Evidence map›Paper›PMID 23527070›Full record

ArticlePloS one2013

Induction of thoracic aortic remodeling by endothelial-specific deletion of microRNA-21 in mice.

Xing-Yi Zhang, Bao-Rong Shen, Yu-Cheng Zhang, Xue-Jiao Wan, Qing-Ping Yao, Guang-Liang Wu, Ji-Yao Wang, Si-Guo Chen, Zhi-Qiang Yan, Zong-Lai Jiang

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.3field-weighted citation impact, top 21% 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

16 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. microRNA-21 and hypertension.Hypertension research : official journal of the Japanese Society of Hypertension · 2018
    Review
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Review
  14. Article
  15. Endothelial microRNAs and atherosclerosis.Current atherosclerosis reports · 2013
    Review
  16. 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

10 authors at 1 institution in 1 country.

Xing-Yi ZhangInstitute of Mechanobiology & Medical Engineering, School of Life Sciences & Biotechnology, Shanghai Jiao Tong University, Shanghai, China.
Bao-Rong Shen
Yu-Cheng Zhang
Xue-Jiao Wan
Qing-Ping Yao
Guang-Liang Wu
Ji-Yao Wang
Si-Guo Chen
Zhi-Qiang Yan
Zong-Lai Jiang
Shanghai Jiao Tong University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

MicroRNAs (miRs) are known to have an important role in modulating vascular biology. MiR21 was found to be involved in the pathogenesis of proliferative vascular disease. The role of miR21 in endothelial cells (ECs) has well studied in vitro, but the study in vivo remains to be elucidated. In this study, miR21 endothelial-specific knockout mice were generated by Cre/LoxP system. Compared with wild-type mice, the miR21 deletion in ECs resulted in structural and functional remodeling of aorta significantly, such as diastolic pressure dropping, maximal tension depression, endothelium-dependent relaxation impairment, an increase of opening angles and wall-thickness/inner diameter ratio, and compliance decrease, in the miR21 endothelial-specific knockout mice. Furthermore, the miR21 deletion in ECs induced down-regulation of collagen I, collagen III and elastin mRNA and proteins, as well as up-regulation of Smad7 and down-regulation of Smad2/5 in the aorta of miR21 endothelial-specific knockout mice. CTGF and downstream MMP/TIMP changes were also identified to mediate vascular remodeling. The results showed that miR21 is identified as a critical molecule to modulate vascular remodeling, which will help to understand the role of miR21 in vascular biology and the pathogenesis of vascular diseases.

Indexed as

Gene DeletionMicroRNAsAcetylcholineAnimalsAorta, ThoracicBlood PressureCollagenConnective Tissue Growth FactorElastinEndothelium, VascularExtracellular MatrixFemaleGene OrderGene TargetingMaleMatrix MetalloproteinasesAcetylcholineCollagenConnective Tissue Growth FactorElastinMatrix MetalloproteinasesMicroRNAsMIRN21 microRNA, mouseSmad2 ProteinSmad5 ProteinTransforming Growth Factor beta1

Identifiers

PMID23527070
PMCPMC3601125
OpenAlexW1963508845

What OpenQuestion holds

Textmetadata
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.