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Repurposing Didanosine as a Potential Treatment for COVID-19 Using Single-Cell RNA Sequencing Data

Fadhl Alakwaa

2020mSystems39 citationsDOIOpen Access PDF

Abstract

As of today (7 April 2020), more than 81,000 people around the world have died from the coronavirus disease 19 (COVID-19) pandemic. There is no approved drug or vaccine for COVID-19, although more than 10 clinical trials have been launched to test potential drugs. In an urgent response to this pandemic, I developed a bioinformatics pipeline to identify compounds and drug candidates to potentially treat COVID-19. This pipeline is based on publicly available single-cell RNA sequencing (scRNA-seq) data and the drug perturbation database "Library of Integrated Network-Based Cellular Signatures" (LINCS). I developed a ranking score system that prioritizes these drugs or small molecules. The four drugs with the highest total score are didanosine, benzyl-quinazolin-4-yl-amine, camptothecin, and RO-90-7501. In conclusion, I have demonstrated the utility of bioinformatics for identifying drugs than can be repurposed for potentially treating COVID-19 patients.

Topics & Concepts

RepurposingCoronavirus disease 2019 (COVID-19)DidanosineSevere acute respiratory syndrome coronavirus 2 (SARS-CoV-2)Virology2019-20 coronavirus outbreakRNADrug repositioningComputational biologyMedicineBiologyPharmacologyHuman immunodeficiency virus (HIV)Viral loadInternal medicineGeneticsAntiretroviral therapyDrugGeneInfectious disease (medical specialty)EcologyOutbreakDiseaseCOVID-19 Clinical Research StudiesSARS-CoV-2 and COVID-19 ResearchTuberculosis Research and Epidemiology
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