Network mirroring for drug repositioning

Abstract Background Although drug discoveries can provide meaningful insights and significant enhancements in pharmaceutical field, the longevity and cost that it takes can be extensive where the success rate is low. In order to circumvent the problem, there has been increased interest in ‘Drug Repo...

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Main Authors: Sunghong Park, Dong-gi Lee, Hyunjung Shin
Format: Article
Language:English
Published: BMC 2017-05-01
Series:BMC Medical Informatics and Decision Making
Subjects:
Online Access:http://link.springer.com/article/10.1186/s12911-017-0449-x
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spelling doaj-7e6e9db1063446a1a9ca0571bde975af2020-11-24T21:00:48ZengBMCBMC Medical Informatics and Decision Making1472-69472017-05-0117S111110.1186/s12911-017-0449-xNetwork mirroring for drug repositioningSunghong Park0Dong-gi Lee1Hyunjung Shin2Department of Industrial Engineering, Ajou UniversityDepartment of Industrial Engineering, Ajou UniversityDepartment of Industrial Engineering, Ajou UniversityAbstract Background Although drug discoveries can provide meaningful insights and significant enhancements in pharmaceutical field, the longevity and cost that it takes can be extensive where the success rate is low. In order to circumvent the problem, there has been increased interest in ‘Drug Repositioning’ where one searches for already approved drugs that have high potential of efficacy when applied to other diseases. To increase the success rate for drug repositioning, one considers stepwise screening and experiments based on biological reactions. Given the amount of drugs and diseases, however, the one-by-one procedure may be time consuming and expensive. Methods In this study, we propose a machine learning based approach for efficiently selecting candidate diseases and drugs. We assume that if two diseases are similar, then a drug for one disease can be effective against the other disease too. For the procedure, we first construct two disease networks; one with disease-protein association and the other with disease-drug information. If two networks are dissimilar, in a sense that the edge distribution of a disease node differ, it indicates high potential for repositioning new candidate drugs for that disease. The Kullback-Leibler divergence is employed to measure difference of connections in two constructed disease networks. Lastly, we perform repositioning of drugs to the top 20% ranked diseases. Results The results showed that F-measure of the proposed method was 0.75, outperforming 0.5 of greedy searching for the entire diseases. For the utility of the proposed method, it was applied to dementia and verified 75% accuracy for repositioned drugs assuming that there are not any known drugs to be used for dementia. Conclusion This research has novelty in that it discovers drugs with high potential of repositioning based on disease networks with the quantitative measure. Through the study, it is expected to produce profound insights for possibility of undiscovered drug repositioning.http://link.springer.com/article/10.1186/s12911-017-0449-xDrug repositioningDisease networkKullback-Leibler DivergenceSemi-Supervised Learning
collection DOAJ
language English
format Article
sources DOAJ
author Sunghong Park
Dong-gi Lee
Hyunjung Shin
spellingShingle Sunghong Park
Dong-gi Lee
Hyunjung Shin
Network mirroring for drug repositioning
BMC Medical Informatics and Decision Making
Drug repositioning
Disease network
Kullback-Leibler Divergence
Semi-Supervised Learning
author_facet Sunghong Park
Dong-gi Lee
Hyunjung Shin
author_sort Sunghong Park
title Network mirroring for drug repositioning
title_short Network mirroring for drug repositioning
title_full Network mirroring for drug repositioning
title_fullStr Network mirroring for drug repositioning
title_full_unstemmed Network mirroring for drug repositioning
title_sort network mirroring for drug repositioning
publisher BMC
series BMC Medical Informatics and Decision Making
issn 1472-6947
publishDate 2017-05-01
description Abstract Background Although drug discoveries can provide meaningful insights and significant enhancements in pharmaceutical field, the longevity and cost that it takes can be extensive where the success rate is low. In order to circumvent the problem, there has been increased interest in ‘Drug Repositioning’ where one searches for already approved drugs that have high potential of efficacy when applied to other diseases. To increase the success rate for drug repositioning, one considers stepwise screening and experiments based on biological reactions. Given the amount of drugs and diseases, however, the one-by-one procedure may be time consuming and expensive. Methods In this study, we propose a machine learning based approach for efficiently selecting candidate diseases and drugs. We assume that if two diseases are similar, then a drug for one disease can be effective against the other disease too. For the procedure, we first construct two disease networks; one with disease-protein association and the other with disease-drug information. If two networks are dissimilar, in a sense that the edge distribution of a disease node differ, it indicates high potential for repositioning new candidate drugs for that disease. The Kullback-Leibler divergence is employed to measure difference of connections in two constructed disease networks. Lastly, we perform repositioning of drugs to the top 20% ranked diseases. Results The results showed that F-measure of the proposed method was 0.75, outperforming 0.5 of greedy searching for the entire diseases. For the utility of the proposed method, it was applied to dementia and verified 75% accuracy for repositioned drugs assuming that there are not any known drugs to be used for dementia. Conclusion This research has novelty in that it discovers drugs with high potential of repositioning based on disease networks with the quantitative measure. Through the study, it is expected to produce profound insights for possibility of undiscovered drug repositioning.
topic Drug repositioning
Disease network
Kullback-Leibler Divergence
Semi-Supervised Learning
url http://link.springer.com/article/10.1186/s12911-017-0449-x
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