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CODA: Integrating multi-level context-oriented directed associations for analysis of drug effects

In silico network-based methods have shown promising results in the field of drug development. Yet, most of networks used in the previous research have not included context information even though biological associations actually do appear in the specific contexts. Here, we reconstruct an anatomical...

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Autores principales: Yu, Hasun, Jung, Jinmyung, Yoon, Seyeol, Kwon, Mijin, Bae, Sunghwa, Yim, Soorin, Lee, Jaehyun, Kim, Seunghyun, Kang, Yeeok, Lee, Doheon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5548804/
https://www.ncbi.nlm.nih.gov/pubmed/28790372
http://dx.doi.org/10.1038/s41598-017-07448-6
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author Yu, Hasun
Jung, Jinmyung
Yoon, Seyeol
Kwon, Mijin
Bae, Sunghwa
Yim, Soorin
Lee, Jaehyun
Kim, Seunghyun
Kang, Yeeok
Lee, Doheon
author_facet Yu, Hasun
Jung, Jinmyung
Yoon, Seyeol
Kwon, Mijin
Bae, Sunghwa
Yim, Soorin
Lee, Jaehyun
Kim, Seunghyun
Kang, Yeeok
Lee, Doheon
author_sort Yu, Hasun
collection PubMed
description In silico network-based methods have shown promising results in the field of drug development. Yet, most of networks used in the previous research have not included context information even though biological associations actually do appear in the specific contexts. Here, we reconstruct an anatomical context-specific network by assigning contexts to biological associations using protein expression data and scientific literature. Furthermore, we employ the context-specific network for the analysis of drug effects with a proximity measure between drug targets and diseases. Distinct from previous context-specific networks, intercellular associations and phenomic level entities such as biological processes are included in our network to represent the human body. It is observed that performances in inferring drug-disease associations are increased by adding context information and phenomic level entities. In particular, hypertension, a disease related to multiple organs and associated with several phenomic level entities, is analyzed in detail to investigate how our network facilitates the inference of drug-disease associations. Our results indicate that the inclusion of context information, intercellular associations, and phenomic level entities can contribute towards a better prediction of drug-disease associations and provide detailed insight into understanding of how drugs affect diseases in the human body.
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spelling pubmed-55488042017-08-09 CODA: Integrating multi-level context-oriented directed associations for analysis of drug effects Yu, Hasun Jung, Jinmyung Yoon, Seyeol Kwon, Mijin Bae, Sunghwa Yim, Soorin Lee, Jaehyun Kim, Seunghyun Kang, Yeeok Lee, Doheon Sci Rep Article In silico network-based methods have shown promising results in the field of drug development. Yet, most of networks used in the previous research have not included context information even though biological associations actually do appear in the specific contexts. Here, we reconstruct an anatomical context-specific network by assigning contexts to biological associations using protein expression data and scientific literature. Furthermore, we employ the context-specific network for the analysis of drug effects with a proximity measure between drug targets and diseases. Distinct from previous context-specific networks, intercellular associations and phenomic level entities such as biological processes are included in our network to represent the human body. It is observed that performances in inferring drug-disease associations are increased by adding context information and phenomic level entities. In particular, hypertension, a disease related to multiple organs and associated with several phenomic level entities, is analyzed in detail to investigate how our network facilitates the inference of drug-disease associations. Our results indicate that the inclusion of context information, intercellular associations, and phenomic level entities can contribute towards a better prediction of drug-disease associations and provide detailed insight into understanding of how drugs affect diseases in the human body. Nature Publishing Group UK 2017-08-08 /pmc/articles/PMC5548804/ /pubmed/28790372 http://dx.doi.org/10.1038/s41598-017-07448-6 Text en © The Author(s) 2017 Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Yu, Hasun
Jung, Jinmyung
Yoon, Seyeol
Kwon, Mijin
Bae, Sunghwa
Yim, Soorin
Lee, Jaehyun
Kim, Seunghyun
Kang, Yeeok
Lee, Doheon
CODA: Integrating multi-level context-oriented directed associations for analysis of drug effects
title CODA: Integrating multi-level context-oriented directed associations for analysis of drug effects
title_full CODA: Integrating multi-level context-oriented directed associations for analysis of drug effects
title_fullStr CODA: Integrating multi-level context-oriented directed associations for analysis of drug effects
title_full_unstemmed CODA: Integrating multi-level context-oriented directed associations for analysis of drug effects
title_short CODA: Integrating multi-level context-oriented directed associations for analysis of drug effects
title_sort coda: integrating multi-level context-oriented directed associations for analysis of drug effects
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5548804/
https://www.ncbi.nlm.nih.gov/pubmed/28790372
http://dx.doi.org/10.1038/s41598-017-07448-6
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