Oncogene-Induced Reprogramming in Acute Lymphoblastic Leukemia: Towards Targeted Therapy of Leukemia-Initiating Cells.
Vincent FregonaManon BayetBastien GerbyPublished in: Cancers (2021)
Our understanding of the hierarchical structure of acute leukemia has yet to be fully translated into therapeutic approaches. Indeed, chemotherapy still has to take into account the possibility that leukemia-initiating cells may have a distinct chemosensitivity profile compared to the bulk of the tumor, and therefore are spared by the current treatment, causing the relapse of the disease. Therefore, the identification of the cell-of-origin of leukemia remains a longstanding question and an exciting challenge in cancer research of the last few decades. With a particular focus on acute lymphoblastic leukemia, we present in this review the previous and current concepts exploring the phenotypic, genetic and functional heterogeneity in patients. We also discuss the benefits of using engineered mouse models to explore the early steps of leukemia development and to identify the biological mechanisms driving the emergence of leukemia-initiating cells. Finally, we describe the major prospects for the discovery of new therapeutic strategies that specifically target their aberrant stem cell-like functions.
Keyphrases
- acute lymphoblastic leukemia
- induced apoptosis
- acute myeloid leukemia
- bone marrow
- stem cells
- cell cycle arrest
- ejection fraction
- end stage renal disease
- small molecule
- endoplasmic reticulum stress
- mouse model
- mesenchymal stem cells
- signaling pathway
- squamous cell carcinoma
- chronic kidney disease
- newly diagnosed
- gene expression
- neuropathic pain
- patient reported outcomes
- copy number
- papillary thyroid
- diabetic rats
- drug induced
- radiation therapy
- locally advanced
- endothelial cells
- peritoneal dialysis
- squamous cell