Evidence map›Paper›PMID 39594655›Full record

ArticleCells2024

Thrombospondin 1 Mediates Autophagy Upon Inhibition of the Rho-Associated Protein Kinase Inhibitor.

Kirk Patrick Carreon Catral, Choi-Yee Tse, Wei-Ying Yang, Choi-Ying Ling, Oi-Lam Kwok, Kit-Ying Choy, Da-Qian Lu, Jing-Fang Bian, Thomas Chuen Lam, Dennis Yan-Yin Tse and 1 more

Abstract read
In one paragraph

Article in Cells, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. 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.

Kirk Patrick Carreon CatralSchool of Optometry, The Hong Kong Polytechnic University, Hong Kong, China.ORCID 0000-0001-6458-4875
Choi-Yee TseSchool of Optometry, The Hong Kong Polytechnic University, Hong Kong, China.
Wei-Ying YangSchool of Optometry, The Hong Kong Polytechnic University, Hong Kong, China.ORCID 0009-0008-1392-3011
Choi-Ying LingSchool of Optometry, The Hong Kong Polytechnic University, Hong Kong, China.ORCID 0009-0006-4472-3202
Oi-Lam KwokSchool of Optometry, The Hong Kong Polytechnic University, Hong Kong, China.
Kit-Ying ChoySchool of Optometry, The Hong Kong Polytechnic University, Hong Kong, China.ORCID 0000-0001-8696-4246
Da-Qian LuSchool of Optometry, The Hong Kong Polytechnic University, Hong Kong, China.ORCID 0000-0003-2804-2424
Jing-Fang BianSchool of Optometry, The Hong Kong Polytechnic University, Hong Kong, China.ORCID 0000-0003-0464-1705
Thomas Chuen LamSchool of Optometry, The Hong Kong Polytechnic University, Hong Kong, China.ORCID 0000-0002-3511-5620
Dennis Yan-Yin TseSchool of Optometry, The Hong Kong Polytechnic University, Hong Kong, China.ORCID 0000-0001-7561-9121
Samantha Sze-Wan ShanSchool of Optometry, The Hong Kong Polytechnic University, Hong Kong, China.ORCID 0000-0001-6876-9914

Funding

Health and Medical Research Fund 08191556Health and Medical Research Fund 09200276Hong Kong Polytechnic University 1-BBDLHong Kong Polytechnic University 1-BD6RHong Kong Polytechnic University PolyU Research Postgraduate StudentshipResearch Centre for SHARP Vision 1-BBC0Research Centre for SHARP Vision 1-BBDAThe InnoHK initiative of the Hong Kong Special Administrative Region Government The InnoHK initiative of the Hong Kong Special Administrative Region GovernmentUniversity Grants Committee (UGC) U-ZEZ2
6 · The paper itself

Abstract

Age-related macular degeneration (AMD) is a degenerative eye disease leading to central vision loss and is characterized by dysregulated autophagy of the retinal pigment epithelium (RPE) layer. Recent studies have suggested that rho-associated protein kinase (ROCK) inhibitors may enhance autophagy in neurodegenerative diseases and promote the survival of RPE cells. This study investigated the effect of ROCK inhibitors on autophagy gene expression and autophagic vacuole formation in a human RPE (ARPE-19) cell line. The highly selective and potent ROCK inhibitor Y-39983 enhanced the expression of autophagy genes in ARPE-19 cells and increased autophagic vacuole formation. A proteomic analysis using mass spectrometry was performed to further characterize the effects of ROCK inhibition at the protein level. Y-39983 downregulated thrombospondin-1 (THBS1), and suppression of THBS1 in ARPE-19 cells resulted in an increase in autophagic vacuole formation. Our data showed that ROCK inhibitor-induced autophagy was mediated by THBS1 downregulation. We identified ROCK and THBS1 as potential novel therapeutic targets in AMD.

Indexed as

AutophagyProtein Kinase InhibitorsRetinal Pigment Epitheliumrho-Associated KinasesThrombospondin 1Cell LineDown-RegulationHumansVacuolesProtein Kinase Inhibitorsrho-Associated KinasesThrombospondin 1thrombospondin-1, humanAMDautophagyROCK inhibitorsignaling pathwayThrombospondin-1

Identifiers

PMID39594655
PMCPMC11593289

What Socratic 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 Socratic graph.