Evidence map›Paper›PMID 37391574›Full record

ReviewCellular and molecular neurobiology2023

Oxidative Stress-Involved Mitophagy of Retinal Pigment Epithelium and Retinal Degenerative Diseases.

Si-Ming Zhang, Bin Fan, Yu- Lin Li, Zhao-Yang Zuo, Guang-Yu Li

Open access · hybridAbstract readReview
In one paragraph

Review in Cellular and molecular neurobiology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 58 papers.

0numbers the graph read from it
0cells of the map it votes in
58citing papers in PubMed
22.6field-weighted citation impact, top 1% 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

58 citing papers in PubMed, 81 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Review
  6. Review
  7. Article
  8. Review
  9. Spontaneous whole retinal degeneration in aged Beclin1 heterozygous mice.Journal of neural transmission (Vienna, Austria : 1996) · 2026
    Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Review
  16. Review
  17. Article
  18. Article
  19. 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

5 authors at 2 institutions in 1 country.

Si-Ming ZhangDepartment of Ophthalmology, Second Norman Bethune Hospital of Jilin University, Changchun, 130000, China.ORCID https://orcid.org/0000-0003-0836-6077
Bin FanDepartment of Ophthalmology, Second Norman Bethune Hospital of Jilin University, Changchun, 130000, China.ORCID https://orcid.org/0000-0003-0641-1129
Yu- Lin LiDepartment of Ophthalmology, Second Norman Bethune Hospital of Jilin University, Changchun, 130000, China.ORCID https://orcid.org/0000-0002-6337-3782
Zhao-Yang ZuoDepartment of Ophthalmology, Second Norman Bethune Hospital of Jilin University, Changchun, 130000, China.ORCID https://orcid.org/0000-0002-7021-7358
Guang-Yu LiDepartment of Ophthalmology, Second Norman Bethune Hospital of Jilin University, Changchun, 130000, China. liguangyu@aliyun.com.ORCID https://orcid.org/0000-0002-6338-2507
First Bethune Hospital of Jilin University · CNJilin University · CN

Funding

National Natural Science Foundation of China 82171053Natural Science Foundation of Jilin Province 20200801043GH
6 · The paper itself

Abstract

The retinal pigment epithelium (RPE) is a highly specialized and polarized epithelial cell layer that plays an important role in sustaining the structural and functional integrity of photoreceptors. However, the death of RPE is a common pathological feature in various retinal diseases, especially in age-related macular degeneration (AMD) and diabetic retinopathy (DR). Mitophagy, as a programmed self-degradation of dysfunctional mitochondria, is crucial for maintaining cellular homeostasis and cell survival under stress. RPE contains a high density of mitochondria necessary for it to meet energy demands, so severe stimuli can cause mitochondrial dysfunction and the excess generation of intracellular reactive oxygen species (ROS), which can further trigger oxidative stress-involved mitophagy. In this review, we summarize the classical pathways of oxidative stress-involved mitophagy in RPE and investigate its role in the progression of retinal diseases, aiming to provide a new therapeutic strategy for treating retinal degenerative diseases. The role of mitophagy in AMD and DR. In AMD, excessive ROS production promotes mitophagy in the RPE by activating the Nrf2/p62 pathway, while in DR, ROS may suppress mitophagy by the FOXO3-PINK1/parkin signaling pathway or the TXNIP-mitochondria-lysosome-mediated mitophagy.

Indexed as

Macular DegenerationRetinal Pigment EpitheliumHumansMitophagyOxidative StressReactive Oxygen SpeciesReactive Oxygen SpeciesAge-related macular degenerationDiabetic retinopathyMitophagyOxidative stressRetinal pigment epithelium

Identifiers

PMID37391574
PMCPMC10477140
OpenAlexW4382651679

What OpenQuestion holds

Textmetadata
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.