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Comprehensive assessment of side effects in COVID-19 drug pipeline from a network perspective

Currently, coronavirus disease 2019 (COVID-19), has posed an imminent threat to global public health. Although some current therapeutic agents have showed potential prevention or treatment, a growing number of associated adverse events have occurred on patients with COVID-19 in the course of medical...

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Autores principales: Wu, Qihui, Fan, Xiude, Hong, Honghai, Gu, Yong, Liu, Zhihong, Fang, Shuhuan, Wang, Qi, Cai, Chuipu, Fang, Jiansong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Ltd. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7505223/
https://www.ncbi.nlm.nih.gov/pubmed/32971210
http://dx.doi.org/10.1016/j.fct.2020.111767
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author Wu, Qihui
Fan, Xiude
Hong, Honghai
Gu, Yong
Liu, Zhihong
Fang, Shuhuan
Wang, Qi
Cai, Chuipu
Fang, Jiansong
author_facet Wu, Qihui
Fan, Xiude
Hong, Honghai
Gu, Yong
Liu, Zhihong
Fang, Shuhuan
Wang, Qi
Cai, Chuipu
Fang, Jiansong
author_sort Wu, Qihui
collection PubMed
description Currently, coronavirus disease 2019 (COVID-19), has posed an imminent threat to global public health. Although some current therapeutic agents have showed potential prevention or treatment, a growing number of associated adverse events have occurred on patients with COVID-19 in the course of medical treatment. Therefore, a comprehensive assessment of the safety profile of therapeutic agents against COVID-19 is urgently needed. In this study, we proposed a network-based framework to identify the potential side effects of current COVID-19 drugs in clinical trials. We established the associations between 116 COVID-19 drugs and 30 kinds of human tissues based on network proximity and gene-set enrichment analysis (GSEA) approaches. Additionally, we focused on four types of drug-induced toxicities targeting four tissues, including hepatotoxicity, renal toxicity, lung toxicity, and neurotoxicity, and validated our network-based predictions by preclinical and clinical evidence available. Finally, we further performed pharmacovigilance analysis to validate several drug-tissue toxicities via data mining adverse event reporting data, and we identified several new drug-induced side effects without labeling in Food and Drug Administration (FDA) drug instructions. Overall, this study provides forceful approaches to assess potential side effects on COVID-19 drugs, which will be helpful for their safe use in clinical practice and promoting the discovery of antiviral therapeutics against SARS-CoV-2.
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spelling pubmed-75052232020-09-23 Comprehensive assessment of side effects in COVID-19 drug pipeline from a network perspective Wu, Qihui Fan, Xiude Hong, Honghai Gu, Yong Liu, Zhihong Fang, Shuhuan Wang, Qi Cai, Chuipu Fang, Jiansong Food Chem Toxicol Article Currently, coronavirus disease 2019 (COVID-19), has posed an imminent threat to global public health. Although some current therapeutic agents have showed potential prevention or treatment, a growing number of associated adverse events have occurred on patients with COVID-19 in the course of medical treatment. Therefore, a comprehensive assessment of the safety profile of therapeutic agents against COVID-19 is urgently needed. In this study, we proposed a network-based framework to identify the potential side effects of current COVID-19 drugs in clinical trials. We established the associations between 116 COVID-19 drugs and 30 kinds of human tissues based on network proximity and gene-set enrichment analysis (GSEA) approaches. Additionally, we focused on four types of drug-induced toxicities targeting four tissues, including hepatotoxicity, renal toxicity, lung toxicity, and neurotoxicity, and validated our network-based predictions by preclinical and clinical evidence available. Finally, we further performed pharmacovigilance analysis to validate several drug-tissue toxicities via data mining adverse event reporting data, and we identified several new drug-induced side effects without labeling in Food and Drug Administration (FDA) drug instructions. Overall, this study provides forceful approaches to assess potential side effects on COVID-19 drugs, which will be helpful for their safe use in clinical practice and promoting the discovery of antiviral therapeutics against SARS-CoV-2. Elsevier Ltd. 2020-11 2020-09-21 /pmc/articles/PMC7505223/ /pubmed/32971210 http://dx.doi.org/10.1016/j.fct.2020.111767 Text en © 2020 Elsevier Ltd. 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
Wu, Qihui
Fan, Xiude
Hong, Honghai
Gu, Yong
Liu, Zhihong
Fang, Shuhuan
Wang, Qi
Cai, Chuipu
Fang, Jiansong
Comprehensive assessment of side effects in COVID-19 drug pipeline from a network perspective
title Comprehensive assessment of side effects in COVID-19 drug pipeline from a network perspective
title_full Comprehensive assessment of side effects in COVID-19 drug pipeline from a network perspective
title_fullStr Comprehensive assessment of side effects in COVID-19 drug pipeline from a network perspective
title_full_unstemmed Comprehensive assessment of side effects in COVID-19 drug pipeline from a network perspective
title_short Comprehensive assessment of side effects in COVID-19 drug pipeline from a network perspective
title_sort comprehensive assessment of side effects in covid-19 drug pipeline from a network perspective
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7505223/
https://www.ncbi.nlm.nih.gov/pubmed/32971210
http://dx.doi.org/10.1016/j.fct.2020.111767
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