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Computational analysis to repurpose drugs for COVID-19 based on transcriptional response of host cells to SARS-CoV-2.
Li, Fuhai; Michelson, Andrew P; Foraker, Randi; Zhan, Ming; Payne, Philip R O.
  • Li F; Institute for Informatics (I2), Washington University in St. Louis School of Medicine, St. Louis, MO, USA. Fuhai.Li@wustl.edu.
  • Michelson AP; Department of Pediatrics, Washington University in St. Louis School of Medicine, St. Louis, MO, USA. Fuhai.Li@wustl.edu.
  • Foraker R; Institute for Informatics (I2), Washington University in St. Louis School of Medicine, St. Louis, MO, USA.
  • Zhan M; Pulmonary and Critical Care Medicine, Washington University in St. Louis School of Medicine, St. Louis, MO, USA.
  • Payne PRO; Institute for Informatics (I2), Washington University in St. Louis School of Medicine, St. Louis, MO, USA.
BMC Med Inform Decis Mak ; 21(1): 15, 2021 01 07.
Article in English | MEDLINE | ID: covidwho-1015860
ABSTRACT

BACKGROUND:

The Coronavirus Disease 2019 (COVID-19) pandemic has infected over 10 million people globally with a relatively high mortality rate. There are many therapeutics undergoing clinical trials, but there is no effective vaccine or therapy for treatment thus far. After affected by the Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2), molecular signaling pathways of host cells play critical roles during the life cycle of SARS-CoV-2. Thus, it is significant to identify the involved molecular signaling pathways within the host cells. Drugs targeting these molecular signaling pathways could be potentially effective for COVID-19 treatment.

METHODS:

In this study, we developed a novel integrative analysis approach to identify the related molecular signaling pathways within host cells, and repurposed drugs as potentially effective treatments for COVID-19, based on the transcriptional response of host cells.

RESULTS:

We identified activated signaling pathways associated with the infection caused SARS-CoV-2 in human lung epithelial cells through integrative analysis. Then, the activated gene ontologies (GOs) and super GOs were identified. Signaling pathways and GOs such as MAPK, JNK, STAT, ERK, JAK-STAT, IRF7-NFkB signaling, and MYD88/CXCR6 immune signaling were particularly activated. Based on the identified signaling pathways and GOs, a set of potentially effective drugs were repurposed by integrating the drug-target and reverse gene expression data resources. In addition to many drugs being evaluated in clinical trials, the dexamethasone was top-ranked in the prediction, which was the first reported drug to be able to significantly reduce the death rate of COVID-19 patients receiving respiratory support.

CONCLUSIONS:

The integrative genomics data analysis and results can be helpful to understand the associated molecular signaling pathways within host cells, and facilitate the discovery of effective drugs for COVID-19 treatment.
Subject(s)

Full text: Available Collection: International databases Database: MEDLINE Main subject: Transcription, Genetic / Pharmaceutical Preparations / Signal Transduction / Drug Repositioning / COVID-19 Drug Treatment Type of study: Experimental Studies / Prognostic study Topics: Vaccines Limits: Humans Language: English Journal: BMC Med Inform Decis Mak Journal subject: Medical Informatics Year: 2021 Document Type: Article Affiliation country: S12911-020-01373-x

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Transcription, Genetic / Pharmaceutical Preparations / Signal Transduction / Drug Repositioning / COVID-19 Drug Treatment Type of study: Experimental Studies / Prognostic study Topics: Vaccines Limits: Humans Language: English Journal: BMC Med Inform Decis Mak Journal subject: Medical Informatics Year: 2021 Document Type: Article Affiliation country: S12911-020-01373-x