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心血管疾病中EGR1的综合文献计量学与可视化分析

A Comprehensive Bibliometric and Visual Analysis of EGR1 in Cardiovascular Disease.

作者信息

Dong Na, Yue Hongmei

机构信息

The First School of Clinical Medicine, Lanzhou University, Lanzhou, 730000, China.

Department of Respiratory and Critical Care Medicine, The First Hospital of Lanzhou University, Lanzhou, 730000, China.

出版信息

Mol Biotechnol. 2025 Aug 29. doi: 10.1007/s12033-025-01493-7.


DOI:10.1007/s12033-025-01493-7
PMID:40880050
Abstract

Early Growth Response 1 (EGR1) is a crucial transcription factor that regulates diverse cellular processes, including growth, differentiation, proliferation, inflammation, apoptosis, and autophagy. It plays a vital role in maintaining cardiac homeostasis and is deeply implicated in the pathological mechanisms leading to cardiomyocyte death, making it a promising therapeutic target for cardiovascular diseases. To better understand the research landscape of EGR1 in this context, we conducted a bibliometric analysis using data from the Web of Science Core Collection (WoSCC) covering the period from 2014 to 2024, retrieved on 31 December 2024. A total of 2,112 publications related to EGR1 were identified, of which 173 specifically addressed cardiovascular disease and were published across 126 journals. Global research output on this topic has shown fluctuating growth over the past decade, with China contributing the most publications and citations. The Institut national de la santé et de la recherche médicale (Inserm) emerged as the most productive institution. Zhang Y authored the highest number of papers, while Wang J received the most citations. Scientific Reports was the most prolific journal, whereas the Journal of Biological Chemistry was the most influential in terms of citation metrics. Keyword co-occurrence and cluster analysis revealed major research themes such as apoptosis, inflammation, oxidative stress, angiogenesis, and autophagy. These findings provide a comprehensive overview of EGR1-related cardiovascular research and offer a valuable reference for future investigations into its mechanisms and therapeutic potential.

摘要

早期生长反应因子1(EGR1)是一种关键的转录因子,可调节多种细胞过程,包括生长、分化、增殖、炎症、凋亡和自噬。它在维持心脏稳态中起着至关重要的作用,并与导致心肌细胞死亡的病理机制密切相关,使其成为心血管疾病有前景的治疗靶点。为了更好地了解EGR1在这方面的研究概况,我们使用来自科学引文索引核心合集(WoSCC)的数据进行了文献计量分析,数据涵盖2014年至2024年期间,并于2024年12月31日检索。共识别出2112篇与EGR1相关的出版物,其中173篇专门涉及心血管疾病,发表在126种期刊上。过去十年全球关于该主题的研究产出呈现波动增长,中国的出版物和被引次数最多。法国国家健康与医学研究院(Inserm)是产出最多的机构。张Y发表的论文数量最多,而王J获得的被引次数最多。《科学报告》是发文量最多的期刊,而《生物化学杂志》在引文指标方面最具影响力。关键词共现和聚类分析揭示了凋亡、炎症、氧化应激、血管生成和自噬等主要研究主题。这些发现全面概述了与EGR1相关的心血管研究,并为未来对其机制和治疗潜力的研究提供了有价值的参考。

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A Comprehensive Bibliometric and Visual Analysis of EGR1 in Cardiovascular Disease.

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本文引用的文献

[1]
Current perspectives and trends of CD39-CD73-eAdo/A2aR research in tumor microenvironment: a bibliometric analysis.

Front Immunol. 2024

[2]
Role of early growth response 1 in inflammation-associated lung diseases.

Am J Physiol Lung Cell Mol Physiol. 2023-8-1

[3]
Early growth response-1: Key mediators of cell death and novel targets for cardiovascular disease therapy.

Front Cardiovasc Med. 2023-3-28

[4]
Interdependent Nuclear Co-Trafficking of ASPP1 and p53 Aggravates Cardiac Ischemia/Reperfusion Injury.

Circ Res. 2023-1-20

[5]
The Epigenetic Role of MiRNAs in Endocrine Crosstalk Between the Cardiovascular System and Adipose Tissue: A Bidirectional View.

Front Cell Dev Biol. 2022-7-4

[6]
EGR1 Upregulation during Encephalitic Viral Infections Contributes to Inflammation and Cell Death.

Viruses. 2022-6-2

[7]
Cardioprotective Effect of circ_SMG6 Knockdown against Myocardial Ischemia/Reperfusion Injury Correlates with miR-138-5p-Mediated EGR1/TLR4/TRIF Inactivation.

Oxid Med Cell Longev. 2022

[8]
Circ_ZNF512-Mediated miR-181d-5p Inhibition Limits Cardiomyocyte Autophagy and Promotes Myocardial Ischemia/Reperfusion Injury through an EGR1/mTORC1/TFEB-Based Mechanism.

J Med Chem. 2022-2-10

[9]
Early Growth Response-1, an Integrative Sensor in Cardiovascular and Inflammatory Disease.

J Am Heart Assoc. 2021-11-16

[10]
Serine 26 in Early Growth Response-1 Is Critical for Endothelial Proliferation, Migration, and Network Formation.

J Am Heart Assoc. 2021-9-21

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