Evidence map›Paper›PMID 17325655›Full record

ArticleBritish journal of pharmacology2007

HDAC inhibitors as anti-inflammatory agents.

I M Adcock

Registry-linked trialAbstract readComment
In one paragraph

Article in British journal of pharmacology, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02804581 (Potential Role of Gum Arabic as Immunomodulator In Sudanese Rheumatoid Arthritis Patients), which is not on this map. Cited by 112 papers.

0numbers the graph read from it
0cells of the map it votes in
112citing 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.

NCT02804581 phase2unknown statusnot on this mapstarted 2016, after this paper: background citation

Potential Role of Gum Arabic as Immunomodulator In Sudanese Rheumatoid Arthritis Patients

TypeinterventionalSponsorLamis KaddamRan2016 to 2016Enrolled45ConditionsRheumatoid ArthritisArmsGum Arabic
3 · Its place in the literature

Who cites it

112 citing papers in PubMed.

  1. Trial
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  6. Review
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  18. Macrophages and Bone Remodeling.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2023
    Review
  19. Article
  20. Article

52 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

1 author.

I M AdcockAirways Disease Section, National Heart and Lung Institute, Imperial College London, London, UK. ian.adcock@imperial.ac.uk

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Diverse cellular functions including the regulation of inflammatory gene expression, DNA repair and cell proliferation are regulated by changes in the acetylation status of histones and non-histone proteins. Many human diseases, particularly cancer, have been associated with altered patterns of histone acetylation. Furthermore, abnormal expression and activation of histone acetyltransferases, which act as transcriptional co-activators, has been reported in inflammatory diseases. Histone deacetylase (HDAC) inhibitors have been developed clinically for malignancies due to their effects on apoptosis. More recently, in vitro and in vivo data indicates that HDAC inhibitors may be anti-inflammatory due to their effects on cell death acting through acetylation of non-histone proteins. Although there are concerns over the long-term safety of these agents, they may prove useful particularly in situations where current anti-inflammatory therapies are suboptimal.

Indexed as

Histone Deacetylase InhibitorsAnimalsAnti-Inflammatory AgentsHumansInflammationAnti-Inflammatory AgentsHistone Deacetylase Inhibitors

Identifiers

PMID17325655
PMCPMC2013887

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.