Evidence map›Paper›PMID 31064890›Full record

ArticleAging2019

MiR-191 inhibit angiogenesis after acute ischemic stroke targeting VEZF1.

Kang Du, Can Zhao, Li Wang, Yue Wang, Kang-Zhen Zhang, Xi-Yu Shen, Hui-Xian Sun, Wei Gao, Xiang Lu

Open access · greenAbstract read
In one paragraph

Article in Aging, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
6.9field-weighted citation impact, top 3% 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

44 citing papers in PubMed, 67 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. Role of miRNAs in neurovascular injury and repair.Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism · 2024
    Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Review
  13. Article
  14. Angiogenesis after ischemic stroke.Acta pharmacologica Sinica · 2023
    Review
  15. Article
  16. Specific microRNA Signature Kinetics inInternational journal of molecular sciences · 2023
    Article
  17. Article
  18. Article
  19. Review
  20. 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

9 authors at 1 institution in 1 country.

Kang Du *Department of Geriatrics, Sir Run Run Hospital, Nanjing Medical University, Nanjing, Jiangsu Province 211166, China.
Can Zhao *Department of Geriatrics, Sir Run Run Hospital, Nanjing Medical University, Nanjing, Jiangsu Province 211166, China.
Li WangDepartment of Geriatrics, Sir Run Run Hospital, Nanjing Medical University, Nanjing, Jiangsu Province 211166, China.
Yue WangDepartment of Geriatrics, Sir Run Run Hospital, Nanjing Medical University, Nanjing, Jiangsu Province 211166, China.
Kang-Zhen ZhangDepartment of Geriatrics, Sir Run Run Hospital, Nanjing Medical University, Nanjing, Jiangsu Province 211166, China.
Xi-Yu ShenDepartment of Geriatrics, Sir Run Run Hospital, Nanjing Medical University, Nanjing, Jiangsu Province 211166, China.
Hui-Xian SunDepartment of Geriatrics, Sir Run Run Hospital, Nanjing Medical University, Nanjing, Jiangsu Province 211166, China.
Wei GaoDepartment of Geriatrics, Sir Run Run Hospital, Nanjing Medical University, Nanjing, Jiangsu Province 211166, China.
Xiang LuDepartment of Geriatrics, Sir Run Run Hospital, Nanjing Medical University, Nanjing, Jiangsu Province 211166, China.
Nanjing Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Acute ischemic stroke (AIS) is a major public health problem in China. Impaired angiogenesis plays crucial roles in the development of ischemic cerebral injury. Recent studies have identified that microRNAs (miRNAs) are important regulators of angiogenesis, but little is known the exact effects of angiogenesis-associated miRNAs in AIS. In the present study, we detected the expression levels of angiogenesis-associated miRNAs in AIS patients, middle cerebral artery occlusion (MCAO) rats, and oxygen-glucose deprivation/reoxygenation (OGD/R) human umbilical vein endothelial cells (HUVECs). MiR-191 was increased in the plasma of AIS patients, OGD/R HUVECs, and the plasma and brain of MCAO rats. Over-expression of miR-191 promoted apoptosis, but reduced the proliferation, migration, tube-forming and spheroid sprouting activity in HUVECs OGD/R model. Mechanically, vascular endothelial zinc finger 1 (VEZF1) was identified as the direct target of miR-191, and could be regulated by miR-191 at post-translational level. In vivo studies applying miR-191 antagomir demonstrated that inhibition of miR-191 reduced infarction volume in MCAO rats. In conclusion, our data reveal a novel role of miR-191 in promoting ischemic brain injury through inhibiting angiogenesis via targeting VEZF1. Therefore, miR-191 may serve as a biomarker or a therapeutic target for AIS.

Indexed as

AgedAnimalsBiomarkersBrain IschemiaDNA-Binding ProteinsFemaleGene Expression RegulationHumansHuman Umbilical Vein Endothelial CellsInfarction, Middle Cerebral ArteryMaleMicroRNAsNeovascularization, PhysiologicRatsRats, Sprague-DawleySignal TransductionBiomarkersDNA-Binding ProteinsMicroRNAsMIRN191 microRNA, humanTranscription FactorsVEZF1 protein, humanacute strokeangiogenesis factormiR-191VEZF1

Identifiers

PMID31064890
PMCPMC6535071
OpenAlexW2944394135

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.