Evidence map›Paper›PMID 26823778›Full record

ArticleInternational journal of clinical and experimental pathology2015

MiR-451 inhibits synovial fibroblasts proliferation and inflammatory cytokines secretion in rheumatoid arthritis through mediating p38MAPK signaling pathway.

Zhan-Chao Wang, Hua Lu, Qiang Zhou, Si-Ming Yu, Yu-Lun Mao, Hao-Jie Zhang, Ping-Chao Zhang, Wang-Jun Yan

Open access · greenAbstract read
In one paragraph

Article in International journal of clinical and experimental pathology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

30 citing papers in PubMed, 54 citations in OpenAlex.

  1. Review
  2. Article
  3. miR-144/451: A Regulatory Role in Inflammation.Current molecular medicine · 2025
    Review
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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

8 authors at 2 institutions in 1 country.

Zhan-Chao WangDepartment of Orthopedics, Xinhua Hospital (Chongming), Shanghai Jiaotong University Shanghai 202150, China.
Hua LuDepartment of Orthopedics, Xinhua Hospital, Shanghai Jiaotong University Shanghai 200092, China.
Qiang ZhouDepartment of Orthopedics, Xinhua Hospital (Chongming), Shanghai Jiaotong University Shanghai 202150, China.
Si-Ming YuDepartment of Orthopedics, Xinhua Hospital (Chongming), Shanghai Jiaotong University Shanghai 202150, China.
Yu-Lun MaoDepartment of Orthopedics, Xinhua Hospital (Chongming), Shanghai Jiaotong University Shanghai 202150, China.
Hao-Jie ZhangDepartment of Orthopedics, Xinhua Hospital (Chongming), Shanghai Jiaotong University Shanghai 202150, China.
Ping-Chao ZhangDepartment of Orthopedics, Xinhua Hospital (Chongming), Shanghai Jiaotong University Shanghai 202150, China.
Wang-Jun YanDepartment of Orthopedics, Changzheng Hospital, Second Military Medical University Shanghai 200061, China.
XinHua Hospital · CNSecond Military Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Rheumatoid arthritis is an autoimmune disease characterized as joint synovial inflammation. MicroRNA is a group of small noncoding RNA molecules discovered in recent years that can posttranscriptional regulate mRNA expression and involved in a variety processes of immune cell activation and differentiation. There is still lack of study about the role of miR-451 in rheumatoid arthritis. Synovial fibroblasts isolated from rheumatoid arthritis patients were cultured in vitro. Chemical synthesized miR-451 was lipo-transfected, real-time RT-PCR was applied to detect miR-451 expression level, and MTT method was used to detect the effect of miR-451 on synovial fibroblasts proliferation. Enzyme-linked immunosorbent assay was used to detect tumor necrosis factor TNF-α, IL-1β, and IL-6 level in the supernatant. Western blot was applied to test target protein p38 MAPK expression level. Our study found that synovial fibroblasts expressed higher miR-451 mRNA level in miR-451 treatment group. MiR-451 treatment significantly decreased cell proliferation ability (P < 0.05). Compared with the control, p38 MAPK protein expression reduced obviously in the miR-451 treatment group (P < 0.05). MiR-451 transfected synovial fibroblasts secreted lower levels of TNF-α (198 ± 12 pg/ml vs 124 ± 13 pg/ml, P < 0.01), IL-1β (352 ± 43 pg/ml vs 165 ± 87 pg/ml, P < 0.01), and IL-6 (487 ± 84 pg/ml vs 257 ± 92 pg/ml, P < 0.01). The results proved that miR-451 can down-regulate p38 MAPK protein expression, and reduce synovial fibroblasts proliferation and cytokine expression level.

Indexed as

Arthritis, RheumatoidBlotting, WesternCell ProliferationCells, CulturedCytokinesEnzyme-Linked Immunosorbent AssayFibroblastsGene Expression RegulationHumansInflammationMAP Kinase Signaling SystemMicroRNAsReal-Time Polymerase Chain ReactionSynovial MembraneTransfectionCytokinesMicroRNAsMIRN451 microRNA, humancell proliferationmiR-451rheumatoid arthritissynovial fibroblast

Identifiers

PMID26823778
PMCPMC4713564
OpenAlexW2411357740

What OpenQuestion holds

Textmetadata
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.