Activation of FGFR1β signaling pathway promotes survival, migration and resistance to chemotherapy in acute myeloid leukemia cells Academic Article uri icon


MeSH Major

  • Cell Movement
  • Drug Resistance, Neoplasm
  • Leukemia, Myeloid
  • Receptor, Fibroblast Growth Factor, Type 1
  • Signal Transduction


  • Fibroblast growth factors (FGFs) are important regulators of hematopoiesis and have been implicated in the tumorigenesis of solid tumors. Recent evidence suggests that FGF signaling through FGF receptors (FGFRs) may play a role in the proliferation of subsets of acute myeloid leukemias (AMLs). However, the precise mechanism and specific FGF receptors that support leukemic cell growth are not known. We show that FGF-2, through activation of FGFR1beta signaling, promotes survival, proliferation and migration of AML cells. Stimulation of FGFR1beta results in phosphoinositide 3-kinase (PI3-K)/Akt activation and inhibits chemotherapy-induced apoptosis of leukemic cells. Neutralizing FGFR1-specific antibody abrogates the physiologic and chemoprotective effects of FGF-2/FGFR1beta signaling and inhibits tumor growth in mice xenotransplanted with human AML. These data suggest that activation of FGF-2/FGFR1beta supports progression and chemoresistance in subsets of AML. Therefore, FGFR1 targeting may be of therapeutic benefit in subsets of AML.

publication date

  • June 2006



  • Academic Article



  • eng

Digital Object Identifier (DOI)

  • 10.1038/sj.leu.2404203

PubMed ID

  • 16598308

Additional Document Info

start page

  • 979

end page

  • 86


  • 20


  • 6