Evidence map›Paper›PMID 31814903›Full record

ArticleAmerican journal of translational research2019

miR-1 and miR-802 regulate mesenchymal-epithelial transition during kidney development by regulating Wnt-4/β-catenin signaling.

Lili Zhang, Tao Wu, Sen Qiao

Abstract read
In one paragraph

Article in American journal of translational research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. miR-802-5p is a key regulator in diabetic kidney disease.Journal of research in medical sciences : the official journal of Isfahan University of Medical Sciences · 2023
    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

3 authors.

Lili ZhangDepartment of Laboratory Medicine, The Affiliated Hospital of Zunyi Medical University Zunyi 563003, P. R. China.
Tao WuDepartment of Urology, The Affiliated Hospital of Zunyi Medical University Zunyi 563003, P. R. China.
Sen QiaoDepartment of Laboratory Medicine, The Affiliated Hospital of Zunyi Medical University Zunyi 563003, P. R. China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveMesenchymal-epithelial transition (MET) is an important part of kidney development. However, the role of microRNA (miRNA) in MET and the regulating mechanism is still not well known. MATERIALS AND

methodsqRT-PCR and western blot were performed to detect the expression of miR-1 and miR-802 and related protein expression. Luciferase reporter assay and western blot were used to identify the target of miR-1 and miR-802. Confocal microscopy was used to analyze the MET process.

resultsWe demonstrated that miR-1 expression was downregulated and miR-802 expression was upregulated during kidney development. And during the process, proteins levels of Wnt-4 and β-catenin changed significantly. In MDCK cells, overexpression of Wnt-4 inhibited the expression of β-catenin, and promote the MET, and overexpression of β-catenin inhibited MET. Further studies suggested that miR-1 and miR-802 regulated MET by binding to Wnt-4 and β-catenin mRNA, regulated the expression of Wnt-4 and β-catenin. In conclusion, miR-1 and miR-802 regulate MET during kidney development by regulating Wnt-4/β-catenin signaling.

Indexed as

Mesenchymal-epithelial transitionmicroRNAsmiR-1miR-802Wnt-4/β-catenin signaling

Identifiers

PMID31814903
PMCPMC6895509

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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.