Targeting glycometabolic reprogramming to restore the sensitivity of leukemia drug-resistant K562/ADM cells to adriamycin

Life Sci. 2018 Dec 15:215:1-10. doi: 10.1016/j.lfs.2018.10.050. Epub 2018 Oct 25.

Abstract

Aims: Mounting studies have confirmed that cancer cells reprogram their metabolism during early carcinogenesis to develop many other hallmarks, and demonstrated a relationship between aerobic glycolysis and the occurrence of drug resistance. However, the molecular mechanisms and role in tumor drug resistance of aerobic glycolysis remain unclear.

Main methods: We analyzed differentially expressed genes (DEGs) at the RNA level between the multi-drug resistance (MDR) leukemia cell line K562/adriamycin (ADM) and its parental, drug-sensitive K562 cell line. Clustering and enrichment analysis of DEGs was performed. Oxamate, a lactic dehydrogenase inhibitor were used to assess the effect of glycolysis inhibition on ADM susceptibility and the expression of the enriched DEGs in K562/ADM cells.

Key findings: A total of 1742 DEGs were detected between the K562/ADM and K562 cell lines. The differential expression of unigenes encoding enzymes involved in glycometabolism signifies that there was a greater aerobic glycolysis flux in K562/ADM cells. The PI3K-AKT signaling pathway, which is related to glucose metabolism, showed representative differential enrichment and up-regulation in K562/ADM cells. Oxamate improved and re-sensitized the therapeutic effect of ADM in ADM-resistant cells by inhibiting aerobic glycolysis either directly or indirectly by down-regulation of the AKT-mTOR pathway.

Significance: Our findings suggest that ADM resistance mediated by the increase of aerobic glycolysis, which related to the over-activation of the AKT-mTOR-c-Myc pathway in MDR leukemia cells. Inhibition of aerobic glycolysis and down-regulation of signaling pathways involved in aerobic glycolysis represent a potential chemotherapeutic strategy for sensitizing leukemic cells and thereby overcoming MDR.

Keywords: Aerobic glycolysis; Glycolysis inhibitor; Glycometabolic reprogramming; Leukemia; Multi-drug resistance.

MeSH terms

  • Carcinogenesis
  • Cellular Reprogramming*
  • Cluster Analysis
  • Doxorubicin / administration & dosage*
  • Drug Resistance, Multiple / genetics
  • Drug Resistance, Neoplasm / genetics*
  • Drug Screening Assays, Antitumor
  • Drug Synergism
  • Gene Expression Profiling
  • Gene Expression Regulation, Leukemic
  • Glycolysis
  • Humans
  • K562 Cells
  • L-Lactate Dehydrogenase / antagonists & inhibitors
  • Leukemia / drug therapy*
  • Oxamic Acid / administration & dosage*
  • Phosphatidylinositol 3-Kinases / metabolism

Substances

  • Doxorubicin
  • L-Lactate Dehydrogenase
  • Phosphatidylinositol 3-Kinases
  • Oxamic Acid