Evidence map›Paper›PMID 35960381›Full record

ArticleJournal of bone and mineral metabolism2022

CD40/TRAF1 decreases synovial cell apoptosis in patients with rheumatoid arthritis through JNK/NF-κB pathway.

Tao Cheng, Jian Wu, Yaozeng Xu, Cuiping Liu, Huayong Zhang, Mingjun Wang

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In one paragraph

Article in Journal of bone and mineral metabolism, 2022. 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
0.6field-weighted citation impact, top 39% 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.

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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.

Tao Cheng *Department of Rheumatology, The First Affiliated Hospital of Soochow University, Suzhou, 215000, China. chengtao0526@126.com.
Jian Wu *Department of Rheumatology, The First Affiliated Hospital of Soochow University, Suzhou, 215000, China.
Yaozeng XuDepartment of Orthopedics, The First Affiliated Hospital of Soochow University, Suzhou, 215000, China.
Cuiping LiuDepartment of Rheumatology, The First Affiliated Hospital of Soochow University, Suzhou, 215000, China.
Huayong ZhangDepartment of Rheumatology and Immunology, The Affiliated Drum Tower Hospital, Medical School of Nanjing University, Nanjing, 210008, China.
Mingjun WangDepartment of Rheumatology, The First Affiliated Hospital of Soochow University, Suzhou, 215000, China. dlwmj@sina.com.
First Affiliated Hospital of Soochow University · CNSoochow University · CNNanjing Drum Tower Hospital · CN

Funding

Suzhou Minsheng science and technology project SYS2019043Suzhou Minsheng science and technology project SYS2020108
6 · The paper itself

Abstract

introductionA genome-wide association analysis revealed a rheumatoid arthritis (RA)-risk-associated genetic locus on chromosome 9, which contained the tumor necrosis factor receptor-associated factor 1 (TRAF1). However, the detail mechanism by TRAF1 signaled to fibroblast-like synoviocytes (FLSs) apoptosis remains to be fully understood. MATERIALS AND

methodsSynovial tissue of 10 RA patients and osteoarthritis patients were obtained during joint replacement surgery. We investigated TRAF1 level and FLSs apoptosis percentage in vivo and elucidated the mechanism involved in the regulation of apoptotic process in vitro.

resultsWe proved the significant increase of TRAF1 level in FLSs of RA patients and demonstrated that TRAF1 level correlated positively with DAS28 score and negatively with FLSs apoptosis. Treatment with siTRAF1 was able to decrease MMPs levels and the phosphorylated forms of JNK/NF-κB in vitro. Moreover, JNK inhibitor could attenuate expression of MMPs and increase percentage of apoptosis in RA-FLSs, while siTRAF1 could not promote apoptosis when RA-FLSs were pretreated with JNK activator.

conclusionsHigh levels of TRAF1 in RA synovium play an important role in the synovial hyperplasia of RA by suppressing apoptosis through activating JNK/NF-kB-dependent signaling pathways in response to the engagement of CD40.

Indexed as

Arthritis, RheumatoidSynoviocytesApoptosisCD40 AntigensCell ProliferationCells, CulturedFibroblastsGenome-Wide Association StudyHumansMAP Kinase Kinase 4NF-kappa BSynovial MembraneTNF Receptor-Associated Factor 1CD40 AntigensMAP Kinase Kinase 4NF-kappa BTNF Receptor-Associated Factor 1ApoptosisJNK/NF-κBRheumatoid arthritisTRAF1

Identifiers

PMID35960381
OpenAlexW4291145270

What OpenQuestion holds

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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.