| Literature DB >> 34117734 |
Xiaoqi Wang1, Bin Xin1, Weihong Tan2, Zhijian Xu3, Kenli Li1, Fei Li4, Wu Zhong5, Shaoliang Peng1.
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.Entities:
Keywords: COVID-19; deep representation learning; drug discovery; excessive inflammatory response; heterogeneous drug networks
Year: 2021 PMID: 34117734 DOI: 10.1093/bib/bbab226
Source DB: PubMed Journal: Brief Bioinform ISSN: 1467-5463 Impact factor: 11.622