Evidence map›Paper›PMID 33117806›Full record

ReviewFrontiers in cell and developmental biology2020

Histone Deacetylases and Histone Deacetylase Inhibitors in Neuroblastoma.

Monica Phimmachanh, Jeremy Z R Han, Yolande E I O'Donnell, Sharissa L Latham, David R Croucher

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in cell and developmental biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
2.3field-weighted citation impact, top 11% 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

33 citing papers in PubMed, 54 citations in OpenAlex.

  1. Review
  2. Article
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  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. MS275 Inhibits Neuroblastoma Cell Growth by Mediating H3K27ac/PROX1 Axis In Silico and In Vitro.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2025
    Article
  15. Review
  16. Review
  17. Article
  18. BML-281 promotes neuronal differentiation by modulating Wnt/CaMolecular and cellular biochemistry · 2024
    Article
  19. Article
  20. Histone Deacetylases in Retinoblastoma.International journal of molecular sciences · 2024
    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

5 authors at 3 institutions in 1 country.

Monica PhimmachanhThe Kinghorn Cancer Centre, Garvan Institute of Medical Research, Sydney, NSW, Australia.
Jeremy Z R HanThe Kinghorn Cancer Centre, Garvan Institute of Medical Research, Sydney, NSW, Australia.
Yolande E I O'DonnellThe Kinghorn Cancer Centre, Garvan Institute of Medical Research, Sydney, NSW, Australia.
Sharissa L LathamThe Kinghorn Cancer Centre, Garvan Institute of Medical Research, Sydney, NSW, Australia.
David R CroucherThe Kinghorn Cancer Centre, Garvan Institute of Medical Research, Sydney, NSW, Australia.
Garvan Institute of Medical Research · AUSt Vincent's Hospital · AUThe Kinghorn Cancer Centre · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Histone deacetylases (HDACs) are enzymes that play a key role in regulating gene expression by remodeling chromatin structure. An imbalance of histone acetylation caused by deregulated HDAC expression and activity is known to promote tumor progression in a number of tumor types, including neuroblastoma, the most common solid tumor in children. Consequently, the inhibition of HDACs has emerged as a potential strategy to reverse these aberrant epigenetic changes, and several classes of HDAC inhibitors (HDACi) have been shown to inhibit tumor proliferation, or induce differentiation, apoptosis and cell cycle arrest in neuroblastoma. Further, the combined use of HDACi with other chemotherapy agents, or radiotherapy, has shown promising pre-clinical results and various HDACi have progressed to different stages in clinical trials. Despite this, the effects of HDACi are multifaceted and more work needs to be done to unravel their specific mechanisms of actions. In this review, we discuss the functional role of HDACs in neuroblastoma and the potential of HDACi to be optimized for development and use in the clinic for treatment of patients with neuroblastoma.

Indexed as

acetylationapoptosiscell cycle arrestdifferentiationhistone deacetylase inhibitorhistone deacetylasesneuroblastoma

Identifiers

PMID33117806
PMCPMC7575710
OpenAlexW3092441903

What OpenQuestion 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 OpenQuestion graph.