Evidence map›Paper›PMID 42756899›Full record

ReviewFrontiers in molecular neuroscience2026

KAT5: the epigenetic regulator of central nervous system diseases.

Xiaoming Xin, Lingjuan Wu, Meichen Liu, Tian Liu, Zihan Yuan, Liang Zhang, Tongqing Duan, Lei Zhang, Xianmin Zhu

Abstract readReview
In one paragraph

Review in Frontiers in molecular neuroscience, 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

9 authors.

Xiaoming Xin *Shanghai University of Medicine and Health Sciences, Shanghai, China.
Lingjuan Wu *Shanghai University of Traditional Chinese Medicine, Shanghai, China.
Meichen LiuShanghai University of Medicine and Health Sciences, Shanghai, China.
Tian LiuShanghai University of Medicine and Health Sciences, Shanghai, China.
Zihan YuanShanghai University of Medicine and Health Sciences, Shanghai, China.
Liang ZhangQingdao Eighth People's Hospital, Qingdao, China.
Tongqing DuanQingdao Cardiovascular Disease Hospital, Qingdao, China.
Lei ZhangJinshan Central Hospital Affiliated to Shanghai University of Medicine and Health Sciences, Shanghai, China.
Xianmin ZhuShanghai Academy of Sciences and Technology Institute of Model Animals Transformation, Shanghai, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Abnormal epigenetic modifications are involved in central nervous system (CNS) diseases. Histones play a crucial role in chromatin structure and function, whose post-translational modifications significantly impact gene expression and chromatin dynamics. Histone acetylation, governed by the balance between histone acetyltransferases (HATs) and histone deacetylases (HDACs), is one of the key modulators of chromatin accessibility and transcriptional activity. Lysine acetyltransferase 5 (KAT5, aka TIP60), a member of the MYST subfamily of HATs, is involved in many cellular processes, including DNA repair, apoptosis, and cell cycle control. Notably, the dysfunction of KAT5 has been implicated in several CNS diseases. In this review, we explored the roles of KAT5 in CNS pathophysiology, emphasizing its involvement in neurological disorders and its potential as a therapeutic target. This review sheds light on the epigenetic mechanisms in CNS diseases mediated by KAT5 and provides valuable information for potential treatment strategies.

Indexed as

acetylationCNS diseasesepigenetic modificationhistonesKAT5

Identifiers

PMID42756899
PMCPMC13583670

What OpenQuestion 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 OpenQuestion graph.