Evidence map›Paper›PMID 33860034›Full record

ArticleBioMed research international2021

miR-543 Inhibits the Occurrence and Development of Intrauterine Adhesion by Inhibiting the Proliferation, Migration, and Invasion of Endometrial Cells.

Xin Liu, Qian Xu, Chao Chen, Hua Duan

Open access · hybridAbstract read
In one paragraph

Article in BioMed research international, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

6 citing papers in PubMed, 13 citations in OpenAlex.

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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

4 authors at 1 institution in 1 country.

Xin LiuBeijing Obstetrics and Gynecology Hospital, Capital Medical University, Gynecological Mini-Invasive Center, 17 qihelou st, Dongcheng District, Beijing 100006, China.
Qian XuBeijing Obstetrics and Gynecology Hospital, Capital Medical University, Gynecological Mini-Invasive Center, 17 qihelou st, Dongcheng District, Beijing 100006, China.
Chao ChenBeijing Obstetrics and Gynecology Hospital, Capital Medical University, Gynecological Mini-Invasive Center, 17 qihelou st, Dongcheng District, Beijing 100006, China.
Hua DuanBeijing Obstetrics and Gynecology Hospital, Capital Medical University, Gynecological Mini-Invasive Center, 17 qihelou st, Dongcheng District, Beijing 100006, China.ORCID https://orcid.org/0000-0002-9428-7561
Capital Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo explore the function of miR-543 in endometrial cells and the possible mechanism of regulating the occurrence and development of intrauterine adhesion.

methodEndometrial epithelial cells and endometrial adenocarcinoma cells were transfected with miR-543 mimics and miR-543 inhibitor as the experimental group and were tested with the control group, using the CCK-8 method, scratch test, and Transwell assay, and flow cytometry was used to detect the proliferation, migration, invasion, and apoptosis of cells. RT-qPCR and Western blot were used to detect the expression of corresponding mRNA and protein.

resultsAfter the overexpression of miR-543, endometrial epithelial cells and endometrial adenocarcinoma cells have reduced migratory, proliferative, and invasive capabilities, while the apoptosis rate has increased significantly. The mRNA expression of

conclusionDuring the formation of intrauterine adhesions, the expression of

Indexed as

Antigens, CDApoptosisBase SequenceCadherinsCell Line, TumorCell MovementCell ProliferationEndometriumEpithelial CellsFemaleFibrosisGene Expression Regulation, NeoplasticHumansMicroRNAsNeoplasm InvasivenessTissue AdhesionsAntigens, CDCadherinsCDH2 protein, humanMicroRNAsMIRN543 microRNA, human

Identifiers

PMID33860034
PMCPMC8024079
OpenAlexW3149635204

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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.