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Myeloid lineage enhancers drive oncogene synergy in CEBPA/CSF3R mutant acute myeloid leukemia.

Theodore P BraunMariam OkhovatCody CoblentzSarah A CarrattAmy FoleyZachary SchonrockBrittany M SmithKimberly NevonenBrett A DavisBrianna GarciaDorian LaTochaBenjamin R WeederMichal R GrzadkowskiJoey C EstabrookHannah G ManningKevin Watanabe-SmithSophia JengJenny L SmithAmanda R LeontiRhonda E RiesShannon K McWeeneyCristina Di GenuaRoy DrissenClaus NerlovSoheil MeshinchiLucia CarboneBrian J DrukerJulia E Maxson
Published in: Nature communications (2019)
Acute Myeloid Leukemia (AML) develops due to the acquisition of mutations from multiple functional classes. Here, we demonstrate that activating mutations in the granulocyte colony stimulating factor receptor (CSF3R), cooperate with loss of function mutations in the transcription factor CEBPA to promote acute leukemia development. The interaction between these distinct classes of mutations occurs at the level of myeloid lineage enhancers where mutant CEBPA prevents activation of a subset of differentiation associated enhancers. To confirm this enhancer-dependent mechanism, we demonstrate that CEBPA mutations must occur as the initial event in AML initiation. This improved mechanistic understanding will facilitate therapeutic development targeting the intersection of oncogene cooperativity.
Keyphrases
  • acute myeloid leukemia
  • transcription factor
  • allogeneic hematopoietic stem cell transplantation
  • dendritic cells
  • bone marrow
  • signaling pathway
  • immune response
  • acute lymphoblastic leukemia
  • wild type