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Proliferation and Differentiation of Murine Myeloid Precursor 32D/G-CSF-R Cells
Published on: February 21, 2018
Epigenetic Targeting in Myeloid Malignancies
1Universidade Católica Portuguesa, Faculdade de Medicina, Sintra, Portugal. bacardoso@ucp.pt.
Abstract:
Epigenetic deregulation is a hallmark of myeloid malignancies, shaping their initiation, progression, and therapeutic response. Unlike genetic alterations, epigenetic modifications, such as DNA methylation, histone acetylation, and chromatin remodeling, are reversible, making them attractive targets for pharmacological intervention. This chapter aims to provide a detailed and comprehensive overview of epigenetic drugs currently available in both preclinical and clinical testing, with a particular focus on agents directed against histone deacetylases (HDACs), DNA methyltransferases (DNMTs), histone methyltransferases (HMTs), histone demethylases (HDMs), bromodomain and extra-terminal (BET) proteins, and mutant IDH1/2 enzymes. By detailing the mechanisms of action and the available translational data for these pharmacological agents, the chapter aims to summarize the current state of epigenetic therapy and highlight how the development of epigenetic therapies is shaping the clinical landscape of myeloid malignancies.
Insights
Epigenetic drugs targeting DNA methylation and histone modifications offer reversible treatments for myeloid malignancies. These therapies are advancing the clinical landscape for these cancers.
Area of Science:
- Oncology
- Pharmacology
- Epigenetics
Background:
- Epigenetic deregulation is a key feature in myeloid malignancies, influencing disease development and treatment outcomes.
- Epigenetic modifications are reversible, presenting unique opportunities for targeted drug development.
Purpose of the Study:
- To provide a comprehensive overview of current epigenetic drugs in preclinical and clinical development for myeloid malignancies.
- To detail the mechanisms of action and translational data for key epigenetic drug classes.
Main Methods:
- Review of preclinical and clinical data for epigenetic drugs.
- Focus on agents targeting histone deacetylases (HDACs), DNA methyltransferases (DNMTs), histone methyltransferases (HMTs), histone demethylases (HDMs), BET proteins, and mutant IDH1/2 enzymes.
Main Results:
- Summary of the current landscape of epigenetic therapies for myeloid malignancies.
- Highlighting the translational progress and clinical impact of these agents.
Conclusions:
- Epigenetic therapies are a rapidly evolving area in treating myeloid malignancies.
- These reversible treatments are significantly reshaping the clinical management of these hematological cancers.
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