Evidence map›Paper›PMID 26722433›Full record

ArticleInternational journal of clinical and experimental pathology2015

Activation of SHH signaling pathway promotes vasculogenesis in post-myocardial ischemic-reperfusion injury.

Wei Guo, Xin Yi, Faxin Ren, Liwen Liu, Suning Wu, Jun Yang

Abstract read
In one paragraph

Article in International journal of clinical and experimental pathology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

  1. Review
  2. Article
  3. Sonic hedgehog is expressed in human brain arteriovenous malformations and induces arteriovenous malformations in vivo.Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism · 2021
    Article
  4. Article
  5. The Hedgehog Signaling Pathway in Ischemic Tissues.International journal of molecular sciences · 2019
    Review
  6. Review
  7. Article
  8. Crosstalk between Stem and Progenitor Cellular Mediators with Special Emphasis on Vasculogenesis.Transfusion medicine and hemotherapy : offizielles Organ der Deutschen Gesellschaft fur Transfusionsmedizin und Immunhamatologie · 2017
    Review
  9. 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

6 authors.

Wei GuoQingdao University Qingdao 266000, Shandong Province, China ; Department of Geratology, Jining NO. 1 People's Hospital Jining 272011, Shandong Province, China.
Xin YiDepartment of Laboratory, Jining NO. 1 People's Hospital Jining 272011, Shandong Province, China.
Faxin RenDepartment of Cardiology, Affiliated Yantai Yuhuangding Hospital, Medical College of Qingdao University Yantai 264000, Shandong Province, China.
Liwen LiuDepartment of Geratology, Jining NO. 1 People's Hospital Jining 272011, Shandong Province, China.
Suning WuDepartment of Geratology, Jining NO. 1 People's Hospital Jining 272011, Shandong Province, China.
Jun YangDepartment of Cardiology, Affiliated Yantai Yuhuangding Hospital, Medical College of Qingdao University Yantai 264000, Shandong Province, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study aimed to investigate the potential roles of sonic Hedgehog (SHH) expression in vasculogenesis in post-myocardial ischemic-reperfusion injury (MIRI) and its underlying mechanism. Cardiac microvascular endothelial cells (CMECs) isolated from the SD rat hearts tissues were used to construct the MIRI model. mRNA level of SHH in control cells and MIRI cells was detected using RT-PCR analysis. Furthermore, effects of SHH expression on CMECs viability and apoptosis were analyzed using MTT assay and Annexin-V-FITC kit respectively. Moreover, effects of SHH expression on the pathway signal proteins expression was analyzed using ELISA and western blotting. mRNA level of SHH was significantly decreased compared to the controls (P<0.05). Besides, CMECs viability was significantly increased while cell apoptosis was decreased by SHH application compared with the controls (P<0.05). Vasculogenesis-related factors including VEGF, FGF and Ang were significantly increased by SHH application, as well as the SHH signal proteins including Patch-1, Gli1, Gli2 and SMO (P<0.05). However, these effects of SHH application on biological factors levels were reversed by the SHH inhibitor application. This study suggested that SHH over expression may play a pivotal contribute role in vasculogenesis through activating the SHH signals in post-MIRI.

Indexed as

AnimalsApoptosisBlotting, WesternCells, CulturedEnzyme-Linked Immunosorbent AssayHedgehog ProteinsMyocardial IschemiaMyocardial Reperfusion InjuryNeovascularization, PhysiologicRatsRats, Sprague-DawleyReal-Time Polymerase Chain ReactionSignal TransductionHedgehog ProteinsShh protein, ratcell apoptosiscell viabilityMyocardial ischemic-reperfusion injurySHHvasculogenesis

Identifiers

PMID26722433
PMCPMC4680378

What OpenQuestion 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 OpenQuestion graph.