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A network paradigm predicts drug synergistic effects using downstream protein-protein interactions.

Jennifer L WilsonEthan SteinbergRebecca RaczRuss B AltmanNigam ShahKevin Grimes
Published in: CPT: pharmacometrics & systems pharmacology (2022)
In some cases, drug combinations affect adverse outcome phenotypes by binding the same protein; however, drug-binding proteins are associated through protein-protein interaction (PPI) networks within the cell, suggesting that drug phenotypes may result from long-range network effects. We first used PPI network analysis to classify drugs based on proteins downstream of their targets and next predicted drug combination effects where drugs shared network proteins but had distinct binding proteins (e.g., targets, enzymes, or transporters). By classifying drugs using their downstream proteins, we had an 80.7% sensitivity for predicting rare drug combination effects documented in gold-standard datasets. We further measured the effect of predicted drug combinations on adverse outcome phenotypes using novel observational studies in the electronic health record. We tested predictions for 60 network-drug classes on seven adverse outcomes and measured changes in clinical outcomes for predicted combinations. These results demonstrate a novel paradigm for anticipating drug synergistic effects using proteins downstream of drug targets.
Keyphrases
  • adverse drug
  • protein protein
  • network analysis
  • stem cells
  • emergency department
  • drug delivery
  • mesenchymal stem cells
  • cancer therapy
  • amino acid
  • dna binding