Evidence mapPaperPMID 42435177Full record

ReviewAdvances in experimental medicine and biology2026

Epigenetic Targeting in Myeloid Malignancies.

Bruno António Cardoso

Abstract readReview
PubMed Publisher
In one paragraph

Review in Advances in experimental medicine and biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

1 author.

Bruno António CardosoUniversidade Católica Portuguesa, Faculdade de Medicina, Sintra, Portugal. bacardoso@ucp.pt.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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.

Indexed as

Antineoplastic AgentsEpigenesis, GeneticAnimalsDNA MethylationHistone Deacetylase InhibitorsHistonesHumansMolecular Targeted TherapyAntineoplastic AgentsHistone Deacetylase InhibitorsHistonesDNA methylationEpigenetic therapyHistone modificationsMyeloid malignancies

Identifiers

What Socratic holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.