Evidence map›Paper›PMID 36350520›Full record

ReviewAdvances in experimental medicine and biology2022

Inhibitors of DNA Methylation.

Marie Lopez, Julie Gilbert, Jean Contreras, Ludovic Halby, Paola B Arimondo

Abstract readReview
PubMed Publisher
In one paragraph

Review in Advances in experimental medicine and biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
12.0field-weighted citation impact, top 1% of its field
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

14 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Spinal Cord Injury Remyelination: Pathways to Therapies.International journal of molecular sciences · 2025
    Review
  5. Article
  6. Review
  7. Review
  8. Review
  9. Article
  10. Review
  11. Review
  12. Clinical applications of abnormal DNA methylation in chronic myeloid leukemia.Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences · 2024
    Article
  13. Article
  14. Article
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

5 authors at 3 institutions in 1 country.

Marie LopezInstitut des Biomolécules Max Mousseron (IBMM), CNRS, Université de Montpellier, ENSCM UMR 5247, Montpellier, France.
Julie GilbertInstitut des Biomolécules Max Mousseron (IBMM), CNRS, Université de Montpellier, ENSCM UMR 5247, Montpellier, France.
Jean ContrerasEpigenetic Chemical Biology, Department of Structural Biology and Chemistry, Institut Pasteur, Université de Paris, CNRS UMR3523 Chem4Life, Paris, France.
Ludovic HalbyEpigenetic Chemical Biology, Department of Structural Biology and Chemistry, Institut Pasteur, Université de Paris, CNRS UMR3523 Chem4Life, Paris, France.
Paola B ArimondoEpigenetic Chemical Biology, Department of Structural Biology and Chemistry, Institut Pasteur, Université de Paris, CNRS UMR3523 Chem4Life, Paris, France. paola.arimondo@cnrs.fr.
Centre National de la Recherche Scientifique · FRInstitut des Biomolécules Max Mousseron · FRUniversité Paris Cité · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

DNA methylation is involved in numerous biological processes and is deregulated in human diseases. The modulation of the activity of the enzymes and proteins in charge of DNA methylation, for example, DNA methyltransferases (DNMTs), can represent a powerful strategy to alter DNA methylation patterns and restore biological processes that are aberrant in diseases. In this chapter, we present examples of inhibitors of DNMTs (DNMTi). We review their fields of application either as therapeutic molecules, for example, in cancers, cardiovascular, neurological, and infectious diseases or as bioengineering tools. Finally, novel strategies to target DNA methylation and overcome the limits of single DNMT inhibitors will be described. These strategies consist in either targeting the methyl group reader proteins rather than targeting directly DNMTs or to combine within the same molecule a DNMT inhibitor with an additional active moiety, e.g., HDAC inhibitor, to improve efficacy and lower secondary effect of such drug.

Indexed as

DNA MethylationNeoplasmsDNA (Cytosine-5-)-MethyltransferasesDNA Modification MethylasesEnzyme InhibitorsHistone Deacetylase InhibitorsHumansDNA (Cytosine-5-)-MethyltransferasesDNA Modification MethylasesEnzyme InhibitorsHistone Deacetylase InhibitorsAchemical biologyDNA methyltransferasesDNMT inhibitorsMBDMethylbinding proteinstherapeutic strategies

Identifiers

PMID36350520
OpenAlexW4308770722

What OpenQuestion 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 OpenQuestion graph.