Evidence map›Paper›PMID 32051471›Full record

ArticleScientific reports2020

DJ-1 protects retinal pericytes against high glucose-induced oxidative stress through the Nrf2 signaling pathway.

Wanpeng Wang, Han Zhao, Baihua Chen

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
3.3field-weighted citation impact, top 8% 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

31 citing papers in PubMed, 55 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Review
  7. DJ-1 Serves as a Central Regulator of Diabetes Complications.Current issues in molecular biology · 2025
    Review
  8. Article
  9. Article
  10. The Role of Nutrition Across Production Stages to Improve Sow Longevity.Animals : an open access journal from MDPI · 2025
    Review
  11. Review
  12. Review
  13. Article
  14. Article
  15. Article
  16. Resilience to diabetic retinopathy.Progress in retinal and eye research · 2024
    Review
  17. Article
  18. Article
  19. Frontiers in endocrinology · 2023
    Article
  20. Article
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

3 authors at 3 institutions in 1 country.

Wanpeng WangDepartment of Ophthalmology, the second Xiangya Hospital of Central South University, Changsha, Hunan, 410011, China.
Han ZhaoDepartment of Ophthalmology, the second Xiangya Hospital of Central South University, Changsha, Hunan, 410011, China.
Baihua ChenDepartment of Ophthalmology, the second Xiangya Hospital of Central South University, Changsha, Hunan, 410011, China. chenbaihua2017@csu.edu.cn.
Central South University · CNHunan Provincial Center for Disease Control and Prevention · CNXiangya Hospital Central South University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Oxidative stress has been associated with the etipathogenesis of Diabetic retinopathy (DR). Studies have shown that DJ-1 plays an important role in regulating the reactive oxygen species (ROS) production and resistance to oxidative stress-induced apoptosis. This study aimed to investigate whether DJ-1 upregulates oxidative stress and prevents damage to retinal capillary pericytes by increasing antioxidant capacity through the Nuclear factor erythroid 2-related factor 2 (Nrf2) signaling pathway. Nrf2 is a redox-sensitive transcription factor that encode antioxidant enzymes and phase II metabolic enzymes, activation of Nrf2 functions is one of the critical defensive mechanisms against oxidative stress in many tissues. Our results showed after DJ-1 overexpression, apoptosis of rat retinal pericytes (RRPs) decreased, the ratio of B-cell lymphoma-2 (Bcl-2) to BCL2-Associated X Protein (BAX) increased, the production of ROS decreased, and the protein expression and activity of manganese superoxide dismutase (MnSOD, also called SOD2) and catalase (CAT) increased. DJ-1 overexpression activated Nrf2 expression, however, after Nrf2 silencing, apoptosis of RRPs increased, the ratio of Bcl-2 to BAX decreased, the production of ROS increased, the protein expression of MnSOD and CAT decreased, and the expression of heme oxygenase-1 (HO-1), NADP(H) quinone oxidoreductase (NQO1), glutamate-cysteine ligase catalytic subunit (GCLC) and modifier subunit (GCLM) decreased. These data suggest that enhancement of the Nrf2 pathway is a potential protective strategy for the treatment of DR. Therefore, DJ-1 may prevent high glucose-induced oxidative stress and RRPs apoptosis through the Nrf2 signaling pathway, thereby preventing the early onset and progression of DR.

Indexed as

Oxidative StressAnimalsApoptosisbcl-2-Associated X ProteinCatalaseCells, CulturedDiabetic RetinopathyGlucoseHeme Oxygenase-1NADPNAD(P)H Dehydrogenase (Quinone)NF-E2-Related Factor 2PericytesProtein Deglycase DJ-1Proto-Oncogene Proteins c-bcl-2RatsBax protein, ratbcl-2-Associated X ProteinCatalaseGlucoseHeme Oxygenase-1NADPNAD(P)H Dehydrogenase (Quinone)NF-E2-Related Factor 2NQO1 protein, ratPARK7 protein, ratProtein Deglycase DJ-1Proto-Oncogene Proteins c-bcl-2Superoxide DismutaseSuperoxide Dismutase 2

Identifiers

PMID32051471
PMCPMC7016111
OpenAlexW3005564435

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.