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DeepR2cov:基于异质药物网络的深度学习表示学习,以发现用于 COVID-19 的抗炎药物。

DeepR2cov: deep representation learning on heterogeneous drug networks to discover anti-inflammatory agents for COVID-19.

机构信息

College of Computer Science and Electronic Engineering, Hunan University, China.

Chinese Academy of Sciences in the College of Chemistry and Chemical Engineering, College of Biology, Hunan University, China.

出版信息

Brief Bioinform. 2021 Nov 5;22(6). doi: 10.1093/bib/bbab226.

Abstract

Recent studies have demonstrated that the excessive inflammatory response is an important factor of death in coronavirus disease 2019 (COVID-19) patients. In this study, we propose a deep representation on heterogeneous drug networks, termed DeepR2cov, to discover potential agents for treating the excessive inflammatory response in COVID-19 patients. This work explores the multi-hub characteristic of a heterogeneous drug network integrating eight unique networks. Inspired by the multi-hub characteristic, we design 3 billion special meta paths to train a deep representation model for learning low-dimensional vectors that integrate long-range structure dependency and complex semantic relation among network nodes. Based on the representation vectors and transcriptomics data, we predict 22 drugs that bind to tumor necrosis factor-α or interleukin-6, whose therapeutic associations with the inflammation storm in COVID-19 patients, and molecular binding model are further validated via data from PubMed publications, ongoing clinical trials and a docking program. In addition, the results on five biomedical applications suggest that DeepR2cov significantly outperforms five existing representation approaches. In summary, DeepR2cov is a powerful network representation approach and holds the potential to accelerate treatment of the inflammatory responses in COVID-19 patients. The source code and data can be downloaded from https://github.com/pengsl-lab/DeepR2cov.git.

摘要

最近的研究表明,过度的炎症反应是导致 2019 年冠状病毒病(COVID-19)患者死亡的一个重要因素。在这项研究中,我们提出了一种基于异构药物网络的深度表示方法,称为 DeepR2cov,以发现治疗 COVID-19 患者过度炎症反应的潜在药物。这项工作探索了整合了八个独特网络的异构药物网络的多枢纽特征。受多枢纽特征的启发,我们设计了 30 亿条特殊元路径来训练深度表示模型,以学习整合网络节点之间远程结构依赖和复杂语义关系的低维向量。基于表示向量和转录组学数据,我们预测了 22 种与肿瘤坏死因子-α或白细胞介素-6 结合的药物,其与 COVID-19 患者炎症风暴的治疗关联以及分子结合模型通过 PubMed 出版物、正在进行的临床试验和对接程序的数据得到了进一步验证。此外,五项生物医学应用的结果表明,DeepR2cov 显著优于五种现有表示方法。总之,DeepR2cov 是一种强大的网络表示方法,有可能加速 COVID-19 患者炎症反应的治疗。源代码和数据可从 https://github.com/pengsl-lab/DeepR2cov.git 下载。

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