Evidence map›Paper›PMID 35111821›Full record

ArticleFrontiers in cardiovascular medicine2021

Blockade of the Notch Signaling Pathway Promotes M2 Macrophage Polarization to Suppress Cardiac Fibrosis Remodeling in Mice With Myocardial Infarction.

Zhi Li, Miao Nie, Liming Yu, Dengshun Tao, Qiang Wang, Yuanchen He, Yu Liu, Yuji Zhang, Hongguang Han, Huishan Wang

Open access · goldAbstract read
In one paragraph

Article in Frontiers in cardiovascular medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
4.6field-weighted citation impact, top 4% of its field
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

23 citing papers in PubMed, 31 citations in OpenAlex.

  1. Review
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  5. Characterizing the pan-cancer role of exosomal miRNAs in metastasis across cancers.Computational and structural biotechnology journal · 2025
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  13. Characterizing the role of exosomal miRNAs in metastasis.bioRxiv : the preprint server for biology · 2024
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  17. Interleukin-13 contributes to the occurrence of oral submucosal fibrosis.Journal of cellular and molecular medicine · 2023
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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 at 2 institutions in 1 country.

Zhi LiDepartment of Cardiothoracic Surgery, General Hospital of Northern Theater Command, Shenyang, China.
Miao NieCollege of Animal Science and Veterinary Medicine, Shenyang Agricultural University, Shenyang, China.
Liming YuDepartment of Cardiothoracic Surgery, General Hospital of Northern Theater Command, Shenyang, China.
Dengshun TaoDepartment of Cardiothoracic Surgery, General Hospital of Northern Theater Command, Shenyang, China.
Qiang WangDepartment of Cardiothoracic Surgery, General Hospital of Northern Theater Command, Shenyang, China.
Yuanchen HeDepartment of Cardiothoracic Surgery, General Hospital of Northern Theater Command, Shenyang, China.
Yu LiuDepartment of Cardiothoracic Surgery, General Hospital of Northern Theater Command, Shenyang, China.
Yuji ZhangDepartment of Cardiothoracic Surgery, General Hospital of Northern Theater Command, Shenyang, China.
Hongguang HanDepartment of Cardiothoracic Surgery, General Hospital of Northern Theater Command, Shenyang, China.
Huishan WangDepartment of Cardiothoracic Surgery, General Hospital of Northern Theater Command, Shenyang, China.
General Hospital of Shenyang Military Region · CNShenyang Agricultural University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Myocardial infarction (MI) is regarded as a serious ischemic heart disease on a global level. The current study set out to explore the mechanism of the Notch signaling pathway in the regulation of fibrosis remodeling after the occurrence of MI. First, experimental mice were infected with recombination signal binding protein J (RBP-J) shRNA and empty adenovirus vector, followed by the establishment of MI mouse models and detection of cardiac function. After 4 weeks of MI, mice in the sh-RBP-J group were found to exhibit significantly improved cardiac function relative to the sh-NC group. Moreover, knockdown of RBP-J brought about decreased infarct area, promoted cardiac macrophages M2 polarization, reduced cardiac fibrosis, and further decreased transcription and protein expressions of inflammatory factors and fibrosis-related factors. Furthermore, downregulation of cylindromatosis (CYLD) using si-CYLD reversed the results that knockdown of RBP-J inhibited fibrogenesis and the release of inflammatory factors. Altogether, our findings indicated that the blockade of Notch signaling promotes M2 polarization of cardiac macrophages and improves cardiac function by inhibiting the imbalance of fibrotic remodeling after MI.

Indexed as

CYLD expressionfibrotic remodelinginflammationmacrophage polarizationmyocardial infarctionNotch signaling pathway

Identifiers

PMID35111821
PMCPMC8801444
OpenAlexW4206356015

What OpenQuestion holds

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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.