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DeSIDE-DDI: interpretable prediction of drug-drug interactions using drug-induced gene expressions

Adverse drug-drug interaction (DDI) is a major concern to polypharmacy due to its unexpected adverse side effects and must be identified at an early stage of drug discovery and development. Many computational methods have been proposed for this purpose, but most require specific types of information...

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Autores principales: Kim, Eunyoung, Nam, Hojung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8895921/
https://www.ncbi.nlm.nih.gov/pubmed/35246258
http://dx.doi.org/10.1186/s13321-022-00589-5
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author Kim, Eunyoung
Nam, Hojung
author_facet Kim, Eunyoung
Nam, Hojung
author_sort Kim, Eunyoung
collection PubMed
description Adverse drug-drug interaction (DDI) is a major concern to polypharmacy due to its unexpected adverse side effects and must be identified at an early stage of drug discovery and development. Many computational methods have been proposed for this purpose, but most require specific types of information, or they have less concern in interpretation on underlying genes. We propose a deep learning-based framework for DDI prediction with drug-induced gene expression signatures so that the model can provide the expression level of interpretability for DDIs. The model engineers dynamic drug features using a gating mechanism that mimics the co-administration effects by imposing attention to genes. Also, each side-effect is projected into a latent space through translating embedding. As a result, the model achieved an AUC of 0.889 and an AUPR of 0.915 in unseen interaction prediction, which is competitively very accurate and outperforms other state-of-the-art methods. Furthermore, it can predict potential DDIs with new compounds not used in training. In conclusion, using drug-induced gene expression signatures followed by gating and translating embedding can increase DDI prediction accuracy while providing model interpretability. The source code is available on GitHub (https://github.com/GIST-CSBL/DeSIDE-DDI). SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13321-022-00589-5.
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spelling pubmed-88959212022-03-10 DeSIDE-DDI: interpretable prediction of drug-drug interactions using drug-induced gene expressions Kim, Eunyoung Nam, Hojung J Cheminform Research Article Adverse drug-drug interaction (DDI) is a major concern to polypharmacy due to its unexpected adverse side effects and must be identified at an early stage of drug discovery and development. Many computational methods have been proposed for this purpose, but most require specific types of information, or they have less concern in interpretation on underlying genes. We propose a deep learning-based framework for DDI prediction with drug-induced gene expression signatures so that the model can provide the expression level of interpretability for DDIs. The model engineers dynamic drug features using a gating mechanism that mimics the co-administration effects by imposing attention to genes. Also, each side-effect is projected into a latent space through translating embedding. As a result, the model achieved an AUC of 0.889 and an AUPR of 0.915 in unseen interaction prediction, which is competitively very accurate and outperforms other state-of-the-art methods. Furthermore, it can predict potential DDIs with new compounds not used in training. In conclusion, using drug-induced gene expression signatures followed by gating and translating embedding can increase DDI prediction accuracy while providing model interpretability. The source code is available on GitHub (https://github.com/GIST-CSBL/DeSIDE-DDI). SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13321-022-00589-5. Springer International Publishing 2022-03-04 /pmc/articles/PMC8895921/ /pubmed/35246258 http://dx.doi.org/10.1186/s13321-022-00589-5 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Kim, Eunyoung
Nam, Hojung
DeSIDE-DDI: interpretable prediction of drug-drug interactions using drug-induced gene expressions
title DeSIDE-DDI: interpretable prediction of drug-drug interactions using drug-induced gene expressions
title_full DeSIDE-DDI: interpretable prediction of drug-drug interactions using drug-induced gene expressions
title_fullStr DeSIDE-DDI: interpretable prediction of drug-drug interactions using drug-induced gene expressions
title_full_unstemmed DeSIDE-DDI: interpretable prediction of drug-drug interactions using drug-induced gene expressions
title_short DeSIDE-DDI: interpretable prediction of drug-drug interactions using drug-induced gene expressions
title_sort deside-ddi: interpretable prediction of drug-drug interactions using drug-induced gene expressions
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8895921/
https://www.ncbi.nlm.nih.gov/pubmed/35246258
http://dx.doi.org/10.1186/s13321-022-00589-5
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