Evidence mapPaperPMID 41811528Full record

ReviewInflammation2026

P300 in Inflammation: An Updated Perspective on Its Molecular Mechanisms and Therapeutic Potential.

Ning Zhang, Liang Cao, Dafei Han, Ke Zhou, Zhendong Liao, Jiajia Du, Hongyu Li, Jiajun Zhou, Jianjun Liu, Jiajie Tu

Abstract readReview
In one paragraph

Review in Inflammation, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Ning Zhang *Department of Pharmacy, The Second People's Hospital of Hefei, Hefei Hospital Affiliated to Anhui Medical University246, Heping Road, Yaohai District, Hefei, 230011, Anhui, China.
Liang Cao *Department of Pharmacy, The Second People's Hospital of Hefei, Hefei Hospital Affiliated to Anhui Medical University246, Heping Road, Yaohai District, Hefei, 230011, Anhui, China.
Dafei Han *Key Laboratory of Anti-Inflammatory and Immune Medicine, Ministry of Education, Anhui Collaborative Innovation Center of Anti-Inflammatory and Immune Medicine, Institute of Clinical Pharmacology, Anhui Medical University, 81 Meishan Road, Shushan District, Hefei, China.
Ke ZhouDepartment of Pharmacy, The Second People's Hospital of Hefei, Hefei Hospital Affiliated to Anhui Medical University246, Heping Road, Yaohai District, Hefei, 230011, Anhui, China.
Zhendong LiaoDepartment of Pharmacy, The Second People's Hospital of Hefei, Hefei Hospital Affiliated to Anhui Medical University246, Heping Road, Yaohai District, Hefei, 230011, Anhui, China.
Jiajia DuDepartment of Pharmacy, The Second People's Hospital of Hefei, Hefei Hospital Affiliated to Anhui Medical University246, Heping Road, Yaohai District, Hefei, 230011, Anhui, China.
Hongyu LiDepartment of Pharmacy, The Second People's Hospital of Hefei, Hefei Hospital Affiliated to Anhui Medical University246, Heping Road, Yaohai District, Hefei, 230011, Anhui, China.
Jiajun ZhouDepartment of Pharmacy, The Second People's Hospital of Hefei, Hefei Hospital Affiliated to Anhui Medical University246, Heping Road, Yaohai District, Hefei, 230011, Anhui, China.
Jianjun LiuDepartment of Pharmacy, The Second People's Hospital of Hefei, Hefei Hospital Affiliated to Anhui Medical University246, Heping Road, Yaohai District, Hefei, 230011, Anhui, China. LJJhfSPH@outlook.com.
Jiajie TuKey Laboratory of Anti-Inflammatory and Immune Medicine, Ministry of Education, Anhui Collaborative Innovation Center of Anti-Inflammatory and Immune Medicine, Institute of Clinical Pharmacology, Anhui Medical University, 81 Meishan Road, Shushan District, Hefei, China. tujiajie@ahmu.edu.cn.

Funding

National Natural Science Foundation of China 82373877Research Project of Distinguished Youth of University in Anhui Province 2022AH020052
6 · The paper itself

Abstract

Transcription cofactor p300 is characterized by histone acetyltransferase (HAT) activity, which endows p300 with dual functions of chromatin remodeling and gene transcription and participates in regulating various basic cellular functions. P300 mainly enhances the expression of downstream pro-inflammatory factors such as TNF-α and IL-6 by acetylating core transcription factors in the inflammatory signaling pathway, such as NF-κB and JAK/STAT. P300 also reshapes the epigenetic profile of important cellular components in inflammation, such as macrophages or T cells, by mediating histone H3K27ac modification. Based on the above molecular mechanisms, p300 plays a key role in various inflammatory diseases, including respiratory inflammatory, autoimmune, metabolic-related and neuroinflammatory diseases as well as infectious inflammation. Small molecule inhibitors targeting p300 show anti-inflammatory potential in various preclinical animal models; however, their tissue-specific targeting mechanisms and long-term safety need further exploration. The current review summarizes the molecular mechanism basis, cell specific functions, and targeted intervention strategies of p300 in inflammatory diseases, and explores the development of novel p300-based anti-inflammatory medication.

Indexed as

E1A-Associated p300 ProteinInflammationp300-CBP Transcription FactorsAnimalsAnti-Inflammatory AgentsHumansSignal TransductionAnti-Inflammatory AgentsE1A-Associated p300 ProteinEP300 protein, humanp300-CBP Transcription FactorsHIF-1αInflammationMacrophage; T cellNF-κBP300

Identifiers

PMID41811528
PMCPMC13009107

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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.