A novel murine model of myeloproliferative disorders generated by overexpression of the transcription factor NF-E2

Kai B Kaufmann1, Albert Gründer, Tobias Hadlich

  • 1Department of Experimental Anaesthesiology, Center for Clinical Research, University Hospital Freiburg, Germany.

Insights

Overexpressed NF-E2 drives myeloproliferative neoplasms (MPNs) in mice, mimicking human disease. Histone deacetylase inhibitors (HDAC-Is) reversed MPN features by reducing NF-E2, suggesting epigenetic therapy potential.

Area of Science:

  • Hematology
  • Molecular Biology
  • Oncology

Background:

  • The molecular basis of myeloproliferative neoplasms (MPNs) is not fully understood.
  • NF-E2 transcription factor overexpression is observed in MPN patients.

Purpose of the Study:

  • To investigate the role of NF-E2 in MPN pathogenesis.
  • To explore epigenetic modifications as therapeutic targets in MPNs.

Main Methods:

  • Generated mice with NF-E2 transgene in hematopoietic cells to model MPNs.
  • Utilized histone deacetylase inhibitor (HDAC-I) vorinostat for treatment.
  • Analyzed histone modifications and NF-E2 expression levels.

Main Results:

  • NF-E2 transgenic mice displayed MPN features including thrombocytosis, leukocytosis, and transformation to acute myeloid leukemia.
  • NF-E2 overexpression led to histone H3 hypoacetylation.
  • Vorinostat treatment normalized platelet counts and reduced NF-E2 expression in mice.
  • MPN patients treated with HDAC-I also showed decreased NF-E2 expression.

Conclusions:

  • NF-E2 plays a crucial role in the pathophysiology of MPNs.
  • Epigenetic alterations, specifically histone acetylation, are implicated in MPN development.
  • HDAC inhibitors represent a promising therapeutic strategy for MPNs targeting NF-E2.

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