Evidence map›Paper›PMID 39963253›Full record

ReviewTherapeutic advances in gastroenterology2025

Histone deacetylase in inflammatory bowel disease: novel insights.

Chunxiao Li, Shaobo Gu, Yihong Zhang, Zhenruo Zhang, Junzhuo Wang, Ting Gao, Kangpeng Zhong, Keshu Shan, Guoliang Ye, Yini Ke and 1 more

Abstract readReview
In one paragraph

Review in Therapeutic advances in gastroenterology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Article
  5. 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

11 authors.

Chunxiao LiDepartment of Gastroenterology, The First Affiliated Hospital of Ningbo University, Ningbo, Zhejiang, China.ORCID https://orcid.org/0000-0003-2433-2408
Shaobo GuDepartment of Orthopedics, Ningbo No. 2 Hospital, Ningbo, Zhejiang, China.ORCID https://orcid.org/0009-0006-7492-6342
Yihong ZhangDepartment of Gastroenterology, The First Affiliated Hospital, College of Medicine, Zhejiang University, Hangzhou, Zhejiang, China.
Zhenruo ZhangArrhythmia Center, The First Affiliated Hospital of Ningbo University, Ningbo, Zhejiang, China.
Junzhuo WangDepartment of Gastroenterology, The First Affiliated Hospital of Ningbo University, Ningbo, Zhejiang, China.
Ting GaoDepartment of Gastroenterology, The First Affiliated Hospital of Ningbo University, Ningbo, Zhejiang, China.
Kangpeng ZhongDepartment of Gastroenterology, The First Affiliated Hospital of Ningbo University, Ningbo, Zhejiang, China.
Keshu ShanDepartment of Gastroenterology, The First Affiliated Hospital of Ningbo University, Ningbo, Zhejiang, China.
Guoliang YeDepartment of Gastroenterology, The First Affiliated Hospital of Ningbo University, Ningbo, Zhejiang, China.
Yini KeDepartment of Rheumatology, The First Affiliated Hospital, College of Medicine, Zhejiang University, Hangzhou, Zhejiang, China.
Yi ChenDepartment of Gastroenterology, The First Affiliated Hospital, College of Medicine, Zhejiang University, 79 Qingchun Road, Hangzhou 310003, China.ORCID https://orcid.org/0000-0002-5216-6972

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Inflammatory bowel disease (IBD), including ulcerative colitis and Crohn's disease, is characterized by chronic nonspecific intestinal inflammation. Despite considerable efforts, IBD remains a heavy burden on society and human health, with increasing morbidity. Posttranslational modification, especially histone acetylation, is a key process in controlling DNA transcriptional activity. Histone deacetylases (HDACs) play a vital role in the mechanism of IBD pathogenesis through histone and nonhistone protein deacetylation. Herein, we present a summary of different categories of HDACs as well as HDAC inhibitors (HDACis) and analyze the role of HDAC inhibition in alleviating IBD along with its mechanism, as well as clinical potential of HDACis in IBD treatment.

Indexed as

HDAC inhibitors (HDACis)histone deacetylases (HDACs)inflammatory bowel disease (IBD)T cell function

Identifiers

PMID39963253
PMCPMC11831641

What Socratic holds

Textmetadata
LicenceCC BY-NC
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.