Evidence map›Paper›PMID 33150936›Full record

ArticleBioscience reports2020

miR-200-3p suppresses cell proliferation and reduces apoptosis in diabetic retinopathy via blocking the TGF-β2/Smad pathway.

Liping Xue, Cheng Xiong, Juanjuan Li, Yuling Ren, Liwei Zhang, Kangwei Jiao, Chen Chen, Peng Ding

Open access · goldAbstract read
In one paragraph

Article in Bioscience reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.2field-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

25 citing papers in PubMed, 35 citations in OpenAlex.

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  9. Muscle-Derived miR-200a-3p Through Light-Intensity Exercise May Contribute to Improve Memory Dysfunction in Type 2 Diabetic Mice.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2025
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  16. TGF-β Signaling Pathways in the Development of Diabetic Retinopathy.International journal of molecular sciences · 2024
    Review
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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

8 authors at 2 institutions in 1 country.

Liping Xue *Department of Ophthalmology, Yunnan Eye Institute, Yunnan No.2 Provincial People's Hospital, Kunming 650021, Yunnan, China.
Cheng Xiong *Department of Ophthalmology, Yunnan Eye Institute, Yunnan No.2 Provincial People's Hospital, Kunming 650021, Yunnan, China.
Juanjuan LiDepartment of Ophthalmology, Yunnan Eye Institute, Yunnan No.2 Provincial People's Hospital, Kunming 650021, Yunnan, China.
Yuling RenDepartment of Ophthalmology, Yunnan Eye Institute, Yunnan No.2 Provincial People's Hospital, Kunming 650021, Yunnan, China.
Liwei ZhangDepartment of Ophthalmology, Yunnan Eye Institute, Yunnan No.2 Provincial People's Hospital, Kunming 650021, Yunnan, China.
Kangwei JiaoDepartment of Ophthalmology, Yunnan Eye Institute, Yunnan No.2 Provincial People's Hospital, Kunming 650021, Yunnan, China.
Chen ChenDepartment of Ophthalmology, Yunnan Eye Institute, Yunnan No.2 Provincial People's Hospital, Kunming 650021, Yunnan, China.
Peng DingDepartment of Neurosurgery, The First Affiliated Hospital of Kunming Medical University, Kunming 650032, Yunnan, China.
Second People's Hospital of Yunnan Province · CNKunming Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Increasing evidence has shown that microRNAs (miRNAs) play an important role in the pathogenesis of diabetic retinopathy (DR). However, the role and mechanism of miRNA in regulating high glucose (HG)-induced ARPE-19 cell injury are still not well understood. The present study aimed to investigate the effects of miR-200a-3p on DR progression and reveal the underlying mechanisms of their effects. In the present study, we observed that miR-200a-3p was significantly decreased, while transforming growth factor-β2 (TGF-β2) expression was up-regulated in ARPE-19 cells treated with HG and retina tissues of DR rats. Subsequently, overexpression of miR-200a-3p significantly promoted cell proliferation, reduced apoptosis, as well as inhibited the levels of inflammatory cytokines secreted, matrix metalloprotease 2/9 (MMP2/9), and vascular endothelial growth factor (VEGF) in HG-injured ARPE-19 cells. Moreover, miR-200a-3p was proved to target TGF-β2 mRNA by binding to its 3' untranslated region (3'UTR) using a luciferase reporter assay. Mechanistically, overexpression of miR-200a-3p reduced HG-induced ARPE-19 cell injury and reduced inflammatory cytokines secreted, as well as down-regulated the expression of VEGF via inactivation of the TGF-β2/Smad pathway in vitro. In vivo experiments, up-regulation of miR-200a-3p ameliorated retinal neovascularization and inflammation of DR rats. In conclusion, our findings demonstrated that miR-200a-3p-elevated prevented DR progression by blocking the TGF-β2/Smad pathway, providing a new therapeutic biomarker for DR treatment in the clinic.

Indexed as

ApoptosisCell Proliferation3' Untranslated RegionsAnimalsBinding SitesCell LineDiabetes Mellitus, ExperimentalDiabetic RetinopathyGene Expression RegulationGlucoseHumansMaleMicroRNAsRats, WistarRetinal Pigment EpitheliumSignal Transduction3' Untranslated RegionsGlucoseMicroRNAsMIRN200 microRNA, humanMIRN200 microRNA, ratSmad ProteinsTGFB2 protein, humanTgfb2 protein, ratTransforming Growth Factor beta2diabetic retinopathyhigh glucosemiR-200a-3pTGF-β2/Smad pathway

Identifiers

PMID33150936
PMCPMC7689656
OpenAlexW3097666122

What OpenQuestion holds

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LicenceCC BY
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.