Perturbation of energy metabolism by fatty-acid derivative AIC-47 and imatinib in BCR-ABL-harboring leukemic cells
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文摘

Imatinib strongly suppresses Warburg effect through the down-regulation of PTBP1.

Fatty-acid oxidation (FAO) supports glucose-independent survival in imatinib-treated cells.

Inactivation of BCR-ABL activates compensatory FAO.

AIC-47 perturbs both glycolysis and FAO.

The inhibition of glycolysis and FAO can be effective for the CD34+ fraction.

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