Evidence map›Paper›PMID 23861949›Full record

ArticlePloS one2013

Celastrol inhibits lipopolysaccharide-stimulated rheumatoid fibroblast-like synoviocyte invasion through suppression of TLR4/NF-κB-mediated matrix metalloproteinase-9 expression.

Guoqing Li, Dan Liu, Yu Zhang, Yayun Qian, Hua Zhang, Shiyu Guo, Masataka Sunagawa, Tadashi Hisamitsu, Yanqing Liu

RetractedOpen access · goldAbstract readRetracted Publication
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It has been retracted, and should not be counted. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
7.1field-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

45 citing papers in PubMed, 91 citations in OpenAlex.

  1. Trial
  2. Article
  3. The role of celastrol in inflammation and diseases.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2025
    Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Qiguiyin Decoction Improves Multidrug-ResistantBioMed research international · 2022
    Article
  9. Review
  10. Article
  11. Article
  12. Frontiers in pharmacology · 2021
    Review
  13. Article
  14. Deciphering the Active Ingredients and Molecular Mechanisms ofEvidence-based complementary and alternative medicine : eCAM · 2020
    Article
  15. Review
  16. Review
  17. Article
  18. Review
  19. CaBritish journal of pharmacology · 2019
    Article
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 2 institutions in 2 countries.

Guoqing LiDepartment of Rheumatology, Clinical Medical College, Yangzhou University, Yangzhou, Jiangsu, China.
Dan Liu
Yu Zhang
Yayun Qian
Hua Zhang
Shiyu Guo
Masataka Sunagawa
Tadashi Hisamitsu
Yanqing Liu
Yangzhou University · CNShowa University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Invasion of fibroblast-like synoviocytes (FLSs) is critical in the pathogenesis of rheumatoid arthritis (RA). The metalloproteinases (MMPs) and activator of Toll-like receptor 4 (TLR4)/nuclear factor-κB (NF-κB) pathway play a critical role in RA-FLS invasion induced by lipopolysaccharide (LPS). The present study aimed to explore the anti-invasive activity of celastrol on LPS-stimulated human RA-FLSs, and to elucidate the mechanism involved. We investigated the effect of celastrol on LPS-induced FLS migration and invasion as well as MMP expression and explored the upstream signal transduction. Results showed that celastrol suppressed LPS-stimulated FLS migration and invasion by inhibiting MMP-9 expression and activity. Furthermore, our results revealed that celastrol inhibited the transcriptional activity of MMP-9 by suppressing the binding activity of NF-κB in the MMP-9 promoter, and suppressed the TLR4/MyD88/NF-κB pathway. Administration of celastrol (0.5 mg/kg and 1 mg/kg, intraperitoneally) daily for 3 weeks in a collagen-induced arthritis rat model markedly alleviated the clinical signs, synovial hyperplasia and inflammatory cell infiltration of joints. In conclusion, celastrol might inhibit FLS migration and invasion induced by LPS by suppressing TLR4/NF-κB-mediated MMP-9 expression, providing a theoretical foundation for the clinical treatment of RA with celastrol.

Indexed as

AnimalsAnti-Inflammatory Agents, Non-SteroidalArthritis, ExperimentalArthritis, RheumatoidCell CycleCell MovementCell SurvivalCollagen Type IIFemaleGene Expression RegulationHumansJoint CapsuleLipopolysaccharidesMatrix Metalloproteinase 9NF-kappa BPentacyclic TriterpenesAnti-Inflammatory Agents, Non-SteroidalcelastrolCollagen Type IILipopolysaccharidesMatrix Metalloproteinase 9NF-kappa BPentacyclic TriterpenesTlr4 protein, ratToll-Like Receptor 4Triterpenes

Identifiers

PMID23861949
PMCPMC3701694
OpenAlexW2061730145

What OpenQuestion 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 OpenQuestion graph.