Evidence map›Paper›PMID 25674206›Full record

ArticleInternational journal of clinical and experimental pathology2014

Wnt4/β-catenin signaling pathway modulates balloon-injured carotid artery restenosis via disheveled-1.

Junyi Hua, Yun Xu, Yuzhou He, Xuhong Jiang, Wu Ye, Zhimin Pan

Abstract read
In one paragraph

Article in International journal of clinical and experimental pathology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Article
  2. Article
  3. 4-Molecules (Basel, Switzerland) · 2019
    Article
  4. Article
  5. Review
  6. Article
  7. 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

6 authors.

Junyi HuaDepartment of Cardiology, The First Affiliated Hospital, Zhejiang University of Traditional Chinese Medicine Hangzhou 310006, Zhengjiang, China.
Yun XuDepartment of Cardiology, The First Affiliated Hospital, Zhejiang University of Traditional Chinese Medicine Hangzhou 310006, Zhengjiang, China.
Yuzhou HeDepartment of Cardiology, The First Affiliated Hospital, Zhejiang University of Traditional Chinese Medicine Hangzhou 310006, Zhengjiang, China.
Xuhong JiangDepartment of Cardiology, The First Affiliated Hospital, Zhejiang University of Traditional Chinese Medicine Hangzhou 310006, Zhengjiang, China.
Wu YeDepartment of Cardiology, The First Affiliated Hospital, Zhejiang University of Traditional Chinese Medicine Hangzhou 310006, Zhengjiang, China.
Zhimin PanDepartment of Cardiology, The First Affiliated Hospital, Zhejiang University of Traditional Chinese Medicine Hangzhou 310006, Zhengjiang, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundRestenosis is a common adverse event of endovascular procedures and troubles cardiologists. However, the mechanism underlying restenosis is still not fully understood. To evaluate whether disheveled-1 (Dvl-1) is involved in the Wnt4/β-catenin signaling pathway to participate in the mechanisms of vascular restenosis. METHODOLOGY: Rat model of balloon-injured carotid artery was established and atorvastatin was used to treat artery injury. Vascular smooth muscle cells (VSMC) were isolated from rats and cultured in DMEM exposed to AngII. Down-regulation and overexpression of Dvl-1 were conducted in cells to explore the role underlying its effects on VSMC proliferation and collagen expression. Adenovirus with overexpressing Dvl-1 was injected into rats to evaluate the role of Dvl-1 in artery injury rats.

resultsThe results in vivo found that Wnt4, Dvl-1 and β-catenin expression as well as collagen volume fraction (CVF) in injured artery were significantly increased. The results in vitro showed that Dvl-1 overexpression reversed the treatment effects of atorvastatin on VSMCs proliferation and collagen expression. It was also canceled by overexpressing Dvl-1 that the decrease of β-catenin protein treated with atorvastatin in cells exposed to AngII. In addition, treated artery injury rats with atorvastatin, the group with injection of Ad-Dvl-1 had higher levels of intima thickness, intimal/medial area ratio and CVF.

conclusionDvl-1 was probably a key regulator in the pathway of wnt4/β-catenin to take part in the vascular restenosis partly, and Dvl-1 is a potential gene to anti- restenosis.

Indexed as

Wnt Signaling PathwayAdaptor Proteins, Signal TransducingAngioplasty, BalloonAnimalsbeta CateninBlotting, WesternCarotid Artery InjuriesCells, CulturedDisease Models, AnimalDishevelled ProteinsGraft Occlusion, VascularImmunohistochemistryMuscle, Smooth, VascularMyocytes, Smooth MusclePhosphoproteinsRatsAdaptor Proteins, Signal Transducingbeta CateninCtnnb1 protein, ratDishevelled ProteinsDvl1 protein, ratPhosphoproteinsWnt4 ProteinWnt4 protein, ratdisheveled-1ratRestenosisstatinvascular smooth muscle cellswntβ-catenin

Identifiers

PMID25674206
PMCPMC4314008

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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.