A Hyperactive Signalosome in Acute Myeloid Leukemia Drives Addiction to a Tumor-Specific Hsp90 Species Academic Article uri icon


MeSH Major

  • HSP90 Heat-Shock Proteins
  • Leukemia, Myeloid, Acute
  • Signal Transduction


  • Acute myeloid leukemia (AML) is a heterogeneous and fatal disease with an urgent need for improved therapeutic regimens given that most patients die from relapsed disease. Irrespective of mutation status, the development of aggressive leukemias is enabled by increasing dependence on signaling networks. We demonstrate that a hyperactive signalosome drives addiction of AML cells to a tumor-specific Hsp90 species (teHsp90). Through genetic, environmental, and pharmacologic perturbations, we demonstrate a direct and quantitative link between hyperactivated signaling pathways and apoptotic sensitivity of AML to teHsp90 inhibition. Specifically, we find that hyperactive JAK-STAT and PI3K-AKT signaling networks are maintained by teHsp90 and, in fact, gradual activation of these networks drives tumors increasingly dependent on teHsp90. Thus, although clinically aggressive AML survives via signalosome activation, this addiction creates a vulnerability that can be exploited with Hsp90-directed therapy.

publication date

  • December 15, 2015



  • Academic Article



  • eng

PubMed Central ID

  • PMC4699804

Digital Object Identifier (DOI)

  • 10.1016/j.celrep.2015.10.073

PubMed ID

  • 26628369

Additional Document Info

start page

  • 2159

end page

  • 73


  • 13


  • 10