Evidence map›Paper›PMID 40969373›Full record

ReviewFrontiers in endocrinology2025

The role of protein S-acylation in vascular injury associated with metabolic disorders.

Yayun Wang, Wenhui Zhu, Wenfan Wang, Jiayi Zhang, Dongsen Hu, Huanmeng Shao, Yingtong Zhou, Shan Wang, Linhua Zhao

Erratum issuedAbstract readReview
In one paragraph

Review in Frontiers in endocrinology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors.

Yayun Wang *The Affiliated Hospital to Changchun University of Chinese Medicine, Changchun, Jilin, China.
Wenhui Zhu *The Affiliated Hospital to Changchun University of Chinese Medicine, Changchun, Jilin, China.
Wenfan Wang *The Affiliated Hospital to Changchun University of Chinese Medicine, Changchun, Jilin, China.
Jiayi ZhangThe Affiliated Hospital to Changchun University of Chinese Medicine, Changchun, Jilin, China.
Dongsen HuBeijing University of Chinese Medicine, Beijing, China.
Huanmeng ShaoBinzhou Medical University, Yantai, Shandong, China.
Yingtong ZhouBinzhou Medical University, Yantai, Shandong, China.
Shan WangNational Center for Integrative Medicine, China Japan Friendship Hospital, Beijing, China.
Linhua ZhaoThe Affiliated Hospital to Changchun University of Chinese Medicine, Changchun, Jilin, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Protein palmitoylation represents a prevalent form post-translational lipid modification across various organisms. This reversible and dynamic cellular process is significant in regulating the transcription and expression of downstream target genes, as well as in facilitating signal transduction. Consequently, it affects various cellular activities, including innate immunity, inflammation, glucose metabolism, lipid metabolism, and functions of the brain and heart. Vascular injury emerges as a critical target organ affected by complications associated with metabolic diseases, and the palmitoylation modifications are implicated in numerous pathological processes. This review offers an overview of current understanding on protein palmitoylation and palmitic acid, emphasizing the influence of the palmitoylation modification on cellular signal transduction in metabolic diseases and exploring its connection with metabolism-related conditions such as diabetic cardiopathy, diabetic nephropathy, and fatty liver diseases. Palmitoleic acid modification holds great promise for tackling challenges related to drug specificity, off-target effects, and delivery mechanisms in the exploration of targeted palmitoleic acid modification therapy

Indexed as

LipoylationMetabolic DiseasesProtein Processing, Post-TranslationalVascular System InjuriesAcylationAnimalsHumansSignal Transductiondiabetes mellitusmetabolic disorderspalmitic acidprotein palmitoylationvascular injury

Identifiers

PMID40969373
PMCPMC12440770

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.