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

Author

Listed:
  • Theodore P. Braun

    (Oregon Health & Science University
    Oregon Health & Science University)

  • Mariam Okhovat

    (Oregon Health & Science University)

  • Cody Coblentz

    (Oregon Health & Science University
    Oregon Health & Science University)

  • Sarah A. Carratt

    (Oregon Health & Science University
    Oregon Health & Science University)

  • Amy Foley

    (Oregon Health & Science University
    Oregon Health & Science University)

  • Zachary Schonrock

    (Oregon Health & Science University
    Oregon Health & Science University)

  • Brittany M. Curtiss

    (Oregon Health & Science University
    Oregon Health & Science University)

  • Kimberly Nevonen

    (Oregon Health & Science University)

  • Brett Davis

    (Oregon Health & Science University)

  • Brianna Garcia

    (Oregon Health & Science University
    Oregon Health & Science University)

  • Dorian LaTocha

    (Oregon Health & Science University
    Oregon Health & Science University)

  • Benjamin R. Weeder

    (Oregon Health & Science University)

  • Michal R. Grzadkowski

    (Oregon Health & Science University)

  • Joey C. Estabrook

    (Oregon Health & Science University)

  • Hannah G. Manning

    (Oregon Health & Science University)

  • Kevin Watanabe-Smith

    (Oregon Health & Science University
    Oregon Health & Science University)

  • Sophia Jeng

    (Oregon Health & Science University)

  • Jenny L. Smith

    (Fred Hutchinson Cancer Research Center)

  • Amanda R. Leonti

    (Fred Hutchinson Cancer Research Center)

  • Rhonda E. Ries

    (Fred Hutchinson Cancer Research Center)

  • Shannon McWeeney

    (Oregon Health & Science University
    Oregon Health & Science University)

  • Cristina Genua

    (John Radcliffe Hospital)

  • Roy Drissen

    (John Radcliffe Hospital)

  • Claus Nerlov

    (John Radcliffe Hospital)

  • Soheil Meshinchi

    (Fred Hutchinson Cancer Research Center
    University of Washington)

  • Lucia Carbone

    (Oregon Health & Science University
    Oregon Health & Science University
    Oregon Health & Science University)

  • Brian J. Druker

    (Oregon Health & Science University
    Oregon Health & Science University
    Howard Hughes Medical Institute)

  • Julia E. Maxson

    (Oregon Health & Science University
    Oregon Health & Science University)

Abstract

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.

Suggested Citation

  • Theodore P. Braun & Mariam Okhovat & Cody Coblentz & Sarah A. Carratt & Amy Foley & Zachary Schonrock & Brittany M. Curtiss & Kimberly Nevonen & Brett Davis & Brianna Garcia & Dorian LaTocha & Benjami, 2019. "Myeloid lineage enhancers drive oncogene synergy in CEBPA/CSF3R mutant acute myeloid leukemia," Nature Communications, Nature, vol. 10(1), pages 1-15, December.
  • Handle: RePEc:nat:natcom:v:10:y:2019:i:1:d:10.1038_s41467-019-13364-2
    DOI: 10.1038/s41467-019-13364-2
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    Cited by:

    1. Dongmei Wang & Tao Sun & Yuan Xia & Zhe Zhao & Xue Sheng & Shuying Li & Yuechan Ma & Mingying Li & Xiuhua Su & Fan Zhang & Peng Li & Daoxin Ma & Jingjing Ye & Fei Lu & Chunyan Ji, 2023. "Homodimer-mediated phosphorylation of C/EBPα-p42 S16 modulates acute myeloid leukaemia differentiation through liquid-liquid phase separation," Nature Communications, Nature, vol. 14(1), pages 1-16, December.

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