Metabolic reprogramming in childhood acute lymphoblastic leukemia.
Yordan SbirkovHasan BurnusuzovVictoria SarafianPublished in: Pediatric blood & cancer (2020)
The first observations of altered metabolism in malignant cells were made nearly 100 years ago and therapeutic strategies targeting cell metabolism have been in clinical use for several decades. In this review, we summarize our current understanding of cell metabolism dysregulation in childhood acute lymphoblastic leukemia (cALL). Reprogramming of cellular bioenergetic processes can be expected in the three distinct stages of cALL: at diagnosis, during standard chemotherapy, and in cases of relapse. Upregulation of glycolysis, dependency on anaplerotic energy sources, and activation of the electron transport chain have all been observed in cALL. While the current treatment strategies are tackling some of these aberrations, cALL cells are likely to be able to rewire their metabolism in order to escape therapy, which may contribute to a refractory disease and relapse. Finally, here we focus on novel therapeutic approaches emerging from our evolving understanding of the alterations of different metabolic networks in lymphoblasts.
Keyphrases
- acute lymphoblastic leukemia
- induced apoptosis
- cell cycle arrest
- single cell
- cell therapy
- allogeneic hematopoietic stem cell transplantation
- signaling pathway
- squamous cell carcinoma
- endoplasmic reticulum stress
- cell death
- poor prognosis
- oxidative stress
- mesenchymal stem cells
- childhood cancer
- copy number
- locally advanced
- drug delivery
- cancer therapy
- bone marrow
- acute myeloid leukemia
- drinking water
- replacement therapy