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10.1093/bib/bbab249

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suck abstract from ncbi


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pmid34245241      Brief+Bioinform 2021 ; 22 (6): ä
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  • Published anti-SARS-CoV-2 in vitro hits share common mechanisms of action that synergize with antivirals #MMPMID34245241
  • Xing J; Paithankar S; Liu K; Uhl K; Li X; Ko M; Kim S; Haskins J; Chen B
  • Brief Bioinform 2021[Nov]; 22 (6): ä PMID34245241show ga
  • The global efforts in the past year have led to the discovery of nearly 200 drug repurposing candidates for COVID-19. Gaining more insights into their mechanisms of action could facilitate a better understanding of infection and the development of therapeutics. Leveraging large-scale drug-induced gene expression profiles, we found 36% of the active compounds regulate genes related to cholesterol homeostasis and microtubule cytoskeleton organization. Following bioinformatics analyses revealed that the expression of these genes is associated with COVID-19 patient severity and has predictive power on anti-SARS-CoV-2 efficacy in vitro. Monensin, a top new compound that regulates these genes, was further confirmed as an inhibitor of SARS-CoV-2 replication in Vero-E6 cells. Interestingly, drugs co-targeting cholesterol homeostasis and microtubule cytoskeleton organization processes more likely present a synergistic effect with antivirals. Therefore, potential therapeutics could be centered around combinations of targeting these processes and viral proteins.
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