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CODA:用于分析药物效应的多层次面向上下文的定向关联集成。

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

机构信息

Department of Bio and Brain Engineering, KAIST, 291 Daehak-ro, Yuseong-gu, Daejeon, Republic of Korea.

Bio-Synergy Research Center, 291 Daehak-ro, Yuseong-gu, 305- 701, Daejeon, Republic of Korea.

出版信息

Sci Rep. 2017 Aug 8;7(1):7519. doi: 10.1038/s41598-017-07448-6.

DOI:10.1038/s41598-017-07448-6
PMID:28790372
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5548804/
Abstract

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.

摘要

基于网络的计算方法在药物开发领域显示出了很有前景的结果。然而,尽管生物关联实际上确实出现在特定的环境中,但之前的研究中使用的大多数网络都没有包含环境信息。在这里,我们使用蛋白质表达数据和科学文献为生物关联分配环境,从而重新构建一个解剖环境特定网络。此外,我们使用环境特定网络来分析药物作用,方法是在药物靶点和疾病之间使用接近度度量。与之前的环境特定网络不同,我们的网络中包含了细胞间关联和表型水平实体,如生物过程,以代表人体。观察到通过添加环境信息和表型水平实体,推断药物-疾病关联的性能得到了提高。特别是,详细分析了与多个器官相关并与多个表型水平实体相关的疾病高血压,以研究我们的网络如何促进药物-疾病关联的推断。我们的结果表明,包含环境信息、细胞间关联和表型水平实体可以有助于更好地预测药物-疾病关联,并提供对药物如何影响人体疾病的理解的详细见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/390f/5548804/2873d2440113/41598_2017_7448_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/390f/5548804/bb3758c6d61e/41598_2017_7448_Fig1_HTML.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/390f/5548804/09ac9b519b75/41598_2017_7448_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/390f/5548804/6a5f72ec2e68/41598_2017_7448_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/390f/5548804/58f9e0bd21f2/41598_2017_7448_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/390f/5548804/2873d2440113/41598_2017_7448_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/390f/5548804/bb3758c6d61e/41598_2017_7448_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/390f/5548804/60f2bd13d7f5/41598_2017_7448_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/390f/5548804/b97fb7191b17/41598_2017_7448_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/390f/5548804/09ac9b519b75/41598_2017_7448_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/390f/5548804/6a5f72ec2e68/41598_2017_7448_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/390f/5548804/58f9e0bd21f2/41598_2017_7448_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/390f/5548804/2873d2440113/41598_2017_7448_Fig7_HTML.jpg

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