In patients with acute myeloid leukemia, cancer cells resist the effects of chemotherapy, many times resulting in disease recurrence and ultimately death.
‘The discovery of the mechanism under resistance to chemotherapy in leukemia reveals novel molecular targets that may be used to improve the efficiency of this type of treatment.’
The team, led by Sérgio Dias, had previously shown that leukemic cells activate certain molecular signals, namely a cell signaling pathway controlled by the Endothelial Vascular Growth Factor (VEGF), which allow cancer cells to survive despite chemotherapy.
The work revealed that a metabolic alteration at the mitochondrial level derived from VEGF's action is involved in chemotherapy resistance. By creating an experimental model of leukemia in mice whose cancer cells were resistant to chemotherapy the team was able to characterize these cells' metabolic profile and observed certain modifications at the level of the mitochondria.
Overcoming resistance to chemotherapy drugs
Using drugs that specifically blocked VEGF's activation, it was possible to revert these mitochondrial modifications and render these cells vulnerable to chemotherapy.
"Our study contributes to an improved understanding of how cellular metabolism plays an important role in the acquisition of resistance to certain therapeutic agents," said Sérgio Dias.
These newly discovered molecular targets will allow the development of therapeutic strategies that may be explored as possible routes to eliminate leukemic cells' resistance to chemotherapy.
- Sandrina Nóbrega-Pereira, Francisco Caiado et al. VEGFR-2-Mediated Reprogramming of Mitochondrial Metabolism Regulates the Sensitivity of Acute Myeloid Leukemia to Chemotherapy, Cancer Research DOI: 10.1158/0008-5472.CAN-17-1166