Potential for Protein Kinase Pharmacological Regulation in Flaviviridae Infections.
Ana Belén BlázquezJuan Carlos SaizPublished in: International journal of molecular sciences (2020)
Protein kinases (PKs) are enzymes that catalyze the transfer of the terminal phosphate group from ATP to a protein acceptor, mainly to serine, threonine, and tyrosine residues. PK catalyzed phosphorylation is critical to the regulation of cellular signaling pathways that affect crucial cell processes, such as growth, differentiation, and metabolism. PKs represent attractive targets for drugs against a wide spectrum of diseases, including viral infections. Two different approaches are being applied in the search for antivirals: compounds directed against viral targets (direct-acting antivirals, DAAs), or against cellular components essential for the viral life cycle (host-directed antivirals, HDAs). One of the main drawbacks of DAAs is the rapid emergence of drug-resistant viruses. In contrast, HDAs present a higher barrier to resistance development. This work reviews the use of chemicals that target cellular PKs as HDAs against virus of the Flaviviridae family (Flavivirus and Hepacivirus), thus being potentially valuable therapeutic targets in the control of these pathogens.
Keyphrases
- protein kinase
- drug resistant
- sars cov
- life cycle
- multidrug resistant
- acinetobacter baumannii
- signaling pathway
- protein protein
- gram negative
- single cell
- magnetic resonance
- cell therapy
- systematic review
- stem cells
- randomized controlled trial
- binding protein
- pi k akt
- oxidative stress
- pseudomonas aeruginosa
- room temperature
- small molecule
- mesenchymal stem cells
- climate change
- cystic fibrosis
- genetic diversity
- quantum dots
- drug induced