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10.3390/metabo11100699

http://scihub22266oqcxt.onion/10.3390/metabo11100699
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34677415!8540749!34677415
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suck abstract from ncbi


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pmid34677415      Metabolites 2021 ; 11 (10): ä
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  • Targeting the Pentose Phosphate Pathway for SARS-CoV-2 Therapy #MMPMID34677415
  • Bojkova D; Costa R; Reus P; Bechtel M; Jaboreck MC; Olmer R; Martin U; Ciesek S; Michaelis M; Cinatl J Jr
  • Metabolites 2021[Oct]; 11 (10): ä PMID34677415show ga
  • SARS-CoV-2 is causing the coronavirus disease 2019 (COVID-19) pandemic, for which effective pharmacological therapies are needed. SARS-CoV-2 induces a shift of the host cell metabolism towards glycolysis, and the glycolysis inhibitor 2-deoxy-d-glucose (2DG), which interferes with SARS-CoV-2 infection, is under development for the treatment of COVID-19 patients. The glycolytic pathway generates intermediates that supply the non-oxidative branch of the pentose phosphate pathway (PPP). In this study, the analysis of proteomics data indicated increased transketolase (TKT) levels in SARS-CoV-2-infected cells, suggesting that a role is played by the non-oxidative PPP. In agreement, the TKT inhibitor benfooxythiamine (BOT) inhibited SARS-CoV-2 replication and increased the anti-SARS-CoV-2 activity of 2DG. In conclusion, SARS-CoV-2 infection is associated with changes in the regulation of the PPP. The TKT inhibitor BOT inhibited SARS-CoV-2 replication and increased the activity of the glycolysis inhibitor 2DG. Notably, metabolic drugs like BOT and 2DG may also interfere with COVID-19-associated immunopathology by modifying the metabolism of immune cells in addition to inhibiting SARS-CoV-2 replication. Hence, they may improve COVID-19 therapy outcomes by exerting antiviral and immunomodulatory effects.
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