The Role of AMPK/mTOR Modulators in the Therapy of Acute Myeloid Leukemia
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Published:2019-07-01
Issue:12
Volume:26
Page:2208-2229
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ISSN:0929-8673
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Container-title:Current Medicinal Chemistry
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language:en
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Short-container-title:CMC
Author:
Visnjic Dora1, Dembitz Vilma1, Lalic Hrvoje1
Affiliation:
1. Department of Physiology and Croatian Institute for Brain Research, School of Medicine, University of Zagreb, Salata 12, 10 000 Zagreb, Croatia
Abstract
Differentiation therapy of acute promyelocytic leukemia with all-trans retinoic
acid represents the most successful pharmacological therapy of acute myeloid leukemia
(AML). Numerous studies demonstrate that drugs that inhibit mechanistic target of rapamycin
(mTOR) and activate AMP-kinase (AMPK) have beneficial effects in promoting
differentiation and blocking proliferation of AML. Most of these drugs are already in use
for other purposes; rapalogs as immunosuppressants, biguanides as oral antidiabetics, and
5-amino-4-imidazolecarboxamide ribonucleoside (AICAr, acadesine) as an exercise mimetic.
Although most of these pharmacological modulators have been widely used for
decades, their mechanism of action is only partially understood. In this review, we summarize
the role of AMPK and mTOR in hematological malignancies and discuss the possible
role of pharmacological modulators in proliferation and differentiation of leukemia
cells.
Funder
Operational Programme Competitiveness European Regional Development Fund Croatian Science Foundation
Publisher
Bentham Science Publishers Ltd.
Subject
Pharmacology,Molecular Medicine,Drug Discovery,Biochemistry,Organic Chemistry
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