MECOM is a master repressor of myeloid differentiation through dose control of <i>CEBPA</i> in acute myeloid leukemia

The transcription factor MECOM, located at 3q26, is essential for hematopoietic stem cells in healthy individuals. Enhancer translocations, due to 3q26 rearrangements, drive out-of-context MECOM expression in one of the most aggressive subtypes of acute myeloid leukemia (AML). Aberrantly expressed MECOM is essential for the survival and immature phenotype of these leukemia cells. Direct depletion of MECOM using an endogenous auxin-inducible degron immediately upregulates expression of CEBPA, which encodes a transcription factor required for neutrophil development and is frequently mutated in other AML subtypes. MECOM depletion is accompanied by a severe loss of CD34 and gain of mature myeloid cell surface marker CD15. MECOM exerts its inhibitory effect on differentiation by binding to the +42-kilobase CEBPA enhancer. This is partially dependent on the interaction between MECOM and its corepressor CTBP2. We demonstrate that CEBPA overexpression can bypass the MECOM-mediated block of differentiation. In addition, patients with AML with MECOM overexpression through enhancer hijacking show significantly reduced CEBPA levels. Our study directly connects 2 major players in normal and malignant hematopoiesis, MECOM and CEBPA, and unveils how MECOM maintains self-renewal by repressing CEBPA-induced differentiation.

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Journal
Blood
Published
2025-10-08
DOI
https://doi.org/10.1182/blood.2025028914
Citations
5
Primary Topic
Acute Myeloid Leukemia Research
Type
article
Field-Weighted Citation Impact
8.85
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article

MECOM is a master repressor of myeloid differentiation through dose control of CEBPA in acute myeloid leukemia

Julie A.I. Thoms, Sophie Ottema, Marije Havermans, Claudia Erpelinck-Verschueren et al.
5 citations
Blood
Acute Myeloid Leukemia Research
8.85
article

MECOM is a master repressor of myeloid differentiation through dose control of CEBPA in acute myeloid leukemia

Julie A.I. Thoms, Sophie Ottema, Marije Havermans, Claudia Erpelinck-Verschueren, Maikel Anthonissen, Eric Bindels, Torsten Haferlach, Stanley van Herk, Bas J. Wouters, John E. Pimanda, Claudia Haferlach, Ruud Delwel, Roger Mulet‐Lazaro, H. Berna Beverloo, Dorien Pastoors, Leonie Smeenk, Johannes Zuber, Tim Grob, Shruthi Subramanian
article en
5 citations

Abstract

The transcription factor MECOM, located at 3q26, is essential for hematopoietic stem cells in healthy individuals. Enhancer translocations, due to 3q26 rearrangements, drive out-of-context MECOM expression in one of the most aggressive subtypes of acute myeloid leukemia (AML). Aberrantly expressed MECOM is essential for the survival and immature phenotype of these leukemia cells. Direct depletion of MECOM using an endogenous auxin-inducible degron immediately upregulates expression of CEBPA, which encodes a transcription factor required for neutrophil development and is frequently mutated in other AML subtypes. MECOM depletion is accompanied by a severe loss of CD34 and gain of mature myeloid cell surface marker CD15. MECOM exerts its inhibitory effect on differentiation by binding to the +42-kilobase CEBPA enhancer. This is partially dependent on the interaction between MECOM and its corepressor CTBP2. We demonstrate that CEBPA overexpression can bypass the MECOM-mediated block of differentiation. In addition, patients with AML with MECOM overexpression through enhancer hijacking show significantly reduced CEBPA levels. Our study directly connects 2 major players in normal and malignant hematopoiesis, MECOM and CEBPA, and unveils how MECOM maintains self-renewal by repressing CEBPA-induced differentiation.

BloodVol. 146(25)
The University of Sydney (AU), Oregon Health & Science University (US), Research Institute of Molecular Pathology (AT), Erasmus MC (NL), UNSW Sydney (AU), Munich Leukemia Laboratory (Germany) (DE), Prince of Wales Hospital (AU), Oncode Institute (NL), Vienna Biocenter (AT), Erasmus MC Cancer Institute (NL), Rotterdam University of Applied Sciences (NL), Erasmus University Rotterdam (NL)
Openalex Percentile: Top 2%
Acute Myeloid Leukemia Research
8.85
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