Evidence map›Paper›PMID 35303381›Full record

ReviewThe FEBS journal2023

Histone deacetylase 7: a signalling hub controlling development, inflammation, metabolism and disease.

Yizhuo Wang, Rishika Abrol, Jeffrey Y W Mak, Kaustav Das Gupta, Divya Ramnath, Denuja Karunakaran, David P Fairlie, Matthew J Sweet

Open access · hybridAbstract readReview
In one paragraph

Review in The FEBS journal, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed, 1 pooled it
7.3field-weighted citation impact, top 2% 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

43 citing papers in PubMed, 1 synthesis or guideline pooled it, 71 citations in OpenAlex.

  1. Pooled it
  2. STAT1: a central hub linking ferroptosis and inflammation in hepatic ischemia-reperfusion injury.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2026
    Review
  3. Review
  4. Harnessing Substituted 4-Chlorothieno[2,3-Pharmaceuticals (Basel, Switzerland) · 2026
    Article
  5. Article
  6. Article
  7. Article
  8. Photoperiod-driven gene regulation in the brain ofFrontiers in endocrinology · 2026
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Review
  18. Article
  19. Article
  20. 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

8 authors at 1 institution in 1 country.

Yizhuo WangInstitute for Molecular Bioscience (IMB), The University of Queensland, St. Lucia, Australia.
Rishika AbrolInstitute for Molecular Bioscience (IMB), The University of Queensland, St. Lucia, Australia.
Jeffrey Y W MakInstitute for Molecular Bioscience (IMB), The University of Queensland, St. Lucia, Australia.
Kaustav Das GuptaInstitute for Molecular Bioscience (IMB), The University of Queensland, St. Lucia, Australia.
Divya RamnathInstitute for Molecular Bioscience (IMB), The University of Queensland, St. Lucia, Australia.
Denuja KarunakaranInstitute for Molecular Bioscience (IMB), The University of Queensland, St. Lucia, Australia.
David P FairlieInstitute for Molecular Bioscience (IMB), The University of Queensland, St. Lucia, Australia.
Matthew J SweetInstitute for Molecular Bioscience (IMB), The University of Queensland, St. Lucia, Australia.ORCID 0000-0002-0406-8139
The University of Queensland · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Histone deacetylases (HDACs) catalyse removal of acetyl groups from lysine residues on both histone and non-histone proteins to control numerous cellular processes. Of the 11 zinc-dependent classical HDACs, HDAC4, 5, 7 and 9 are class IIa HDAC enzymes that regulate cellular and developmental processes through both enzymatic and non-enzymatic mechanisms. Over the last two decades, HDAC7 has been associated with key roles in numerous physiological and pathological processes. Molecular, cellular, in vivo and disease association studies have revealed that HDAC7 acts through multiple mechanisms to control biological processes in immune cells, osteoclasts, muscle, the endothelium and epithelium. This HDAC protein regulates gene expression, cell proliferation, cell differentiation and cell survival and consequently controls development, angiogenesis, immune functions, inflammation and metabolism. This review focuses on the cell biology of HDAC7, including the regulation of its cellular localisation and molecular mechanisms of action, as well as its associative and causal links with cancer and inflammatory, metabolic and fibrotic diseases. We also review the development status of small molecule inhibitors targeting HDAC7 and their potential for intervention in different disease contexts.

Indexed as

Histone DeacetylasesNeoplasmsHistone Deacetylase InhibitorsHumansInflammationSignal TransductionHistone Deacetylase InhibitorsHistone Deacetylasesclass IIa HDACgene regulationHDAC7immunometabolismmacrophage

Identifiers

PMID35303381
PMCPMC10952174
OpenAlexW4221116152

What Socratic holds

Textmetadata
LicenceCC BY
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.