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Context-specific functional module based drug efficacy prediction

BACKGROUND: It is necessary to evaluate the efficacy of individual drugs on patients to realize personalized medicine. Testing drugs on patients in clinical trial is the only way to evaluate the efficacy of drugs. The approach is labour intensive and requires overwhelming costs and a number of exper...

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Autores principales: Hwang, Woochang, Choi, Jaejoon, Kwon, Mijin, Lee, Doheon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4965733/
https://www.ncbi.nlm.nih.gov/pubmed/27490093
http://dx.doi.org/10.1186/s12859-016-1078-6
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author Hwang, Woochang
Choi, Jaejoon
Kwon, Mijin
Lee, Doheon
author_facet Hwang, Woochang
Choi, Jaejoon
Kwon, Mijin
Lee, Doheon
author_sort Hwang, Woochang
collection PubMed
description BACKGROUND: It is necessary to evaluate the efficacy of individual drugs on patients to realize personalized medicine. Testing drugs on patients in clinical trial is the only way to evaluate the efficacy of drugs. The approach is labour intensive and requires overwhelming costs and a number of experiments. Therefore, preclinical model system has been intensively investigated for predicting the efficacy of drugs. Current computational drug sensitivity prediction approaches use general biological network modules as their prediction features. Therefore, they miss indirect effectors or the effects from tissue-specific interactions. RESULTS: We developed cell line specific functional modules. Enriched scores of functional modules are utilized as cell line specific features to predict the efficacy of drugs. Cell line specific functional modules are clusters of genes, which have similar biological functions in cell line specific networks. We used linear regression for drug efficacy prediction. We assessed the prediction performance in leave-one-out cross-validation (LOOCV). Our method was compared with elastic net model, which is a popular model for drug efficacy prediction. In addition, we analysed drug sensitivity-associated functions of five drugs - lapatinib, erlotinib, raloxifene, tamoxifen and gefitinib- by our model. CONCLUSIONS: Our model can provide cell line specific drug efficacy prediction and also provide functions which are associated with drug sensitivity. Therefore, we could utilize drug sensitivity associated functions for drug repositioning or for suggesting secondary drugs for overcoming drug resistance. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12859-016-1078-6) contains supplementary material, which is available to authorized users.
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spelling pubmed-49657332016-08-02 Context-specific functional module based drug efficacy prediction Hwang, Woochang Choi, Jaejoon Kwon, Mijin Lee, Doheon BMC Bioinformatics Research BACKGROUND: It is necessary to evaluate the efficacy of individual drugs on patients to realize personalized medicine. Testing drugs on patients in clinical trial is the only way to evaluate the efficacy of drugs. The approach is labour intensive and requires overwhelming costs and a number of experiments. Therefore, preclinical model system has been intensively investigated for predicting the efficacy of drugs. Current computational drug sensitivity prediction approaches use general biological network modules as their prediction features. Therefore, they miss indirect effectors or the effects from tissue-specific interactions. RESULTS: We developed cell line specific functional modules. Enriched scores of functional modules are utilized as cell line specific features to predict the efficacy of drugs. Cell line specific functional modules are clusters of genes, which have similar biological functions in cell line specific networks. We used linear regression for drug efficacy prediction. We assessed the prediction performance in leave-one-out cross-validation (LOOCV). Our method was compared with elastic net model, which is a popular model for drug efficacy prediction. In addition, we analysed drug sensitivity-associated functions of five drugs - lapatinib, erlotinib, raloxifene, tamoxifen and gefitinib- by our model. CONCLUSIONS: Our model can provide cell line specific drug efficacy prediction and also provide functions which are associated with drug sensitivity. Therefore, we could utilize drug sensitivity associated functions for drug repositioning or for suggesting secondary drugs for overcoming drug resistance. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12859-016-1078-6) contains supplementary material, which is available to authorized users. BioMed Central 2016-07-28 /pmc/articles/PMC4965733/ /pubmed/27490093 http://dx.doi.org/10.1186/s12859-016-1078-6 Text en © Hwang et al. 2016 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
Hwang, Woochang
Choi, Jaejoon
Kwon, Mijin
Lee, Doheon
Context-specific functional module based drug efficacy prediction
title Context-specific functional module based drug efficacy prediction
title_full Context-specific functional module based drug efficacy prediction
title_fullStr Context-specific functional module based drug efficacy prediction
title_full_unstemmed Context-specific functional module based drug efficacy prediction
title_short Context-specific functional module based drug efficacy prediction
title_sort context-specific functional module based drug efficacy prediction
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4965733/
https://www.ncbi.nlm.nih.gov/pubmed/27490093
http://dx.doi.org/10.1186/s12859-016-1078-6
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