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Open AccessReview

Targeting Tyrosine Kinases in Acute Myeloid Leukemia: Why, Who and How?

Institut National de la Santé et de la Recherche Médicale, U1035 Bordeaux, France
Université de Bordeaux, 33076 Bordeaux, France
CHU Bordeaux, Service d’Hématologie Clinique et Thérapie Cellulaire, F-33000 Bordeaux, France
Author to whom correspondence should be addressed.
Int. J. Mol. Sci. 2019, 20(14), 3429;
Received: 21 June 2019 / Revised: 8 July 2019 / Accepted: 10 July 2019 / Published: 12 July 2019
(This article belongs to the Special Issue Drug Resistance in Hematologic Malignancies)
PDF [686 KB, uploaded 12 July 2019]
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Acute myeloid leukemia (AML) is a myeloid malignancy carrying a heterogeneous molecular panel of mutations participating in the blockade of differentiation and the increased proliferation of myeloid hematopoietic stem and progenitor cells. The historical “3 + 7” treatment (cytarabine and daunorubicin) is currently challenged by new therapeutic strategies, including drugs depending on the molecular landscape of AML. This panel of mutations makes it possible to combine some of these new treatments with conventional chemotherapy. For example, the FLT3 receptor is overexpressed or mutated in 80% or 30% of AML, respectively. Such anomalies have led to the development of targeted therapies using tyrosine kinase inhibitors (TKIs). In this review, we document the history of TKI targeting, FLT3 and several other tyrosine kinases involved in dysregulated signaling pathways. View Full-Text
Keywords: acute myeloid leukemia; tyrosine kinase; inhibitors; targeted therapy acute myeloid leukemia; tyrosine kinase; inhibitors; targeted therapy

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This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited (CC BY 4.0).

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Fernandez, S.; Desplat, V.; Villacreces, A.; Guitart, A.V.; Milpied, N.; Pigneux, A.; Vigon, I.; Pasquet, J.-M.; Dumas, P.-Y. Targeting Tyrosine Kinases in Acute Myeloid Leukemia: Why, Who and How? Int. J. Mol. Sci. 2019, 20, 3429.

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