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Glucose metabolism as a potential therapeutic target in Cytarabine-resistant acute Myeloid leukemia
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Orientador(es)
Resumo(s)
Altered glycolytic metabolism has been associated with chemoresistance in acute myeloid leukemia (AML). However, there are still aspects that need clarification, as well as how to explore these metabolic alterations in therapy. In the present study, we aimed to elucidate the role of glucose metabolism in the acquired resistance of AML cells to cytarabine (Ara-C) and to explore it as a therapeutic target. Resistance was induced by stepwise exposure of AML cells to increasing concentrations of Ara-C. Ara-C-resistant cells were characterized for their growth capacity, genetic alterations, metabolic profile, and sensitivity to different metabolic inhibitors. Ara-C-resistant AML cell lines, KG-1 Ara-R, and MOLM13 Ara-R presented different metabolic profiles. KG-1 Ara-R cells exhibited a more pronounced glycolytic phenotype than parental cells, with a weaker acute response to 3-bromopyruvate (3-BP) but higher sensitivity after 48 h. KG-1 Ara-R cells also display increased respiration rates and are more sensitive to phenformin than parental cells. On the other hand, MOLM13 Ara-R cells display a glucose metabolism profile similar to parental cells, as well as sensitivity to glycolytic inhibitors. These results indicate that acquired resistance to Ara-C in AML may involve metabolic adaptations, which can be explored therapeutically in the AML patient setting who developed resistance to therapy.
Descrição
Palavras-chave
Chemoresistance Cytarabine Acute myeloid leukemia Metabolic inhibitors Seahorse Glucose metabolism 3-bromopyruvate Phenformin
Contexto Educativo
Citação
Pereira-Vieira, J., Weber, D. D., Silva, S., Barbosa-Matos, C., Granja, S., Reis, R. M., Queirós, O., Ko, Y. H., Kofler, B., Casal, M., & Baltazar, F. (2024). Glucose metabolism as a potential therapeutic target in Cytarabine-resistant acute myeloid leukemia. Pharmaceutics, 16(4), Artigo 4. https://doi.org/10.3390/pharmaceutics16040442
Editora
MDPI