Evidence map›Paper›PMID 38261743›Full record

ArticleAging2024

IL-17 promotes IL-18 production via the MEK/ERK/miR-4492 axis in osteoarthritis synovial fibroblasts.

Kun-Tsan Lee, Chih-Yang Lin, Shan-Chi Liu, Xiu-Yuan He, Chun-Hao Tsai, Chih-Yuan Ko, Yuan-Hsin Tsai, Chia-Chia Chao, Po-Chun Chen, Chih-Hsin Tang

Open access · hybridAbstract 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 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
2.8field-weighted citation impact, top 11% 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

3 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
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

10 authors at 8 institutions in 1 country.

Kun-Tsan LeeDepartment of Post-Baccalaureate Medicine, National Chung-Hsing University, Taichung, Taiwan.
Chih-Yang LinTranslational Medicine Center, Shin-Kong Wu Ho-Su Memorial Hospital, Taipei City, Taiwan.
Shan-Chi LiuInstitute of Biomedical Sciences, Mackay Medical College, New Taipei City, Taiwan.
Xiu-Yuan HeDepartment of Pharmacology, School of Medicine, China Medical University, Taichung, Taiwan.
Chun-Hao TsaiDepartment of Orthopedic Surgery, China Medical University Hospital, Taichung, Taiwan.
Chih-Yuan KoDepartment of Orthopedic Surgery, China Medical University Hospital, Taichung, Taiwan.
Yuan-Hsin TsaiDepartment of Orthopedics, Show-Chwan Memorial Hospital, Changhua, Taiwan.
Chia-Chia ChaoDepartment of Respiratory Therapy, Fu-Jen Catholic University, New Taipei City, Taiwan.
Po-Chun ChenTranslational Medicine Center, Shin-Kong Wu Ho-Su Memorial Hospital, Taipei City, Taiwan.
Chih-Hsin TangDepartment of Pharmacology, School of Medicine, China Medical University, Taichung, Taiwan.
China Medical University Hospital · TWAsia University · TWChang Bing Show Chwan Memorial Hospital · TWChina Medical University · TWFu Jen Catholic University · TWMackay Medical College · TWNational Chung Hsing University · TWNational Taiwan Normal University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The concept of osteoarthritis (OA) as a low-grade inflammatory joint disorder has been widely accepted. Many inflammatory mediators are implicated in the pathogenesis of OA. Interleukin (IL)-18 is a pleiotropic cytokine with versatile cellular functions that are pathogenetically important in immune responses, as well as autoimmune, inflammatory, and infectious diseases. IL-17, a proinflammatory cytokine mainly secreted by Th17 cells, is upregulated in OA patients. However, the role of IL-17 in OA progression is unclear. The synovial tissues collected from healthy donors and OA patients were used to detect the expression level of IL-18 by IHC stain. The OA synovial fibroblasts (OASFs) were incubated with recombinant IL-17 and subjected to Western blot, qPCR, and ELISA to examine IL-18 expression level. The chemical inhibitors and siRNAs which targeted signal pathways were used to investigate signal pathways involved in IL-17-induced IL-18 expression. The microRNAs which participated IL-18 expression were surveyed with online databases miRWalk and miRDB, followed by validation with qPCR. This study revealed significantly higher levels of IL-18 expression in synovial tissue from OA patients compared with healthy controls, as well as increased IL-18 expression in OASFs from rats with severe OA.

Indexed as

MicroRNAsOsteoarthritisAnimalsCytokinesFibroblastsHumansInterleukin-17Interleukin-18Mitogen-Activated Protein Kinase KinasesRatsCytokinesInterleukin-17Interleukin-18MicroRNAsMitogen-Activated Protein Kinase KinasesIL-17IL-18osteoarthritis

Identifiers

PMID38261743
PMCPMC10866453
OpenAlexW4391104553

What OpenQuestion holds

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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.