Evidence map›Paper›PMID 29948755›Full record

ArticleJournal of thrombosis and thrombolysis2018

microRNAs regulate nitric oxide release from endothelial cells by targeting NOS3.

Ji-Zheng Qin, Shao-Jie Wang, Chun Xia

Abstract read
PubMed Publisher
In one paragraph

Article in Journal of thrombosis and thrombolysis, 2018. 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
0.6field-weighted citation impact, top 37% 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, 29 citations in OpenAlex.

  1. Review
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  10. Article
  11. Review
  12. Micro RNAs in Regulation of Cellular Redox Homeostasis.International journal of molecular sciences · 2021
    Review
  13. Article
  14. Article
  15. MicroRNA and their target mRNAs change expression in whole blood of patients after intracerebral hemorrhage.Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism · 2020
    Article
  16. SOD1ASN neuro
    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

3 authors at 1 institution in 1 country.

Ji-Zheng QinZhongshan Hospital, Xiamen University, Hubin South Road 201, Xiamen, 361004, Fujian, China.ORCID http://orcid.org/0000-0001-7888-4625
Shao-Jie WangZhongshan Hospital, Xiamen University, Hubin South Road 201, Xiamen, 361004, Fujian, China.
Chun XiaZhongshan Hospital, Xiamen University, Hubin South Road 201, Xiamen, 361004, Fujian, China. chunxia99@aliyun.com.
Zhongshan Hospital of Xiamen University · CN

Funding

The National Science Foundation of Fujian, China 2016J01622The National Science Foundation of Fujian, China 2016-ZQN-86
6 · The paper itself

Abstract

Endothelial nitric oxide synthase (eNOS) encoded by nitric oxide synthase 3 (NOS3), can generate nitric oxide (NO) which serves as an important deterrent to the pathogenesis of thrombosis by modulating the activation, adhesion and aggregate formation of platelets. Three serum miRNAs (miR-195, miR-532 and miR-582) have been suggested as biomarkers for the diagnosis of deep vein thrombosis (DVT), however their potential roles in DVT is not clear. The effect of miRNAs inhibiting the expression of NOS3 was evaluated in vitro. miR-195, miR-532 and miR-582 mimic, inhibitor, and control miRNAs were transfected into endothelial cells. The roles of miR-195, miR-532 and miR-582 regulating the expression of eNOS were evaluated by real-time quantitative PCR, Western Blotting and luciferase reporter assays. NO release was measured by Griess method. We confirmed NOS3 as a direct target of miR-195 and miR-582, which binds to the 3'-UTR of NOS3 mRNA in endothelial cells. A significantly inverse correlation between these two miRNAs and eNOS expression was detected. NO release from endothelial cells was decreased when the expression level of miR-195 and miR-582 was up-regulated. These findings indicated that miR-195 and miR-582 regulated NO release by targeting 3'-UTR of NOS3 post-transcriptionally in endothelial cells. Therefore, miR-195 and miR-582 might play an important role in maintaining endothelial NO bioavailability and could be a novel target for treatment of thrombotic diseases.

Indexed as

3' Untranslated RegionsBinding SitesCells, CulturedEndothelial CellsHumansMicroRNAsNitric OxideNitric Oxide Synthase Type IIITransfection3' Untranslated RegionsMicroRNAsMIRN195 microRNA, humanMIRN532 microRNA, humanMIRN582 microRNA, humanNitric OxideNitric Oxide Synthase Type IIINOS3 protein, humanMicroRNANitric oxideNitric oxide synthase 3PathogenesisThrombosis

Identifiers

PMID29948755
OpenAlexW2807891368

What OpenQuestion holds

Textmetadata
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.