Evidence map›Paper›PMID 35441575›Full record

ArticleBioengineered2022

MiR-192 attenuates high glucose-induced pyroptosis in retinal pigment epithelial cells via inflammasome modulation.

Cao Gu, Hongjun Zhang, Qing Li, Shaofei Zhao, Yu Gao

Open access · goldAbstract read
In one paragraph

Article in Bioengineered, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
3.1field-weighted citation impact, top 7% 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

14 citing papers in PubMed, 36 citations in OpenAlex.

  1. Review
  2. Review
  3. [Mechanisms of pyroptosis in metabolic diseases].Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences · 2025
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  7. Article
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  9. Article
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  12. Diabetic Neuropathy of the Retina and Inflammation: Perspectives.International journal of molecular sciences · 2023
    Review
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  14. Review
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

5 authors at 2 institutions in 1 country.

Cao GuDepartment of Ophthalmology, Changhai Hospital, First Affiliated Hospital of Naval Medical University (Second Military Medical University), Shanghai, China.
Hongjun ZhangDepartment of Ophthalmology, Minhang Branch of Zhongshan Hospital Affiliated to Fudan University, Shanghai, China.
Qing LiDepartment of Ophthalmology, Changhai Hospital, First Affiliated Hospital of Naval Medical University (Second Military Medical University), Shanghai, China.
Shaofei ZhaoDepartment of Ophthalmology, Changhai Hospital, First Affiliated Hospital of Naval Medical University (Second Military Medical University), Shanghai, China.
Yu GaoDepartment of Ophthalmology, Changhai Hospital, First Affiliated Hospital of Naval Medical University (Second Military Medical University), Shanghai, China.ORCID 0000-0002-2366-3187
Second Military Medical University · CNFudan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Diabetic retinopathy is one of the most characteristic complications of diabetes mellitus, and pyroptosis plays acrucial role in the onset and development of diabetic retinopathy. Although microRNA-192 (miR-192) has been demonstrated to be involved in diabetic retinopathy progression, to the best of our knowledge, its potential and mechanism in cell pyroptosis in diabetic retinopathy have not been studied. The present study demonstrated that high glucose (HG) contributes to the pyroptosis of retinal pigment epithelial (RPE) cells in a dose-dependent manner. The results revealed that miR-192 was weakly expressed in HG-induced RPE cells. Furthermore, overexpression of miR-192 abrogated the role of HG in RPE cell pyroptosis. Based on the bioinformatics analysis, a dual-luciferase reporter assay, and an RNA pull-down assay, FTO α-ketoglutarate-dependent dioxygenase (FTO) was demonstrated to be a direct target of miR-192. Additionally, upregulation of FTO abolished the effects of miR-192 on RPE cells treated with HG. Nucleotide-binding domain leucine-rich repeat family protein 3 (NLRP3) inflammasome activation is vital for cell pyroptosis, and FTO functions as a pivotal modulator in the N

Indexed as

Diabetic RetinopathyMicroRNAsAlpha-Ketoglutarate-Dependent Dioxygenase FTOEpithelial CellsGlucoseHumansInflammasomesNLR Family, Pyrin Domain-Containing 3 ProteinPyroptosisRetinal PigmentsAlpha-Ketoglutarate-Dependent Dioxygenase FTOFTO protein, humanGlucoseInflammasomesMicroRNAsMIRN192 microRNA, humanNLR Family, Pyrin Domain-Containing 3 ProteinRetinal Pigmentsdiabetic retinopathyftoMiR-192pyroptosisretinal pigment epithelial cell

Identifiers

PMID35441575
PMCPMC9161832
OpenAlexW4224231688

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.