Abstract
Compound 48 (C48) is a novel dual ligand for peroxisome proliferator-activated receptor alpha and gamma (PPAR alpha/gamma). Culture of imatinib-sensitive and -resistant CML cell lines with C48 resulted in a strong growth inhibition which associated with G0/G1 cell cycle arrest. However, it showed no obvious toxicity to normal CD34(+) hematopoietic stem cells. Decrease of pSTATs and pAKT were noticed suggesting that interference of AKT and STATs signaling may be the mechanisms for the effects of PPAR alpha/gamma ligands. Of more clinical importance, this ligand strongly enhanced the anticancer-effects of imatinib. Overall, our data suggest that the PPAR alpha/gamma ligands may have potentials in the treatment of CML in an adjuvant setting either before or after the development of imatinib resistance.
Publication types
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Research Support, N.I.H., Extramural
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Research Support, Non-U.S. Gov't
MeSH terms
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Antineoplastic Agents / pharmacology*
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Antineoplastic Agents / therapeutic use
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Apoptosis / drug effects
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Benzamides
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Benzopyrans / pharmacology*
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Blotting, Western
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Cell Cycle / drug effects
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Cell Division / drug effects*
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Cell Line, Tumor
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Cell Proliferation / drug effects
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Humans
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Imatinib Mesylate
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Leukemia, Myelogenous, Chronic, BCR-ABL Positive / drug therapy*
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Leukemia, Myelogenous, Chronic, BCR-ABL Positive / metabolism
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Leukemia, Myelogenous, Chronic, BCR-ABL Positive / pathology
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Ligands
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PPAR alpha / metabolism*
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PPAR gamma / metabolism*
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Piperazines / pharmacology*
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Piperazines / therapeutic use
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Pyrimidines / pharmacology*
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Pyrimidines / therapeutic use
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Reverse Transcriptase Polymerase Chain Reaction
Substances
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Antineoplastic Agents
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Benzamides
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Benzopyrans
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Ligands
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PPAR alpha
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PPAR gamma
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Piperazines
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Pyrimidines
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Imatinib Mesylate