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SANE: A sequence combined attentive network embedding model for COVID-19 drug repositioning

The COVID-19 has now spread all over the world and causes a huge burden for public health and world economy. Drug repositioning has become a promising treatment strategy in COVID-19 crisis because it can shorten drug development process, reduce pharmaceutical costs and reposition approval drugs. Exi...

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Autores principales: Su, Xiaorui, You, Zhuhong, Wang, Lei, Hu, Lun, Wong, Leon, Ji, Boya, Zhao, Bowei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier B.V. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8381638/
https://www.ncbi.nlm.nih.gov/pubmed/34456656
http://dx.doi.org/10.1016/j.asoc.2021.107831
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author Su, Xiaorui
You, Zhuhong
Wang, Lei
Hu, Lun
Wong, Leon
Ji, Boya
Zhao, Bowei
author_facet Su, Xiaorui
You, Zhuhong
Wang, Lei
Hu, Lun
Wong, Leon
Ji, Boya
Zhao, Bowei
author_sort Su, Xiaorui
collection PubMed
description The COVID-19 has now spread all over the world and causes a huge burden for public health and world economy. Drug repositioning has become a promising treatment strategy in COVID-19 crisis because it can shorten drug development process, reduce pharmaceutical costs and reposition approval drugs. Existing computational methods only focus on single information, such as drug and virus similarity or drug–virus network feature, which is not sufficient to predict potential drugs. In this paper, a sequence combined attentive network embedding model SANE is proposed for identifying drugs based on sequence features and network features. On the one hand, drug SMILES and virus sequence features are extracted by encoder–decoder in SANE as node initial embedding in drug–virus network. On the other hand, SANE obtains fields for each node by attention-based Depth-First-Search (DFS) to reduce noises and improve efficiency in representation learning and adopts a bottom-up aggregation strategy to learn node network representation from selected fields. Finally, a forward neural network is used for classifying. Experiment results show that SANE has achieved the performance with 81.98% accuracy and 0.8961 AUC value and outperformed state-of-the-art baselines. Further case study on COVID-19 indicates that SANE has a strong predictive ability since 25 of the top 40 (62.5%) drugs are verified by valuable dataset and literatures. Therefore, SANE is powerful to reposition drugs for COVID-19 and provides a new perspective for drug repositioning.
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spelling pubmed-83816382021-08-23 SANE: A sequence combined attentive network embedding model for COVID-19 drug repositioning Su, Xiaorui You, Zhuhong Wang, Lei Hu, Lun Wong, Leon Ji, Boya Zhao, Bowei Appl Soft Comput Article The COVID-19 has now spread all over the world and causes a huge burden for public health and world economy. Drug repositioning has become a promising treatment strategy in COVID-19 crisis because it can shorten drug development process, reduce pharmaceutical costs and reposition approval drugs. Existing computational methods only focus on single information, such as drug and virus similarity or drug–virus network feature, which is not sufficient to predict potential drugs. In this paper, a sequence combined attentive network embedding model SANE is proposed for identifying drugs based on sequence features and network features. On the one hand, drug SMILES and virus sequence features are extracted by encoder–decoder in SANE as node initial embedding in drug–virus network. On the other hand, SANE obtains fields for each node by attention-based Depth-First-Search (DFS) to reduce noises and improve efficiency in representation learning and adopts a bottom-up aggregation strategy to learn node network representation from selected fields. Finally, a forward neural network is used for classifying. Experiment results show that SANE has achieved the performance with 81.98% accuracy and 0.8961 AUC value and outperformed state-of-the-art baselines. Further case study on COVID-19 indicates that SANE has a strong predictive ability since 25 of the top 40 (62.5%) drugs are verified by valuable dataset and literatures. Therefore, SANE is powerful to reposition drugs for COVID-19 and provides a new perspective for drug repositioning. Elsevier B.V. 2021-11 2021-08-23 /pmc/articles/PMC8381638/ /pubmed/34456656 http://dx.doi.org/10.1016/j.asoc.2021.107831 Text en © 2021 Elsevier B.V. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Su, Xiaorui
You, Zhuhong
Wang, Lei
Hu, Lun
Wong, Leon
Ji, Boya
Zhao, Bowei
SANE: A sequence combined attentive network embedding model for COVID-19 drug repositioning
title SANE: A sequence combined attentive network embedding model for COVID-19 drug repositioning
title_full SANE: A sequence combined attentive network embedding model for COVID-19 drug repositioning
title_fullStr SANE: A sequence combined attentive network embedding model for COVID-19 drug repositioning
title_full_unstemmed SANE: A sequence combined attentive network embedding model for COVID-19 drug repositioning
title_short SANE: A sequence combined attentive network embedding model for COVID-19 drug repositioning
title_sort sane: a sequence combined attentive network embedding model for covid-19 drug repositioning
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8381638/
https://www.ncbi.nlm.nih.gov/pubmed/34456656
http://dx.doi.org/10.1016/j.asoc.2021.107831
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