Evidence map›Paper›PMID 32867783›Full record

ArticleJournal of translational medicine2020

MiR-199a-3p/5p participated in TGF-β and EGF induced EMT by targeting DUSP5/MAP3K11 in pterygium.

Siying He, Yifang Huang, Shiqi Dong, Chen Qiao, Guohua Yang, Shuai Zhang, Chen Wang, Yuting Xu, Fang Zheng, Ming Yan

Open access · goldAbstract read
In one paragraph

Article in Journal of translational medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.0field-weighted citation impact, top 11% 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

22 citing papers in PubMed, 30 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

10 authors at 3 institutions in 1 country.

Siying HeCenter for Gene Diagnosis, and Clinical Laboratory, Zhongnan Hospital of Wuhan University, Donghu Rd 169#, Wuhan, 430071, China.
Yifang HuangDepartment of Clinical Laboratory, the First Affiliated Hospital of Guangxi Medical University, Nanning, 530021, Guangxi, China.
Shiqi DongDepartment of Ophthalmology, Zhongnan Hospital of Wuhan University, Wuhan, 430071, Hubei, China.
Chen QiaoDepartment of Corneal, Hankou Aier Eye Hospital, Wuhan, 430024, Hubei, China.
Guohua YangDemonstration Center for Experimental Basic Medicine Education, Wuhan University, Wuhan, 430071, Hubei, China.
Shuai ZhangCenter for Gene Diagnosis, and Clinical Laboratory, Zhongnan Hospital of Wuhan University, Donghu Rd 169#, Wuhan, 430071, China.
Chen WangCenter for Gene Diagnosis, and Clinical Laboratory, Zhongnan Hospital of Wuhan University, Donghu Rd 169#, Wuhan, 430071, China.
Yuting XuDepartment of Ophthalmology, Zhongnan Hospital of Wuhan University, Wuhan, 430071, Hubei, China.
Fang ZhengCenter for Gene Diagnosis, and Clinical Laboratory, Zhongnan Hospital of Wuhan University, Donghu Rd 169#, Wuhan, 430071, China. zhengfang@whu.edu.cn.
Ming YanDepartment of Ophthalmology, Zhongnan Hospital of Wuhan University, Wuhan, 430071, Hubei, China. yanming72@whu.edu.cn.ORCID 0000-0001-9150-0614
Wuhan University · CNGuangxi Medical University · CNWuhan Hankou Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundRecently, it has been reported that miRNA is involved in pterygium, however the exact underlying mechanism in pterygium is unrevealed and require further investigation.

methodsThe differential expression of miRNA in pterygium was profiled using microarray and validated with quantitative real-time polymerase chain reaction (qRT-PCR). Human conjunctival epithelial cells (HCEs) were cultured and treated with transforming growth factor β (TGF-β) and epidermal growth factor (EGF) and transfected with miR-199a-3p/5p mimic and inhibitor. Markers of epithelial-mesenchymal transition (EMT) in HCEs were detected using western blot and immunohistochemistry. Cell migration ability was determined using wound healing and transwell assay, while apoptosis was determined by flow cytometry. The target genes of miR-199a were confirmed by the dual-luciferase reporter assay.

resultsTGF-β and EGF could induced EMT in HCEs and increase miR-199a-3p/5p but suppress target genes, DUSP5 and MAP3K11. With the occurrence of EMT, cell migration ability was enhanced, and apoptosis was impeded. Promoting miR-199a-3p/5p expression could induce EMT in HCEs without TGF-β and EGF, while suppressing miR-199a-3p/5p could inhibit EMT in TGF-β and EGF induced HCEs. In a word, TGF-β and EGF induced EMT could be regulated with miR-199a-3p/5p-DUSP5/MAP3K11 axes. The validated results in tissues showed that, compared with control conjunctival tissues, miR-199a-3p/5p were more overexpressed in pterygium, while DUSP5/MAP3K11 were lower expressed. In addition, bioinformatics analysis indicated the miR-199a-3p/5p-DUSP5/MAP3K11 was belong to MAPK signalling pathway.

conclusionsTGF-β and EGF induce EMT of HCEs through miR-199a-3p/5p-DUSP5/MAP3K11 axes, which explains the pathogenesis of EMT in pterygium and may provide new targets for pterygium prevention and therapy.

Indexed as

MicroRNAsPterygiumDual-Specificity PhosphatasesEpidermal Growth FactorEpithelial-Mesenchymal TransitionHumansTransforming Growth Factor betaDual-Specificity PhosphatasesDUSP5 protein, humanEpidermal Growth FactorMicroRNAsTransforming Growth Factor betaDUSP5EMTMAP3K11miR-199aPterygium

Identifiers

PMID32867783
PMCPMC7461358
OpenAlexW3081572383

What OpenQuestion holds

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LicenceCC BY
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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.