Although the treatment modalities for acute myeloid leukemia (AML) have not changed much over the past 40 years, distinct progress has been made in deciphering the basic biology underlying the pathogenesis of this group of hematological disorders. Studies show that AML development is a multicause, multistep and multipathway process. Accordingly, AMLs constitute a heterogeneous group of diseases. The thorough understanding of the molecular basis of AML is paving the way for better therapeutic approaches. Multiple novel drugs are being introduced and new, more efficient and less toxic formulations of conventional therapeutics are becoming available. Here, we review the recent advances in the comprehension of the molecular processes that lead to the onset of AML and its translation into clinical practice.

Understanding the molecular basis of acute myeloid leukemias : where are we now? / A. M Gruszka, D. Valli, M. Alcalay. - In: INTERNATIONAL JOURNAL OF HEMATOLOGIC ONCOLOGY. - ISSN 2045-1393. - 6:2(2017 Nov), pp. 43-53. [10.2217/ijh-2017-0002]

Understanding the molecular basis of acute myeloid leukemias : where are we now?

D. Valli
Secondo
;
M. Alcalay
Ultimo
2017

Abstract

Although the treatment modalities for acute myeloid leukemia (AML) have not changed much over the past 40 years, distinct progress has been made in deciphering the basic biology underlying the pathogenesis of this group of hematological disorders. Studies show that AML development is a multicause, multistep and multipathway process. Accordingly, AMLs constitute a heterogeneous group of diseases. The thorough understanding of the molecular basis of AML is paving the way for better therapeutic approaches. Multiple novel drugs are being introduced and new, more efficient and less toxic formulations of conventional therapeutics are becoming available. Here, we review the recent advances in the comprehension of the molecular processes that lead to the onset of AML and its translation into clinical practice.
AM;, leukemogenesis; molecular oncology
Settore MED/04 - Patologia Generale
Settore MED/03 - Genetica Medica
Settore MED/15 - Malattie del Sangue
nov-2017
Article (author)
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/551233
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