Suppressing IKZF1 Deletion-Mediated Activation of Ras Oncogenic Signaling By the Combination of Azacitidine and Flumatinib in High-Risk B-ALL

Background IKZF1 deletion is frequently observed in Ph + acute lymphoblastic leukemia (Ph + ALL), which results in poor prognosis and affects clinical efficacy, and possible resistance to tyrosine kinase inhibitors (TKIs). Ikaros transcriptionally regulates the gene expression of multiple oncogenic pathways including Ras/MAPK signaling. However, it is undefined about the role of IKZF1 genetic defects in the activation of Ras/MAPK signaling and their relations with the efficacy of therapeutic drugs in ALL. This study is to investigate the sensitivity of IKZF1-deletion-mediated activation of RAS signaling to the new combined therapy of TKI Flumatinib (FLU) and the Azacitidine (AZA) in B-ALL cells. Methods The patients' samples were obtained from Zhongda Hospital Southeast University with the approval of the institute's Ethics Committee. The gene expression was tested by qPCR or Western blot. CCK8 Cell proliferation, PI staining cell cycle analysis, and apoptosis assay (Annexin V-FITC/ PI staining) were performed in SUP-B15, the Ph + ALL cells with IKZF1 deletion treated with DMSO control, FLU only, AZA only, and FLU+AZA. The overlapped differential expression genes (DEGs）with the pathways (GO term, KEGG) analysis and gene interaction networks were achieved in the potential oncogenic genes in ALL through databases (OMIM, TTD, and GeneCards), and drug targets over that of SwissTargetPrediction, SuperPred, and SEA. Results AZA or FLU treatment induced the cell proliferation arrest of SUP-B15 cells in a dose-/time-dependent manner (Fig. 1A). The combination of IC50 AZA with various doses of FLU significantly enhanced the effect on cell proliferation arrest versus single-drug controls, and CalcuSyn analysis demonstrated their synergistic effect in the cells (Fig. 1B). Also, the combination significantly increased the G0/G1 phase arrest (Fig. 1C, D), and % of apoptotic cells (Fig. 1E, F) versus the single-drug controls. Consistently, the combination up-regulated the mRNA and protein levels of P53, BAX, and P21, but decreased the MDM2, BCL2, and CyclinE (Fig. 1G, H). A total of 118 overlapped DEGs were identified between the potential oncogenes in ALL and FLU-/AZA-associated genes, and they predominantly enriched in Ras/MAPK oncogenic pathways, in which PTPN11 is at the top of the pathways. Indeed, the combination significantly decreased the mRNA and protein levels of PTPN11 (Fig. 2A, B). PTPN11 is significantly higher expressed in 20 newly-diagnosed Ph +ALL patien