Evidence map›Paper›PMID 34839589›Full record

ArticleJournal of diabetes investigation2022

CircZNF532 knockdown protects retinal pigment epithelial cells against high glucose-induced apoptosis and pyroptosis by regulating the miR-20b-5p/STAT3 axis.

Gao-Hua Liang, Yan-Ni Luo, Ri-Zhang Wei, Jia-Yang Yin, Zhi-Liang Qin, Li-Li Lu, Wen-Hao Ma

Open access · goldAbstract read
In one paragraph

Article in Journal of diabetes investigation, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
2.3field-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

24 citing papers in PubMed, 32 citations in OpenAlex.

  1. Article
  2. MALAT1-miR-20b-5p-P2RX7 Axis RegulatesVeterinary sciences · 2026
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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

7 authors at 2 institutions in 1 country.

Gao-Hua LiangDepartment of Ophthalmology, The Affiliated Hospital of Youjiang Medical University for Nationalities, Baise, China.
Yan-Ni LuoDepartment of Ophthalmology, The Affiliated Hospital of Youjiang Medical University for Nationalities, Baise, China.
Ri-Zhang WeiDepartment of Ophthalmology, The Affiliated Hospital of Youjiang Medical University for Nationalities, Baise, China.
Jia-Yang YinDepartment of Ophthalmology, The First Affiliated Hospital of Jinan University, Guangzhou, China.
Zhi-Liang QinDepartment of Ophthalmology, The Affiliated Hospital of Youjiang Medical University for Nationalities, Baise, China.
Li-Li LuDepartment of Ophthalmology, The Affiliated Hospital of Youjiang Medical University for Nationalities, Baise, China.
Wen-Hao MaDepartment of Ophthalmology, The Affiliated Hospital of Youjiang Medical University for Nationalities, Baise, China.ORCID https://orcid.org/0000-0002-7601-2337
Affiliated Hospital of Youjiang Medical University for Nationalities · CNFirst Affiliated Hospital of Jinan University · CN

Funding

Natural Science Foundation of Guangxi 2020GXNSFAA259054The First Batch of High-level Talent Scientific Research Projects of the Affiliated Hospital of Youjiang Medical University for Nationalities in 2019 R20196340The First Batch of High-level Talent Scientific Research Projects of the Affiliated Hospital of Youjiang Medical University for Nationalities in 2019 Y20196304
6 · The paper itself

Abstract

introductionThe loss of retinal pigment epithelial (RPE) cells is associated with the etiology of diabetic retinopathy (DR). This study investigated the effects of circular RNA ZNF532 (circZNF532) on apoptosis and pyroptosis of RPE cells. MATERIALS AND

methodsBlood samples were collected from patients with DR and healthy volunteers. A human RPE cell line ARPE-19 was induced by high glucose (HG) and assayed for cell viability, apoptosis, and pyroptosis. The binding of miR-20b-5p with circZNF532 and STAT3 was confirmed by a luciferase activity assay. A mouse model of diabetic retinopathy was established.

resultsCircZNF532 and STAT3 were upregulated but miR-20b-5p was downregulated in the serum samples of patients with DR and HG-induced ARPE-19 cells. Elevated miR-20b-5p or CircZNF532 knockdown enhanced proliferation but reduced apoptosis and pyroptosis of ARPE-19 cells. CircZNF532 sponged miR-20b-5p and inhibited its expression. STAT3 was verified as a target of miR-20b-5p. MiR-20b-5p modulated ARPE-19 cell viability, apoptosis, and pyroptosis by targeting STAT3. Mice with STZ-induced diabetes showed elevated expressions of circZNF532 and STAT3 but decreased the level of miR-20b-5p compared with the controls. Knockdown of circZNF532 inhibited apoptosis and pyroptosis in mouse retinal tissues.

conclusionCircZNF532 knockdown rescued human RPE cells from HG-induced apoptosis and pyroptosis by regulating STAT3 via miR-20b-5p.

Indexed as

Diabetic RetinopathyMicroRNAsRetinal Pigment EpitheliumRNA, CircularSTAT3 Transcription FactorAnimalsApoptosisEpithelial CellsGlucoseHumansMicePyroptosisGlucoseMicroRNAsMIRN20b microRNA, humanRNA, CircularSTAT3 protein, humanSTAT3 Transcription FactorDiabetic retinopathymiR-20b-5pSTAT3

Identifiers

PMID34839589
PMCPMC9077727
OpenAlexW3216465827

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.