Willems, L; Chapuis, N; Puissant, A; Maciel, T T; Green, A S; Jacque, N; Vignon, C; Park, S; Guichard, S; Herault, O; Fricot, A; Hermine, O; Moura, I C; Auberger, P; Ifrah, N; Dreyfus, F; Bonnet, D; Lacombe, C; Mayeux, P; Bouscary, D; Tamburini, J
The serine/threonine kinase mammalian target of rapamycin (mTOR) is crucial for cell growth and proliferation, and is constitutively activated in primary acute myeloid leukemia (AML) cells, therefore representing a major target for drug development in this disease. We show here that the specific mTOR kinase inhibitor AZD8055 blocked mTORC1 and mTORC2 signaling in AML. Particularly, AZD8055 fully inhibited multisite eIF4E-binding protein 1 phosphorylation, subsequently blocking protein translation, which was in contrast to the effects of rapamycin. In addition, the mTORC1-dependent PI3K/Akt feedback activation was fully abrogated in AZD8055-treated AML cells. Significantly, AZD8055 decreased AML blast cell proliferation and cell cycle progression, reduced the clonogenic growth of leukemic progenitors and induced caspase-dependent apoptosis in leukemic cells but not in normal immature CD34+ cells. Interestingly, AZD8055 strongly induced autophagy, which may be either protective or cell death inducing, depending on concentration. Finally, AZD8055 markedly increased the survival of AML transplanted mice through a significant reduction of tumor growth, without apparent toxicity. Our current results strongly suggest that AZD8055 should be tested in AML patients in clinical trials.
Diseases/Pathways annotated by Medline MESH:
Leukemia, Myeloid, Acute
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Text Mining Data
PI3K/Akt → mTORC1: " In addition, the mTORC1
feedback activation was fully abrogated in AZD8055 treated AML cells "
PI3K/Akt → mTORC1: " In addition, the mTORC1 dependent PI3K/Akt feedback activation was fully abrogated in AZD8055 treated AML cells "
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