Evidence map›Paper›PMID 39419931›Full record

ReviewCell biochemistry and biophysics2025

Histone Deacetylases (HDACs) Roles in Inflammation-mediated Diseases; Current Knowledge.

Saade Abdalkareem Jasim, Farag M A Altalbawy, Mohammad Abohassan, Enwa Felix Oghenemaro, Ashok Kumar Bishoyi, Ravindra Pal Singh, Parjinder Kaur, G V Sivaprasad, Jaafaru Sani Mohammed, Hanen Mahmod Hulail

Abstract readReview
PubMed Publisher
In one paragraph

Review in Cell biochemistry and biophysics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. Article
  2. Review
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  6. Article
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  11. 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

10 authors.

Saade Abdalkareem JasimMedical Laboratory Techniques department, College of Health and Medical Technology, University of Al-maarif, Anbar, Iraq.
Farag M A AltalbawyDepartment of Chemistry, University College of Duba, University of Tabuk, Tabuk, Saudi Arabia. fmaaltalbawy@gmail.com.ORCID http://orcid.org/0000-0003-2708-9159
Mohammad AbohassanDepartment of Clinical Laboratory Sciences, College of Applied Medical Sciences, King Khalid University, Abha, Saudi Arabia.
Enwa Felix OghenemaroDepartment of Pharmaceutical Microbiology, Faculty of Pharmacy, Delta State University, Abraka, Delta State, Nigeria.
Ashok Kumar BishoyiDepartment of Microbiology, Faculty of Science, Marwadi University Research Center, Marwadi University, Rajkot, 360003, Gujarat, India.
Ravindra Pal SinghDepartment of Pharmaceutics, NIMS Institute of Pharmacy, NIMS University Rajasthan, Jaipur, India.
Parjinder KaurChandigarh Pharmacy College, Chandigarh Group of Colleges-Jhanjeri, Mohali, 140307, Punjab, India.
G V SivaprasadDepartment of Basic Science & Humanities, Raghu Engineering College, Visakhapatnam, India.
Jaafaru Sani MohammedMedical Analysis Department, Tishk International University, Erbil, Iraq.
Hanen Mahmod HulailDepartment of Medical Laboratories Technology, AL-Nisour University College, Baghdad, Iraq.

Funding

Deanship of Scientific Research, King Khalid University R.G.P.2/315/44
6 · The paper itself

Abstract

The histone acetyl transferases (HATs) and histone deacetylases (HDACs), which are mostly recognized for their involvement in regulating chromatin remodeling via histone acetylation/deacetylation, have been shown to also change several non-histone proteins to regulate other cellular processes. Acetylation affects the activity or function of cytokine receptors, nuclear hormone receptors, intracellular signaling molecules, and transcription factors in connection to inflammation. Some small-molecule HDAC inhibitors are utilized as anticancer medications in clinical settings due to their capability to regulate cellular growth arrest, differentiation, and death. Here, we summarize our present knowledge of the innate and adaptive immunological pathways that classical HDAC enzymes control. The aim is to justify the targeted (or non-targeted) use of inhibitors against certain HDAC enzymes in inflammatory diseases such as arthritis, inflammatory bowel diseases (IBD), airways inflammation and neurological diseases.

Indexed as

Histone DeacetylasesInflammationAnimalsHistone Deacetylase InhibitorsHumansInflammatory Bowel DiseasesHistone Deacetylase InhibitorsHistone DeacetylasesArthritisHDACsIBDInflammationNeuroinflammation

Identifiers

What Socratic holds

Textmetadata
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.