Evidence map›Paper›PMID 39931769›Full record

ArticleZhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences

Role of EZH2-mediated abnormal histone H3K27me3 methylation in pressure overload-induced cardiac remodeling in mice.

Yixiang Ma, Chang Peng, Shuqi Wu, Xiaochun Tian

Abstract read
In one paragraph

Article in Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. EZH2 promotes malignant biological behavior in esophageal squamous cell carcinoma via EMT.Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences · 2025
    Article
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

4 authors.

Yixiang MaDepartment of Pediatrics, Affiliated Hospital of Zunyi Medical University, Zunyi Guizhou 563000, China. 102323010@qq.com.
Chang PengDepartment of Pediatrics, Affiliated Hospital of Zunyi Medical University, Zunyi Guizhou 563000, China. pengchang_2006@126.com.
Shuqi WuDepartment of Pediatrics, Affiliated Hospital of Zunyi Medical University, Zunyi Guizhou 563000, China.
Xiaochun TianDepartment of Pediatrics, Affiliated Hospital of Zunyi Medical University, Zunyi Guizhou 563000, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesCardiac remodeling is a critical pathological process leading to heart failure. Currently, there is a lack of specific and effective therapies targeting pathological cardiac remodeling. Epigenetics has been shown to play a regulatory role in pathological remodeling. This study aims to explore the impact of inhibiting histone methyltransferase enhancer of zeste homolog 2 (EZH2)-mediated abnormal histone 3 lysine 27 trimethylation (H3K27me3) methylation modification on the progression of pressure overload-induced cardiac remodeling in mice.

methodsMale Kunming mice (specific pathogen-free grade) were randomly divided into groups for 2 experimental parts. Thoracic aortic constriction (TAC) surgery was performed to establish a mouse model of pressure overload-induced cardiac remodeling. In part 1, mice were divided into Normal, Sham, TAC-4W (TAC 4 weeks post-surgery), and TAC-8W (TAC 8 weeks post-surgery) groups. In part 2, mice were divided into Normal, Sham, TAC-8W, TAC+Vehicle (Veh) (TAC with distilled water gavage), and TAC+tanshinone I (Tan I) (TAC with Tan I gavage) groups. Cardiac structure and function were assessed using echocardiography. Histological analysis, Western blotting, and wheat germ agglutinin (WGA) staining was used to evaluate myocardial tissue and cellular changes.

resultsGross examination revealed that the hearts of mice in the TAC-8W group were larger than those in the Sham group, and the hearts in the TAC+Tan I group were further enlarged compared to the TAC-8W group. Echocardiographic analysis showed that, compared to the Sham group, mice in the TAC-4W group exhibited significantly increased left ventricular anterior wall thickness (LVAWT), left ventricular posterior wall thickness (LVPWT), and left ventricular ejection fraction (LVEF), while left ventricular end-diastolic diameter (LVEDD) and left ventricular end-systolic diameter (LVESD) were significantly decreased (all

conclusionsEZH2 inhibition-mediated reduction in H3K27me3 methylation promotes pressure overload-induced cardiac remodeling in mice. EZH2 may serve as a novel therapeutic target for the prevention and treatment of pathological cardiac remodeling.

Indexed as

Enhancer of Zeste Homolog 2 ProteinHistonesVentricular RemodelingAnimalsDisease Models, AnimalHeart FailureMaleMethylationMiceMyocardiumEnhancer of Zeste Homolog 2 ProteinEzh2 protein, mouseHistonesenhancer of zeste homolog 2heart failurehistone 3 lysine 27 trimethylationhistone methylasemethylation modificationmyocardial remodelingtanshinone I

Identifiers

PMID39931769
PMCPMC11814386

What Socratic holds

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LicenceCC BY-NC-ND
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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.