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10.1016/j.drudis.2021.11.002

http://scihub22266oqcxt.onion/10.1016/j.drudis.2021.11.002
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34763066!8574122!34763066
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suck abstract from ncbi


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pmid34763066      Drug+Discov+Today 2022 ; 27 (3): 848-856
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  • The PI3K/Akt/mTOR pathway: A potential pharmacological target in COVID-19 #MMPMID34763066
  • Basile MS; Cavalli E; McCubrey J; Hernandez-Bello J; Munoz-Valle JF; Fagone P; Nicoletti F
  • Drug Discov Today 2022[Mar]; 27 (3): 848-856 PMID34763066show ga
  • Coronavirus disease 2019 (COVID-19) has emerged as a serious threat to global health. The disregulation of the phosphatidylinositol 3-kinase/protein kinase B/mammalian target of rapamycin (PI3K/Akt/mTOR) cell signaling pathway observed in patients with COVID-19 has attracted attention for the possible use of specific inhibitors of this pathway for the treatment of the disease. Here, we review emerging data on the involvement of the PI3K/Akt/mTOR pathway in severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection and the clinical studies investigating its tailored inhibition in COVID-19. Current in silico, in vitro, and in vivo data convergently support a role for the PI3K/Akt/mTOR pathway in COVID-19 and suggest the use of specific inhibitors of this pathway that, by a combined mechanism entailing downregulation of excessive inflammatory reactions, cell protection, and antiviral effects, could ameliorate the course of COVID-19.
  • |*COVID-19 Drug Treatment[MESH]
  • |Animals[MESH]
  • |Antiviral Agents/*pharmacology[MESH]
  • |COVID-19/metabolism[MESH]
  • |Humans[MESH]
  • |Phosphatidylinositol 3-Kinases/*metabolism[MESH]
  • |Protein Kinase Inhibitors/*pharmacology[MESH]
  • |Proto-Oncogene Proteins c-akt/*metabolism[MESH]
  • |Signal Transduction/*drug effects[MESH]


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