Evidence map›Paper›PMID 40717095›Full record

ArticleScientific reports2025

Identification of a key smooth muscle cell subset driving ischemic cardiomyopathy progression through single-cell RNA sequencing.

Wenyang Nie, Yong Wang, Yuanyuan Xiao, Zhiheng Lin, Jingwen Zhang, Zhijie Zhao, Zhen Wang

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Article
  3. 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

7 authors.

Wenyang Nie *First Clinical Medical College, Shandong University of Traditional Chinese Medicine, 16369 Jingshi Rd, Jinan, 250014, China.ORCID http://orcid.org/0009-0009-4688-6402
Yong Wang *Department of Cardiovascular Diseases, Affiliated Hospital of Shandong University of Traditional Chinese Medicine, 16369 Jingshi Rd, Jinan, 250014, China.ORCID http://orcid.org/0000-0001-7428-8754
Yuanyuan Xiao *Department of Ophthalmology, Shanghai University of Medicine & Health Sciences Affiliated Zhoupu Hospital, 1500 Zhouyuan Rd, Shanghai, 201318, China.
Zhiheng LinDepartment of Gynecology, Longhua Hospital, Shanghai University of Traditional Chinese Medicine, Shanghai, 200032, China.
Jingwen ZhangDepartment of Cardiovascular Diseases, Affiliated Hospital of Shandong University of Traditional Chinese Medicine, 16369 Jingshi Rd, Jinan, 250014, China.
Zhijie ZhaoDepartment of Plastic and Reconstructive Surgery, Shanghai Ninth People's Hospital, School of Medicine, Shanghai Jiao Tong University, 639 Zhi Zao Ju Rd, Shanghai, 200011, China. zhaozhijie@sjtu.edu.cn.ORCID http://orcid.org/0000-0001-5587-8855
Zhen WangDepartment of Cardiovascular Diseases, Affiliated Hospital of Shandong University of Traditional Chinese Medicine, 16369 Jingshi Rd, Jinan, 250014, China. 71000799@sdutcm.edu.cn.ORCID http://orcid.org/0009-0002-8554-4121

Funding

Jinan Science and Technology Plan Project 202225004Natural Science Foundation of Shandong Province general project ZR2022MH307Young Scientists Fund of the National Natural Science Foundation of China No. 82104797
6 · The paper itself

Abstract

Cardiomyopathy encompasses a range of diseases that severely affect the complex functions of the heart, involving structural and functional abnormalities, and is associated with high mortality. Recent studies have highlighted the critical role of ferroptosis in regulating oxidative stress and inflammation in cardiomyopathy. In this study, we established that the C6 S100A4+ SMCs subpopulation is critical by performing an integrated single-cell analysis of the known publicly available data GSE145154. We validated the role of S100A4 in SMCs through in vitro experiments, providing evidence for its potential as a therapeutic target. Furthermore, these cells interact with endothelial cells through the PTN-NCL pathway, influencing disease progression. Key transcription factors, including KLF2, FOS, FOSB, and JUNB, were identified. This key subpopulation, along with its associated signaling pathways, marker genes, stemness genes, and transcription factors, may offer new insights for preventing the onset and progression of cardiomyopathy, particularly ischemic cardiomyopathy.

Indexed as

CardiomyopathiesMyocardial IschemiaMyocytes, Smooth MuscleSingle-Cell AnalysisAnimalsDisease ProgressionEndothelial CellsHumansRatsSequence Analysis, RNASignal TransductionCardiomyopathyExosomesFerroptosisInflammationSingle-cell RNA sequencingSmooth muscle cells

Identifiers

PMID40717095
PMCPMC12301475

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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.