Evidence map›Paper›PMID 37566944›Full record

ArticleRedox biology2023

Comparative mechanistic study of RPE cell death induced by different oxidative stresses.

Yao Tong, Yinga Wu, Jing Ma, Masataka Ikeda, Tomomi Ide, Courtney T Griffin, Xi-Qin Ding, Shusheng Wang

Open access · goldAbstract readComparative Study
In one paragraph

Article in Redox biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed
21.5field-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

47 citing papers in PubMed, 65 citations in OpenAlex.

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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 4 institutions in 2 countries.

Yao TongDepartment of Cell and Molecular Biology, Tulane University, New Orleans, LA, 70118, USA.
Yinga WuDepartment of Cell and Molecular Biology, Tulane University, New Orleans, LA, 70118, USA.
Jing MaDepartment of Cell and Molecular Biology, Tulane University, New Orleans, LA, 70118, USA.
Masataka IkedaDepartment of Cardiovascular Medicine, Faculty of Medical Sciences, Kyushu University, Fukuoka, Japan.
Tomomi IdeDepartment of Cardiovascular Medicine, Faculty of Medical Sciences, Kyushu University, Fukuoka, Japan.
Courtney T GriffinDepartment of Cell Biology, University of Oklahoma Health Sciences Center, Oklahoma City, OK, 73104, USA; Cardiovascular Biology Research Program, Oklahoma Medical Research Foundation, Oklahoma City, OK, USA.
Xi-Qin DingDepartment of Cell Biology, University of Oklahoma Health Sciences Center, Oklahoma City, OK, 73104, USA.
Shusheng WangDepartment of Cell and Molecular Biology, Tulane University, New Orleans, LA, 70118, USA; Department of Ophthalmology, Tulane University, New Orleans, LA, 70118, USA; Tulane Personalized Health Institute, Tulane University, New Orleans, LA, 70112, USA. Electronic address: swang1@tulane.edu.
Tulane University · USKyushu University · JPOklahoma Medical Research Foundation · USUniversity of Oklahoma Health Sciences Center · US

Funding

Scientific TransparencyP30EY001583 · NEI · UNIVERSITY OF PENNSYLVANIA · PI CLAIRE H MITCHELL · 1985 to 2026
$19.5M
Thyroid Hormone Signaling and Cone Photoreceptor DegenerationR01EY033841 · NEI · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI DING, XI-QIN · 2022 to 2025
$1.5M
NEI NIH HHS P30 EY001583NEI NIH HHS R01 EY033841
6 · The paper itself

Abstract

Oxidative stress is hypothesized to drive the progression of age-related macular degeneration (AMD). Retinal pigment epithelial (RPE) cell layer is important for supporting the function of retina and is particularly susceptible to oxidative stress-induced cell death. How RPE cells die in AMD, especially in geographic atrophy (GA), a late stage of dry AMD, is still controversial. The goal of this study is to compare the features and mechanisms of RPE cell death induced by different oxidative stresses, to identify potential universal therapeutic targets for GA. RPE cell death was induced both in vitro and ex vivo by 4-Hydroxynonenal (4-HNE), a major product of lipid peroxidation, sodium iodate (NaIO

Indexed as

FerroptosisMacular DegenerationCell DeathHumansLipidsOxidative StressReactive Oxygen SpeciesLipidsReactive Oxygen SpeciesAge-related macular degenerationex vivo modelFerroptosisGeographic atrophyNecroptosisOxidative stressRPE cell death

Identifiers

PMID37566944
PMCPMC10440584
OpenAlexW4385614427

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.