Evidence mapPaperPMID 40580205Full record

ArticleAngiogenesis2025

Semaphorin 3A protects against thoracic aortic aneurysm dissection by suppressing aortic angiogenesis.

Li-Fei Wu, Jiao-Jiao Zhang, Xing Zhang, De-Ping Wang, Zhi-Fa Zheng, Jing Shen, Ying Zhou, Li-Juan Gao, Xuan Shang, Jun-Ya Ning and 12 more

Abstract read
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In one paragraph

Article in Angiogenesis, 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. Article
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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

22 authors.

Li-Fei WuKey Laboratory of Cellular Physiology, Shanxi Medical University, Ministry of Education, Taiyuan, China.
Jiao-Jiao ZhangKey Laboratory of Cellular Physiology, Shanxi Medical University, Ministry of Education, Taiyuan, China.
Xing ZhangKey Laboratory of Cellular Physiology, Shanxi Medical University, Ministry of Education, Taiyuan, China.
De-Ping WangKey Laboratory of Cellular Physiology, Shanxi Medical University, Ministry of Education, Taiyuan, China.
Zhi-Fa ZhengDepartment of Cardiovascular Surgery, Shanxi Bethune Hospital, Taiyuan, China.
Jing ShenKey Laboratory of Cellular Physiology, Shanxi Medical University, Ministry of Education, Taiyuan, China.
Ying ZhouKey Laboratory of Cellular Physiology, Shanxi Medical University, Ministry of Education, Taiyuan, China.
Li-Juan GaoKey Laboratory of Cellular Physiology, Shanxi Medical University, Ministry of Education, Taiyuan, China.
Xuan ShangKey Laboratory of Cellular Physiology, Shanxi Medical University, Ministry of Education, Taiyuan, China.
Jun-Ya NingKey Laboratory of Cellular Physiology, Shanxi Medical University, Ministry of Education, Taiyuan, China.
Qing-Hua LiuKey Laboratory of Cellular Physiology, Shanxi Medical University, Ministry of Education, Taiyuan, China.
Lan ZhouKey Laboratory of Cellular Physiology, Shanxi Medical University, Ministry of Education, Taiyuan, China.
Zhang-Rong JiaKey Laboratory of Cellular Physiology, Shanxi Medical University, Ministry of Education, Taiyuan, China.
Jia-Song ChangKey Laboratory of Cellular Physiology, Shanxi Medical University, Ministry of Education, Taiyuan, China.
Jian-Yun ShiKey Laboratory of Cellular Physiology, Shanxi Medical University, Ministry of Education, Taiyuan, China.
Shuang WangKey Laboratory of Cellular Physiology, Shanxi Medical University, Ministry of Education, Taiyuan, China.
Teng SunKey Laboratory of Cellular Physiology, Shanxi Medical University, Ministry of Education, Taiyuan, China.
Xue-Ning WangDepartment of Cardiovascular Surgery, Shanxi Bethune Hospital, Taiyuan, China.
Zhi-Fang WuDepartment of Nuclear Medicine, The First Hospital of Shanxi Medical University, Molecular Imaging Precision Medical Collaborative Innovation Center, Shanxi Medical University, Taiyuan, China.
Si-Jin LiDepartment of Nuclear Medicine, The First Hospital of Shanxi Medical University, Molecular Imaging Precision Medical Collaborative Innovation Center, Shanxi Medical University, Taiyuan, China. lisjnm123@163.com.
Xin ZhouKey Laboratory of Cellular Physiology, Shanxi Medical University, Ministry of Education, Taiyuan, China. xzhou@sxmu.edu.cn.
Ji-Min CaoKey Laboratory of Cellular Physiology, Shanxi Medical University, Ministry of Education, Taiyuan, China. caojimin@sxmu.edu.cn.

Funding

National Natural Science Foundation of China 81670313National Natural Science Foundation of China 82170523, 81670313, U22A6008National Natural Science Foundation of China U22A6008
6 · The paper itself

Abstract

Thoracic aortic aneurysm (TAA) is life-threatening once developing to sudden dissection (TAAD) or rupture. The pathogenesis of TAA remains poorly understood and there is no effective pharmacologic therapy. Increased aortic angiogenesis has been recognized as a key factor contributing to TAA formation, yet the regulatory mechanisms governing this process remain unclear. Here we found that the mRNA and protein levels of Sema3A were significantly decreased in human TAA/TAAD tissues compared to non-TAA aortic tissues. Global or vascular smooth muscle cells (VSMCs)-specific overexpression of Sema3A significantly alleviated the progression of β-aminopropionitrile fumarate (BAPN)-induced TAA and reduced TAAD incidence, whereas VSMCs-specific knockout of Sema3A aggravated TAA and increased TAAD incidence, in mice. Sema3A was leadingly expressed in the VSMCs, and the VSMCs-derived Sema3A protected TAA mainly via binding to NRP1 on the endothelial cells (ECs) and inhibiting the downstream ERK signaling, and thereby suppressing aortic neovascularization, inflammation and extracellular matrix (ECM) degradation. Administration of recombinant Sema3A protein hindered TAA progression and reduced TAAD incidence in mice. In summary, we demonstrated that Sema3A is a potential endogenous protective factor for TAA. Downregulation of Sema3A promotes TAA progression and TAAD attack, whereas upregulation of Sema3A or administration of recombinant Sema3A protein alleviates TAA and reduces TAAD incidence. The protection of Sema3A on TAA depends on the VSMC-EC crosstalk and activation of endothelial NRP1-ERK signaling, and thereby the suppression of angiogenesis and angiogenesis-associated inflammation and ECM degradation.

Indexed as

Aortic Aneurysm, ThoracicAortic DissectionNeovascularization, PathologicSemaphorin-3AAngiogenesisAnimalsHumansMaleMiceMice, Inbred C57BLMice, KnockoutMuscle, Smooth, VascularMyocytes, Smooth MuscleNeuropilin-1Neuropilin-1SEMA3A protein, humanSemaphorin-3AAngiogenesisEndothelial cellNRP1Semaphorin 3AThoracic aortic aneurysmVascular smooth muscle cell

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What Socratic holds

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Registered trials

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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 Socratic graph.