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Mining heterogeneous network for drug repositioning using phenotypic information extracted from social media and pharmaceutical databases

机译:使用从社交媒体和药物数据库中提取的表型信息来挖掘用于药物重新定位的异构网络

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Drug repositioning has drawn significant attention for drug development in pharmaceutical research and industry, because of its advantages in cost and time compared with the de novo drug development. The availability of biomedical databases and online health-related information, as well as the high-performance computing, empowers the development of computational drug repositioning methods. In this work, we developed a systematic approach that identifies repositioning drugs based on heterogeneous network mining using both pharmaceutical databases (PharmGKB and SIDER) and online health community (MedHelp). By utilizing adverse drug reactions (ADRs) as the intermediate, we constructed a heterogeneous health network containing drugs, diseases, and ADRs, and developed path-based heterogeneous network mining approaches for drug repositioning. Additionally, we investigated on how the data sources affect the performance on drug repositioning. Experiment results showed that combining both PharmKGB and MedHelp identified 479 repositioning drugs, which are more than the repositioning drugs discovered by other alternatives. In addition, 31% of the 479 of the discovered repositioning drugs were supported by evidence from PubMed.
机译:与从头开发药物相比,药物重新定位因其在成本和时间上的优势而在药物研究和工业领域引起了极大的关注。生物医学数据库和在线健康相关信息的可用性以及高性能计算功能,使计算药物重新定位方法的开发成为可能。在这项工作中,我们开发了一种系统的方法,该方法使用药物数据库(PharmGKB和SIDER)和在线健康社区(MedHelp)基于异类网络挖掘来识别重新定位药物。通过利用药物不良反应(ADR)作为中间体,我们构建了包含药物,疾病和ADR的异构健康网络,并开发了基于路径的异构网络挖掘方法来进行药物重新定位。此外,我们调查了数据源如何影响药物重新定位的性能。实验结果表明,结合使用PharmKGB和MedHelp可以识别479种重定位药物,这比其他替代品发现的重定位药物要多。此外,在479种发现的重新定位药物中,有31%得到PubMed的证据支持。

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