Evidence map›Paper›PMID 34318404›Full record

ReviewCellular oncology (Dordrecht, Netherlands)2021

Histone deacetylase (HDAC) 9: versatile biological functions and emerging roles in human cancer.

Chun Yang, Stéphane Croteau, Pierre Hardy

Open access · hybridAbstract readReview
In one paragraph

Review in Cellular oncology (Dordrecht, Netherlands), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed, 1 pooled it
5.0field-weighted citation impact, top 3% 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

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

  1. Pooled it
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  4. Review
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  7. Review
  8. Article
  9. Localization and quantification of placentalPhysiological genomics · 2025
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  17. Synthesis and biological evaluation ofJournal of enzyme inhibition and medicinal chemistry · 2024
    Article
  18. Epigenetics-targeted drugs: current paradigms and future challenges.Signal transduction and targeted therapy · 2024
    Review
  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

3 authors at 2 institutions in 1 country.

Chun YangResearch Center of CHU Sainte-Justine, University of Montréal, 3175 Côte-Sainte-Catherine, Room 2.17.004, Montréal, Québec, H3T 1C5, Canada.ORCID http://orcid.org/0000-0002-2648-9444
Stéphane CroteauDepartments of Medicine, Pediatrics, Pharmacology and Physiology, University of Montréal, Montréal, QC, Canada.
Pierre HardyResearch Center of CHU Sainte-Justine, University of Montréal, 3175 Côte-Sainte-Catherine, Room 2.17.004, Montréal, Québec, H3T 1C5, Canada. pierre.hardy.med@ssss.gouv.qc.ca.ORCID http://orcid.org/0000-0002-9846-7113
Centre Hospitalier Universitaire Sainte-Justine · CAUniversité de Montréal · CA

Funding

Foundation for the National Institutes of Health 426236
6 · The paper itself

Abstract

backgroundHDAC9 (histone deacetylase 9) belongs to the class IIa family of histone deacetylases. This enzyme can shuttle freely between the nucleus and cytoplasm and promotes tissue-specific transcriptional regulation by interacting with histone and non-histone substrates. HDAC9 plays an essential role in diverse physiological processes including cardiac muscle development, bone formation, adipocyte differentiation and innate immunity. HDAC9 inhibition or activation is therefore a promising avenue for therapeutic intervention in several diseases. HDAC9 overexpression is also common in cancer cells, where HDAC9 alters the expression and activity of numerous relevant proteins involved in carcinogenesis.

conclusionsThis review summarizes the most recent discoveries regarding HDAC9 as a crucial regulator of specific physiological systems and, more importantly, highlights the diverse spectrum of HDAC9-mediated posttranslational modifications and their contributions to cancer pathogenesis. HDAC9 is a potential novel therapeutic target, and the restoration of aberrant expression patterns observed among HDAC9 target genes and their related signaling pathways may provide opportunities to the design of novel anticancer therapeutic strategies.

Indexed as

Gene Expression Regulation, NeoplasticAnimalsCarcinogenesisCell DifferentiationCell NucleusHistone DeacetylasesHistonesHumansNeoplasmsProtein Processing, Post-TranslationalRepressor ProteinsSignal TransductionTranscriptomeHDAC9 protein, humanHistone DeacetylasesHistonesRepressor ProteinsCancer developmentHistone deacetylase (HDAC) 9Myocyte enhancer-binding factor 2-interacting transcriptional repressor (MITR)Signaling pathwaysTumorigenesis

Identifiers

PMID34318404
PMCPMC8516780
OpenAlexW3186586328

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.