B. Ligeti, Roberto Vera, Gergely Lukács, Balázs Győrffy, S. Pongor
{"title":"Predicting effective drug combinations via network propagation","authors":"B. Ligeti, Roberto Vera, Gergely Lukács, Balázs Győrffy, S. Pongor","doi":"10.1109/BioCAS.2013.6679718","DOIUrl":null,"url":null,"abstract":"Drug combinations are frequently used in treating complex diseases including cancer, diabetes, arthritis and hypertension. Most drug combinations were found in empirical ways so there is a need of efficient computational methods. Here we present a novel method based on network analysis which estimates the efficacy of drug combinations from a perturbation analysis performed on a protein-protein association network. The results suggest that those drugs are likely to form effective combinations that perturb a large number of proteins in common, even if the original targets are found in seemingly unrelated pathways.","PeriodicalId":344317,"journal":{"name":"2013 IEEE Biomedical Circuits and Systems Conference (BioCAS)","volume":"4 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2013-12-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"5","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"2013 IEEE Biomedical Circuits and Systems Conference (BioCAS)","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1109/BioCAS.2013.6679718","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 5
Abstract
Drug combinations are frequently used in treating complex diseases including cancer, diabetes, arthritis and hypertension. Most drug combinations were found in empirical ways so there is a need of efficient computational methods. Here we present a novel method based on network analysis which estimates the efficacy of drug combinations from a perturbation analysis performed on a protein-protein association network. The results suggest that those drugs are likely to form effective combinations that perturb a large number of proteins in common, even if the original targets are found in seemingly unrelated pathways.