Peer-Reviewed Journal Details
Mandatory Fields
Rishi, L,Hannon, M,Salome, M,Hasemann, M,Frank, AK,Campos, J,Timoney, J,O'Connor, C,Cahill, MR,Porse, B,Keeshan, K
2014
April
Blood
Regulation of Trib2 by an E2F1-C/EBP alpha feedback loop in AML cell proliferation
Validated
Optional Fields
ACUTE MYELOID-LEUKEMIA ACUTE LYMPHOBLASTIC-LEUKEMIA ACUTE MYELOGENOUS LEUKEMIA GENE-EXPRESSION PROFILES C/EBP-ALPHA IN-VIVO CEBPA MUTATIONS FAMILY-MEMBERS CYCLE CONTROL C-MYC
123
2389
2400
The loss of regulation of cell proliferation is a key event in leukemic transformation, and the oncogene tribbles (Trib)2 is emerging as a pivotal target of transcription factors in acute leukemias. Deregulation of the transcription factor E2F1, normally repressed by CCAAT enhancer-binding protein a (C/EBP alpha)-p42, occurs in acute myeloid leukemia (AML), resulting in the perturbation of cell cycle and apoptosis, emphasizing its importance in the molecular pathogenesis of AML. Here we show that E2F family members directly regulate Trib2 in leukemic cells and identify a feedback regulatory loop for E2F1, C/EBP alpha, and Trib2 inAML cell proliferation and survival. Further analyses revealed that E2F1-mediated Trib2 expression was repressed by C/EBP alpha-p42, and in normal granulocyte/macrophage progenitor cells, we detect C/EBP alpha bound to the Trib2 promoter. Pharmacological inhibition of the cell cycle or Trib2 knockdown resulted in a block in AML cell proliferation. Our work proposes a novel paradigm whereby E2F1 plays a key role in the regulation of Trib2 expression important for AML cell proliferation control. Importantly, we identify the contribution of dysregulated C/EBP alpha and E2F1 to elevated Trib2 expression and leukemic cell survival, which likely contributes to the initiation and maintenance of AML and may have significant implications for normal and malignant hematopoiesis.
10.1182/blood-2013-07-511683
Grant Details