Quantitative phosphoproteomics uncovers synergy between DNA-PK and FLT3 inhibitors in acute myeloid leukaemia

Leukemia. 2021 Jun;35(6):1782-1787. doi: 10.1038/s41375-020-01050-y. Epub 2020 Oct 16.
No abstract available

Publication types

  • Letter
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Benzothiazoles / pharmacology*
  • Chromones / pharmacology*
  • DNA-Activated Protein Kinase / antagonists & inhibitors*
  • Drug Synergism*
  • Drug Therapy, Combination
  • Humans
  • Leukemia, Myeloid, Acute / drug therapy*
  • Leukemia, Myeloid, Acute / metabolism
  • Leukemia, Myeloid, Acute / pathology
  • Morpholines / pharmacology*
  • Phenylurea Compounds / pharmacology*
  • Phosphoproteins / metabolism*
  • Proteome / drug effects*
  • Tumor Cells, Cultured
  • fms-Like Tyrosine Kinase 3 / antagonists & inhibitors*

Substances

  • 8-dibenzothiophen-4-yl-2-morpholin-4-yl-chromen-4-one
  • Benzothiazoles
  • Chromones
  • Morpholines
  • Phenylurea Compounds
  • Phosphoproteins
  • Proteome
  • quizartinib
  • FLT3 protein, human
  • fms-Like Tyrosine Kinase 3
  • DNA-Activated Protein Kinase