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A cancer drug atlas enables synergistic targeting of independent drug vulnerabilities.

Ravi S NarayanPiet MolenaarJian TengFleur M G CornelissenIrene RoelofsRenee MenezesRogier DikTonny LagerweijYoran BroersmaNaomi PetersenJhon Alexander Marin SotoEelke BrandsPhilip van KuikenMaria C LeccaKristiaan J LenosSjors G J G In 't VeldWessel van WieringenFrederick F LangErik P SulmanRoel G W VerhaakBrigitta Gertrud BaumertLukas J A StalpersLouis VermeulenColin WattsDavid Stanley BaileyBen J SlotmanRogier VersteegDavid NoskePeter SminiaBakhos A TannousTom WurdingerJan KosterBart A Westerman
Published in: Nature communications (2020)
Personalized cancer treatments using combinations of drugs with a synergistic effect is attractive but proves to be highly challenging. Here we present an approach to uncover the efficacy of drug combinations based on the analysis of mono-drug effects. For this we used dose-response data from pharmacogenomic encyclopedias and represent these as a drug atlas. The drug atlas represents the relations between drug effects and allows to identify independent processes for which the tumor might be particularly vulnerable when attacked by two drugs. Our approach enables the prediction of combination-therapy which can be linked to tumor-driving mutations. By using this strategy, we can uncover potential effective drug combinations on a pan-cancer scale. Predicted synergies are provided and have been validated in glioblastoma, breast cancer, melanoma and leukemia mouse-models, resulting in therapeutic synergy in 75% of the tested models. This indicates that we can accurately predict effective drug combinations with translational value.
Keyphrases
  • drug induced
  • combination therapy
  • adverse drug
  • single cell
  • emergency department
  • squamous cell carcinoma
  • machine learning
  • squamous cell
  • acute myeloid leukemia
  • artificial intelligence
  • climate change