CEBPA-mutated leukemia is sensitive to genetic and pharmacological targeting of the MLL1 complex.
Luisa SchmidtElizabeth HeyesLisa ScheibleckerThomas EderGiacomo VolpeJon FramptonClaus NerlovPeter ValentJolanta GrembeckaFlorian GrebienPublished in: Leukemia (2019)
The gene encoding the transcription factor C/EBPα is mutated in 10-15% of acute myeloid leukemia (AML) patients. N-terminal CEBPA mutations cause ablation of full-length C/EBPα without affecting the expression of a shorter oncogenic isoform, termed p30. The mechanistic basis of p30-induced leukemogenesis is incompletely understood. Here, we demonstrate that the MLL1 histone-methyltransferase complex represents a critical actionable vulnerability in CEBPA-mutated AML. Oncogenic C/EBPα p30 and MLL1 show global co-localization on chromatin and p30 exhibits robust physical interaction with the MLL1 complex. CRISPR/Cas9-mediated mutagenesis of MLL1 results in proliferation arrest and myeloid differentiation in C/EBPα p30-expressing cells. In line, CEBPA-mutated hematopoietic progenitor cells are hypersensitive to pharmacological targeting of the MLL1 complex. Inhibitor treatment impairs proliferation and restores myeloid differentiation potential in mouse and human AML cells with CEBPA mutations. Finally, we identify the transcription factor GATA2 as a direct critical target of the p30-MLL1 interaction. Altogether, we show that C/EBPα p30 requires the MLL1 complex to regulate oncogenic gene expression and that CEBPA-mutated AML is hypersensitive to perturbation of the MLL1 complex. These findings identify the MLL1 complex as a potential therapeutic target in AML with CEBPA mutations.
Keyphrases
- acute myeloid leukemia
- transcription factor
- allogeneic hematopoietic stem cell transplantation
- gene expression
- crispr cas
- induced apoptosis
- dna methylation
- signaling pathway
- genome wide
- end stage renal disease
- endothelial cells
- mental health
- ejection fraction
- poor prognosis
- bone marrow
- climate change
- chronic kidney disease
- dendritic cells
- drug delivery
- oxidative stress
- cell cycle arrest
- copy number
- pi k akt
- drug induced
- wild type
- cell death
- acute lymphoblastic leukemia
- human health
- risk assessment
- peritoneal dialysis
- long non coding rna
- patient reported
- radiofrequency ablation