Cargando…
Network mirroring for drug repositioning
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 Repositionin...
Autores principales: | , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5444046/ https://www.ncbi.nlm.nih.gov/pubmed/28539121 http://dx.doi.org/10.1186/s12911-017-0449-x |
_version_ | 1783238667248074752 |
---|---|
author | Park, Sunghong Lee, Dong-gi Shin, Hyunjung |
author_facet | Park, Sunghong Lee, Dong-gi Shin, Hyunjung |
author_sort | Park, Sunghong |
collection | PubMed |
description | 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. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12911-017-0449-x) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5444046 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-54440462017-05-25 Network mirroring for drug repositioning Park, Sunghong Lee, Dong-gi Shin, Hyunjung BMC Med Inform Decis Mak Research 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. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12911-017-0449-x) contains supplementary material, which is available to authorized users. BioMed Central 2017-05-18 /pmc/articles/PMC5444046/ /pubmed/28539121 http://dx.doi.org/10.1186/s12911-017-0449-x Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Park, Sunghong Lee, Dong-gi Shin, Hyunjung Network mirroring for drug repositioning |
title | 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_short | Network mirroring for drug repositioning |
title_sort | network mirroring for drug repositioning |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5444046/ https://www.ncbi.nlm.nih.gov/pubmed/28539121 http://dx.doi.org/10.1186/s12911-017-0449-x |
work_keys_str_mv | AT parksunghong networkmirroringfordrugrepositioning AT leedonggi networkmirroringfordrugrepositioning AT shinhyunjung networkmirroringfordrugrepositioning |