Evidence map›Paper›PMID 38683123›Full record

ArticleAging2024

Senescent characteristics of human corneal endothelial cells upon ultraviolet-A exposure.

Kohsaku Numa, Sandip Kumar Patel, Zhixin A Zhang, Jordan B Burton, Akifumi Matsumoto, Jun-Wei B Hughes, Chie Sotozono, Birgit Schilling, Pierre-Yves Desprez, Judith Campisi and 1 more

Abstract read
In one paragraph

Article in Aging, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Integrative Approaches to Treating Cellular Senescence in Kidney Disease.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Review
  4. 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

11 authors.

Kohsaku NumaBuck Institute for Research on Aging, Novato, CA 94945, USA.
Sandip Kumar PatelBuck Institute for Research on Aging, Novato, CA 94945, USA.
Zhixin A ZhangBuck Institute for Research on Aging, Novato, CA 94945, USA.
Jordan B BurtonBuck Institute for Research on Aging, Novato, CA 94945, USA.
Akifumi MatsumotoKyoto Prefectural University of Medicine, Department of Ophthalmology, Kyoto 6020841, Japan.
Jun-Wei B HughesBuck Institute for Research on Aging, Novato, CA 94945, USA.
Chie SotozonoKyoto Prefectural University of Medicine, Department of Ophthalmology, Kyoto 6020841, Japan.
Birgit SchillingBuck Institute for Research on Aging, Novato, CA 94945, USA.
Pierre-Yves DesprezBuck Institute for Research on Aging, Novato, CA 94945, USA.
Judith CampisiBuck Institute for Research on Aging, Novato, CA 94945, USA.
Koji KitazawaBuck Institute for Research on Aging, Novato, CA 94945, USA.

Funding

THE IMPACT OF CELLULAR DEFENSE ON THE ROLE OF Ku80 IN GENOME MAINTENANCE AND LONGP01AG017242 · NIA · UNIVERSITY OF TEXAS HLTH SCI CTR SAN ANT · PI VIJG, JAN · 1999 to 2023
$46.1M
Single cell analysis coreP01AG066591 · NIA · BUCK INSTITUTE FOR RESEARCH ON AGING · PI MELOV, SIMON · 2021 to 2025
$15.5M
CELLULAR SENESCENCE AND CONTROL OF GENE EXPRESSIONR37AG009909 · NIA · UNIVERSITY OF CALIF-LAWRENC BERKELEY LAB · PI CAMPISI, JUDITH · 1995 to 2015
$7.6M
USC Geroscience Training in the Biology of AgingT32AG052374 · NIA · UNIVERSITY OF SOUTHERN CALIFORNIA · PI Sean P CURRAN · 2016 to 2026
$5.3M
Quantitative Proteomics to Develop Robust Senescence-Related Biomarkers for AgingU01AG060906 · NIA · BUCK INSTITUTE FOR RESEARCH ON AGING · PI SCHILLING, BIRGIT · 2018 to 2022
$4.0M
Cellular senescence and control of gene expressionR56AG009909 · NIA · BUCK INSTITUTE FOR RESEARCH ON AGING · PI CAMPISI, JUDITH · 2017 to 2017
$592k
NIA NIH HHS P01 AG017242NIA NIH HHS P01 AG066591NIA NIH HHS R37 AG009909NIA NIH HHS R56 AG009909NIA NIH HHS T32 AG052374NIA NIH HHS U01 AG060906
6 · The paper itself

Abstract

purposeThe objective of this study was to investigate the senescent phenotypes of human corneal endothelial cells (hCEnCs) upon treatment with ultraviolet (UV)-A.

methodsWe assessed cell morphology, senescence-associated β-galactosidase (SA-β-gal) activity, cell proliferation and expression of senescence markers (

resultsCells exposed to 5 J/cm2 of UV-A or to IR exhibited typical senescent phenotypes, including enlargement, increased SA-β-gal activity, decreased cell proliferation and elevated expression of

conclusionsIn this study, where senescence was induced by UV-A, a more physiological stress for hCEnCs compared to IR, we determined that UV-A modulated the expression of many genes and proteins typically altered upon IR treatment, a more conventional method of senescence induction, even though UV-A also modulated specific pathways unrelated to IR.

Indexed as

Cell ProliferationCellular SenescenceEndothelial CellsUltraviolet Raysbeta-GalactosidaseCells, CulturedCyclin-Dependent Kinase Inhibitor p16Cyclin-Dependent Kinase Inhibitor p21Endothelium, CornealHumansProteomicsbeta-GalactosidaseCyclin-Dependent Kinase Inhibitor p16Cyclin-Dependent Kinase Inhibitor p21cellular senescencegene ontology analysisproteomicsRNA-Seqsenescence-associated secretory phenotype

Identifiers

PMID38683123
PMCPMC11087119

What OpenQuestion holds

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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.