Evidence map›Paper›PMID 32083281›Full record

ArticleBioscience reports2020

Down-regulation of microRNA-203a suppresses IL-1β-induced inflammation and cartilage degradation in human chondrocytes through Smad3 signaling.

Yongbo An, Guang Wan, Jingang Tao, Mingxing Cui, Qinglan Zhou, Wengen Hou

Open access · goldAbstract read
In one paragraph

Article in Bioscience reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
1.9field-weighted citation impact, top 14% 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

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

  1. Pooled it
  2. Review
  3. Article
  4. Review
  5. Review
  6. Multi-omics molecular biomarkers and database of osteoarthritis.Database : the journal of biological databases and curation · 2022
    Article
  7. Review
  8. Article
  9. microRNA-130b downregulation potentiates chondrogenic differentiation of bone marrow mesenchymal stem cells by targeting SOX9.Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas · 2021
    Article
  10. Crosstalk Among circRNA/lncRNA, miRNA, and mRNA in Osteoarthritis.Frontiers in cell and developmental biology · 2021
    Review
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 1 institution in 1 country.

Yongbo AnDepartment of Orthopedics II, The First Affiliated Hospital of Xinxiang Medical University, Weihui 453100, Henan, China.
Guang WanDepartment of Orthopedics IV, The First Affiliated Hospital of Xinxiang Medical University, Weihui 453100, Henan, China.
Jingang TaoDepartment of Orthopedics I, The First Affiliated Hospital of Xinxiang Medical University, Weihui 453100, Henan, China.
Mingxing CuiDepartment of Orthopedics II, The First Affiliated Hospital of Xinxiang Medical University, Weihui 453100, Henan, China.
Qinglan ZhouDepartment of Orthopedics I, The First Affiliated Hospital of Xinxiang Medical University, Weihui 453100, Henan, China.
Wengen HouDepartment of Orthopedics II, The First Affiliated Hospital of Xinxiang Medical University, Weihui 453100, Henan, China.
First Affiliated Hospital of Xinxiang Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Osteoarthritis (OA) is a chronic and prevalent degenerative musculoskeletal disorder, which is characterized by articular cartilage degradation and joint inflammation. MicroRNA-203a (miR-203a) has been shown to be involved in multiple pathological processes during OA, but little is known about its function in chondrocyte extracellular matrix (ECM) degradation. In the present study, we aimed to elucidate the effects of miR-203a on articular cartilage degradation and joint inflammation. We observed that the miR-203a level was significantly up-regulated in OA tissues and in an in vitro model of OA, respectively. Inhibition of miR-203a significantly alleviated the interleukin (IL)-1β-induced inflammatory response and ECM degradation in chondrocytes. Moreover, mothers against decapentaplegic homolog 3 (Smad3), a key factor in maintaining chondrocyte homeostasis, was identified as a putative target of miR-203a in chondrocytes. More importantly, inhibition of Smad3 impaired the inhibitory effects of the miR-203a on IL-1β-induced inflammatory response and ECM degradation. Collectively, these results demonstrated that miR-203a may contribute to articular cartilage degradation of OA by targeting Smad3, suggesting a novel therapeutic target for the treatment of OA.

Indexed as

CartilageCartilage, ArticularCells, CulturedChinaChondrocytesFemaleHumansInflammationInterleukin-1betaMaleMicroRNAsOsteoarthritisSignal TransductionSmad3 ProteinIL1B protein, humanInterleukin-1betaMicroRNAsMIRN203 microRNA, humanSmad3 ProteinSMAD3 protein, humanarticular cartilageECMinflammatory cytokinesmiR-203aOsteoarthritis

Identifiers

PMID32083281
PMCPMC7070148
OpenAlexW3007880665

What OpenQuestion holds

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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.