Evidence map›Paper›PMID 38849923›Full record

ArticleAdvances in rheumatology (London, England)2024

TAK-242 (Resatorvid) inhibits proinflammatory cytokine production through the inhibition of NF-κB signaling pathway in fibroblast-like synoviocytes in osteoarthritis patients.

Mohammadreza Khomeijani-Farahani, Jafar Karami, Elham Farhadi, Samaneh Soltani, Ali-Akbar Delbandi, Mehdi Shekarabi, Mohammad Naghi Tahmasebi, Arash Sharafat Vaziri, Ahmadreza Jamshidi, Mahdi Mahmoudi and 1 more

Abstract read
In one paragraph

Article in Advances in rheumatology (London, England), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

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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

11 authors.

Mohammadreza Khomeijani-FarahaniRheumatology Research Center, Tehran University of Medical Sciences, Tehran, Iran.
Jafar KaramiRheumatology Research Center, Tehran University of Medical Sciences, Tehran, Iran.
Elham FarhadiRheumatology Research Center, Tehran University of Medical Sciences, Tehran, Iran.
Samaneh SoltaniRheumatology Research Center, Tehran University of Medical Sciences, Tehran, Iran.
Ali-Akbar DelbandiDepartment of Immunology, School of Medicine, Iran University of Medical Sciences, Tehran, Iran.
Mehdi ShekarabiDepartment of Immunology, School of Medicine, Iran University of Medical Sciences, Tehran, Iran. shekarabi.m@iums.ac.ir.
Mohammad Naghi TahmasebiDepartment of Orthopedics, Division of Knee Surgery, Shariati Hospital, Tehran University of Medical Sciences, Tehran, Iran.
Arash Sharafat VaziriDepartment of Orthopedics, Division of Knee Surgery, Shariati Hospital, Tehran University of Medical Sciences, Tehran, Iran.
Ahmadreza JamshidiRheumatology Research Center, Tehran University of Medical Sciences, Tehran, Iran.
Mahdi MahmoudiRheumatology Research Center, Tehran University of Medical Sciences, Tehran, Iran. mahmoudim@tums.ac.ir.ORCID 0000-0002-8164-8831
Masoomeh AkhlaghiRheumatology Research Center, Tehran University of Medical Sciences, Tehran, Iran. makhlaghi@tums.ac.ir.

Funding

Tehran University of Medical Sciences and Health Services 97-01-41-38251
6 · The paper itself

Abstract

backgroundFibroblast-like synoviocytes (FLSs) are involved in osteoarthritis (OA) pathogenesis through pro-inflammatory cytokine production. TAK-242, a TLR4 blocker, has been found to have a significant impact on the gene expression profile of pro-inflammatory cytokines such as IL1-β, IL-6, TNF-α, and TLR4, as well as the phosphorylation of Ikβα, a regulator of the NF-κB signaling pathway, in OA-FLSs. This study aims to investigate this effect because TLR4 plays a crucial role in inflammatory responses. MATERIALS AND

methodsTen OA patients' synovial tissues were acquired, and isolated FLSs were cultured in DMEM in order to assess the effectiveness of TAK-242. The treated FLSs with TAK-242 and Lipopolysaccharides (LPS) were analyzed for the mRNA expression level of IL1-β, IL-6, TNF-α, and TLR4 levels by Real-Time PCR. Besides, we used western blot to assess the protein levels of Ikβα and pIkβα.

resultsThe results represented that TAK-242 effectively suppressed the gene expression of inflammatory cytokines IL1-β, IL-6, TNF-α, and TLR4 which were overexpressed upon LPS treatment. Additionally, TAK-242 inhibited the phosphorylation of Ikβα which was increased by LPS treatment.

conclusionAccording to our results, TAK-242 shows promising inhibitory effects on TLR4-mediated inflammatory responses in OA-FLSs by targeting the NF-κB pathway. TLR4 inhibitors, such as TAK-242, may be useful therapeutic agents to reduce inflammation and its associated complications in OA patients, since traditional and biological treatments may not be adequate for all of them.

Indexed as

CytokinesInterleukin-1betaInterleukin-6LipopolysaccharidesNF-kappa BSignal TransductionSulfonamidesSynoviocytesToll-Like Receptor 4Tumor Necrosis Factor-alphaCells, CulturedFemaleFibroblastsHumansMaleMiddle AgedCytokinesethyl 6-(N-(2-chloro-4-fluorophenyl)sulfamoyl)cyclohex-1-ene-1-carboxylateIL1B protein, humanIL6 protein, humanInterleukin-1betaInterleukin-6LipopolysaccharidesNF-kappa BRNA, MessengerSulfonamidesTLR4 protein, humanToll-Like Receptor 4Tumor Necrosis Factor-alphaFibroblast-like synoviocytesIL1-βIL-6OsteoarthritisTAK-242TLR4TNF-α

Identifiers

PMID38849923
PMCPMC13488737

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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.