Evidence map›Paper›PMID 39050859›Full record

ReviewFrontiers in immunology2024

The role of HDAC3 in inflammation: mechanisms and therapeutic implications.

Noah Watson, Sivaraman Kuppuswamy, William Luke Ledford, Sangeetha Sukumari-Ramesh

Abstract readReview
In one paragraph

Review in Frontiers in immunology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing 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

24 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Epigenetic programming of macrophages across inflammatory and malignant diseases.Naunyn-Schmiedeberg's archives of pharmacology · 2026
    Review
  5. Article
  6. Article
  7. Article
  8. Frontiers in pharmacology · 2026
    Review
  9. Article
  10. Review
  11. Review
  12. Review
  13. Review
  14. Review
  15. Histone deacetylases and their inhibitors in kidney diseases.Molecular therapy : the journal of the American Society of Gene Therapy · 2025
    Review
  16. Review
  17. Review
  18. Review
  19. Article
  20. Review
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

4 authors.

Noah WatsonDepartment of Pharmacology and Toxicology, Medical College of Georgia, Augusta University, Augusta, GA, United States.
Sivaraman KuppuswamyDepartment of Pharmacology and Toxicology, Medical College of Georgia, Augusta University, Augusta, GA, United States.
William Luke LedfordDepartment of Pharmacology and Toxicology, Medical College of Georgia, Augusta University, Augusta, GA, United States.
Sangeetha Sukumari-RameshDepartment of Pharmacology and Toxicology, Medical College of Georgia, Augusta University, Augusta, GA, United States.

Funding

HDAC3 as a therapeutic target for intracerebral hemorrhageR01NS132794 · NINDS · AUGUSTA UNIVERSITY · PI Sangeetha Sukumari-Ramesh · 2023 to 2026
$1.6M
The Translocator Protein (TSPO) and Intracerebral HemorrhageR01NS107853 · NINDS · AUGUSTA UNIVERSITY · PI SUKUMARI-RAMESH, SANGEETHA · 2018 to 2021
$1.3M
Quantitative proteomic analysis of the aging brain after intracerebral hemorrhageR03AG077460 · NIA · AUGUSTA UNIVERSITY · PI SUKUMARI-RAMESH, SANGEETHA · 2022 to 2023
$154k
NIA NIH HHS R03 AG077460NINDS NIH HHS R01 NS107853NINDS NIH HHS R01 NS132794
6 · The paper itself

Abstract

Histone deacetylases (HDACs) are critical regulators of inflammatory gene expression, and the efficacy of pan-HDAC inhibitors has been implicated in various disease conditions. However, it remains largely unclear how HDACs precisely regulate inflammation. To this end, evaluating the isoform-specific function of HDACs is critical, and the isoform-specific targeting could also circumvent the off-target effects of pan-HDAC inhibitors. This review provides an overview of the roles of HDAC3, a class I HDAC isoform, in modulating inflammatory responses and discusses the molecular mechanisms by which HDAC3 regulates inflammation associated with brain pathology, arthritis, cardiovascular diseases, lung pathology, allergic conditions, and kidney disorders. The articles also identify knowledge gaps in the field for future studies. Despite some conflicting reports, the selective inhibition of HDAC3 has been demonstrated to play a beneficial role in various inflammatory pathologies. Exploring the potential of HDAC3 inhibition to improve disease prognosis is a promising avenue requiring further investigation.

Indexed as

Histone Deacetylase InhibitorsHistone DeacetylasesInflammationAnimalsHistone Deacetylase 3HumansHistone Deacetylase 3Histone Deacetylase InhibitorsHistone Deacetylasesepigenetic mechanismsHDACHDAC3histone deacetylasesinflammation

Identifiers

PMID39050859
PMCPMC11266039

What OpenQuestion holds

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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.