合药物,生物学功能和药物不良反应之间的关系。我们提供基于网络的参数,这些参数指示给定的反应是否可能与单一药物的作用或几种药物的组合有关,以及给定某种药物组合时药物不良反应表现的相对风险。

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