Evidence map›Paper›PMID 36899378›Full record

ArticleJournal of orthopaedic surgery and research2023

Specificity protein 1-mediated ACSL4 transcription promoted the osteoarthritis progression through suppressing the ferroptosis of chondrocytes.

Wen He, Xuchao Lin, Kangyao Chen

Open access · goldFull text read
In one paragraph

Article in Journal of orthopaedic surgery and research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
6.9field-weighted citation impact, top 3% 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

21 citing papers in PubMed, 29 citations in OpenAlex.

  1. Regulation of ferroptosis by BAP1.Cell death and differentiation · 2026
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  14. Ferroptosis in Arthritis: Driver of the Disease or Therapeutic Option?International journal of molecular sciences · 2024
    Review
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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

3 authors at 1 institution in 1 country.

Wen He *Department of Orthopaedics, Fuzhou Second Hospital, No. 47, Shangteng Road, Cangshan District, Fuzhou City, 350007, Fujian Province, China. 93864669@qq.com.
Xuchao Lin *Department of Orthopaedics, Fuzhou Second Hospital, No. 47, Shangteng Road, Cangshan District, Fuzhou City, 350007, Fujian Province, China.
Kangyao ChenDepartment of Orthopaedics, Fuzhou Second Hospital, No. 47, Shangteng Road, Cangshan District, Fuzhou City, 350007, Fujian Province, China.
Fuzhou Second Hospital · CN

Funding

Fujian Provincial Clinical Medical Research Center for First Aid and Rehabilitation in Orthopaedic Trauma 2020Y2014Fuzhou Trauma Medical Center 2018080303
6 · The paper itself

Abstract

backgroundChondrocytes are the main cell damage type involved in the occurrence and development of osteoarthritis (OA). Ferroptosis has been confirmed to be related to many degenerative diseases. This research aimed to explore the role of Sp1 and ACSL4 in ferroptosis in the IL-1β-treated human chondrocyte cells line (HCCs).

methodsThe cell viability was detected with CCK8 assay. The ROS, MDA, GSH, and Fe

resultsThe results showed that IL-1β stimulation elevated the LDH release, cell viability, ROS, MDA and Fe

conclusionUpregulation of Sp1 activates Ascl4 transcription and thus mediates the occurrence of ferroptosis. Hence, Acsl4 may be a therapeutic target for intervention of OA.

Indexed as

Coenzyme A LigasesFerroptosisOsteoarthritisSp1 Transcription FactorChondrocytesHumansMatrix Metalloproteinase 13Reactive Oxygen SpeciesCoenzyme A LigasesMatrix Metalloproteinase 13Reactive Oxygen SpeciesSP1 protein, humanSp1 Transcription FactorAcsl4FerroptosisOsteoarthritisSp1

Identifiers

PMID36899378
PMCPMC10007726
OpenAlexW4323864305

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Textfull text, public
LicenceCC BY
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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.