Abstract
In this study, we investigated the synergistic effects of panobinostat and bortezomib on adriamycin-resistant HL60/ADR cells and refractory acute myelogenous leukemia (AML) primary cells. Combination of both agents had synergistic cytotoxicity on these cells, and increased the sensitivity of HL60/ADR cells to adriamycin. Panobinostat plus bortezomib was shown to modulate multiple apoptotic and drug metabolic related molecules, including activation of caspases, down-regulation of XIAP, Bcl-2 and MRP1. These effects were likely to be mediated via inhibition of AKT and NF-κB pathways. These findings provide evidence for clinic protocols using panobinostat and borezomib to overcome drug resistance in refractory AML patients.
Copyright © 2012 Elsevier Ireland Ltd. All rights reserved.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Acetylation
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Antineoplastic Agents / pharmacology
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Antineoplastic Agents / therapeutic use*
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Boronic Acids / pharmacology
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Boronic Acids / therapeutic use*
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Bortezomib
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Caspases / metabolism
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Drug Resistance, Neoplasm
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Drug Synergism
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HL-60 Cells
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Humans
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Hydroxamic Acids / pharmacology
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Hydroxamic Acids / therapeutic use*
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Indoles / pharmacology
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Indoles / therapeutic use*
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Leukemia, Myeloid, Acute / drug therapy*
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Leukemia, Myeloid, Acute / pathology
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NF-kappa B / metabolism*
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Panobinostat
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Poly(ADP-ribose) Polymerases / metabolism
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Proteolysis
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Proto-Oncogene Proteins c-akt / metabolism*
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Pyrazines / pharmacology
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Pyrazines / therapeutic use*
Substances
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Antineoplastic Agents
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Boronic Acids
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Hydroxamic Acids
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Indoles
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NF-kappa B
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Pyrazines
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Bortezomib
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Panobinostat
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Poly(ADP-ribose) Polymerases
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Proto-Oncogene Proteins c-akt
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Caspases