Evidence map›Paper›PMID 34158084›Full record

ArticleJournal of orthopaedic surgery and research2021

T-614 attenuates knee osteoarthritis via regulating Wnt/β-catenin signaling pathway.

Shan Cong, Yan Meng, Lingrui Wang, Jiao Sun, Ta Bu Shi Nu Er Xia Ti, Li Luo

Open access · goldAbstract read
In one paragraph

Article in Journal of orthopaedic surgery and research, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 1 pooled it
1.9field-weighted citation impact, top 15% 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

9 citing papers in PubMed, 1 synthesis or guideline pooled it, 15 citations in OpenAlex.

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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

6 authors at 3 institutions in 1 country.

Shan CongDepartment of Rheumatism and Immunology, First Affiliated Hospital of Xinjiang Medical University, Xinjiang, 830017, P.R. China.
Yan MengDepartment of Rheumatism and Immunology, First Affiliated Hospital of Xinjiang Medical University, Xinjiang, 830017, P.R. China.
Lingrui WangDepartment of Rheumatism and Immunology, Xinjiang Medical University, Xinjiang, 830017, P.R. China.
Jiao SunDepartment of Rheumatism and Immunology, First Affiliated Hospital of Xinjiang Medical University, Xinjiang, 830017, P.R. China.
Ta Bu Shi Nu Er Xia TiDepartment of Rheumatism and Immunology, The Second Affiliated Hospital of Xinjiang Medical University, Xinjiang, 830017, P.R. China.
Li LuoDepartment of Rheumatism and Immunology, First Affiliated Hospital of Xinjiang Medical University, Xinjiang, 830017, P.R. China. luoliwork88@163.com.
Xinjiang Medical University · CNFirst Affiliated Hospital of Xinjiang Medical University · CNSecond Affiliated Hospital of Xinjiang Medical University · CN

Funding

Simcere Special Scientific Research Fund KY2579.03
6 · The paper itself

Abstract

backgroundThe aim of this study was to investigate the effect of Iguratimod (T-614) on rat knee osteoarthritis (KOA) and further to explore its underlying mechanism.

methodsIn this study, papain-induced KOA model was constructed. Hematoxylin and eosin (H&E) staining was conducted to observe the pathological changes of cartilage tissue and Mankin scoring principle was used for quantitative scoring. Transmission electron microscopy (TEM) was applied to observe the ultrastructure of cartilage tissue. ELISA was used to measure the levels of matrix metalloproteinase 13 (MMP-13) and inflammatory factors (interleukin (IL)-6 and tumor necrosis factor a (TNF-a)) in serum. RT-qPCR and immunohistochemistry were conducted to detect mRNA expression and protein expression of key genes in Wnt/β-catenin pathway.

resultsH&E, Mankin scoring, and TEM data confirmed that compared with model group, T-614 significantly improved the degeneration of articular cartilage. Besides, we observed that low, middle, and high doses of T-614 could decrease the levels of MMP13, TNF-α, and IL-6 in serum to different degrees. Mechanically, T-614 downregulated the mRNA and protein expression of β-catenin and MMP13 in cartilage tissue via a dose-dependent manner, and on the contrary upregulated the mRNA and protein expression of glucogen synthase kinase-3 beta (GSK-3β).

conclusionOur results suggested that T-614 can reduce the level of its downstream target gene MMP-13 and downregulate the expression of inflammatory cytokines TNF-α and IL-6 by regulating the Wnt/β-catenin signaling pathway, thereby inhibiting joint inflammation and controlling KOA degeneration of articular cartilage.

Indexed as

AnimalsBenzopyransbeta CateninCartilage, ArticularChromonesDisease Models, AnimalDose-Response Relationship, DrugDown-RegulationGlycogen Synthase Kinase 3 betaInterleukin-6Matrix Metalloproteinase 13Osteoarthritis, KneePapainRatsSulfonamidesTumor Necrosis Factor-alphaBenzopyransbeta CateninChromonesGlycogen Synthase Kinase 3 betaiguratimodInterleukin-6Matrix Metalloproteinase 13Mmp13 protein, ratPapainSulfonamidesT 614Tumor Necrosis Factor-alphaArticular cartilageIguratimodInflammationKnee osteoarthritisWnt/β-catenin signaling pathway

Identifiers

PMID34158084
PMCPMC8220752
OpenAlexW3177170253

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.