Targeting Proliferation Signals and the Cell Cycle Machinery in Acute Leukemias: Novel Molecules on the Horizon

Uncontrolled proliferative signals and cell cycle dysregulation due to genomic or functional alterations are important drivers of the expansion of undifferentiated blast cells in acute myeloid leukemia (AML) and acute lymphoblastic leukemia (ALL) cells. Therefore, they are largely studied as potential therapeutic targets in the field. We here present the most recent advancements in the evaluation of novel compounds targeting cell cycle proteins or oncogenic mechanisms, including those showing an antiproliferative effect in acute leukemia, independently of the identification of a specific target. Several new kinase inhibitors have been synthesized that showed effectiveness in a nanomolar to micromolar concentration range as inhibitors of FLT3 and its mutant forms, a highly attractive therapeutic target due to its driver role in a significant fraction of AML cases. Moreover, we introduce novel molecules functioning as microtubule-depolymerizing or P53-restoring agents, G-quadruplex-stabilizing molecules and CDK2, CHK1, PI3K delta, STAT5, BRD4 and BRPF1 inhibitors. We here discuss their mechanisms of action, including the downstream intracellular changes induced by in vitro treatment, hematopoietic toxicity, in vivo bio-availability and efficacy in murine xenograft models. The promising activity profile demonstrated by some of these candidates deserves further development towards clinical investigation.

Automated summary

Uncontrolled proliferative signals and cell cycle dysregulation are important drivers of leukemia, and new compounds targeting cell cycle proteins and oncogenic mechanisms show promising therapeutic potential. The development of kinase inhibitors, microtubule-depolymerizing agents, P53-restoring agents, G-quadruplex-stabilizing molecules, and inhibitors of CDK2, CHK1, PI3K delta, STAT5, BRD4, and BRPF1 have shown effectiveness in inhibiting leukemia growth. Further investigation is needed to evaluate their toxicity, bio-availability, and efficacy in clinical settings.