Evidence map›Paper›PMID 26244598›Full record

ArticleScientific reports2015

MiR-210 inhibits NF-κB signaling pathway by targeting DR6 in osteoarthritis.

Dawei Zhang, Xiaorui Cao, Jun Li, Guangyue Zhao

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 67 papers.

0numbers the graph read from it
0cells of the map it votes in
67citing papers in PubMed
4.6field-weighted citation impact, top 4% 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

67 citing papers in PubMed, 111 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. The Role of MicroRNAs in the Pathophysiology of Osteoarthritis.International journal of molecular sciences · 2024
    Review
  6. Article
  7. Article
  8. Review
  9. SilencingBiomolecules · 2023
    Article
  10. Article
  11. Article
  12. The Role of microRNAs in Inflammation.International journal of molecular sciences · 2022
    Review
  13. Article
  14. Article
  15. Review
  16. Article
  17. Review
  18. Article
  19. Review
  20. Article

7 more citing papers are in PubMed but not listed here.

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

4 authors at 2 institutions in 1 country.

Dawei ZhangDepartment of Orthopedics, Xijing Hospital, Fourth Military Medical University, Xi'an 710032, China.
Xiaorui CaoDepartment of Orthopedics, Xijing Hospital, Fourth Military Medical University, Xi'an 710032, China.
Jun LiDepartment of Orthopedics, Xijing Hospital, Fourth Military Medical University, Xi'an 710032, China.
Guangyue ZhaoDepartment of Orthopedics, Xijing Hospital, Fourth Military Medical University, Xi'an 710032, China.
Air Force Medical University · CNXijing Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Osteoarthritis (OA) is characterized by degradation of articular cartilage and joint inflammation. MicroRNAs have been proved to play an important role in the regulation of chondrogenesis. Previous study showed that microRNA-210 (miR-210) was probably associated with osteoarthritis, while the function of miR-210 in osteoarthritis still remains unknown. The aim of the present study was to investigate the protective effect of miR-210 on osteoarthritis. In the in vitro study, miR-210 level in chondrocytes was decreased after treatment with lipopolysaccharide (LPS). Transfection with miR-210 mimic inhibited LPS-induced pro-inflammatory cytokines production, cell viability reduction and cell apoptosis. Results of luciferase activity assay showed that miR-210 targeted 3'-UTR of death receptor 6 (DR6) to inhibit its expression. MiR-210 mimic and DR6 siRNA transfection inhibited the activation of NF-κB pathway and cell apoptosis of chondrocytes. For the in vivo study, OA model was established on rats by anterior cruciate ligament transection (ACLT). MiR-210 expression is reduced in OA rats. MiR-210 over-expressing lentivirus was injected into the OA rats. Cytokines production, and NF-κB and DR6 expression in OA rats was inhibited by miR-210 overexpression. The results demonstrated that miR-210 decreased inflammation in articular cavity in OA rats by targeting DR6 and inhibiting NF-κB signaling pathway.

Indexed as

Signal Transduction3' Untranslated RegionsAnimalsCytokinesDisease Models, AnimalFemaleGene Expression RegulationLipopolysaccharidesMicroRNAsNF-kappa BOsteoarthritisRatsRats, Sprague-DawleyReceptors, Tumor Necrosis Factor3' Untranslated RegionsCytokinesLipopolysaccharidesMicroRNAsMIRN210 microRNA, ratNF-kappa BReceptors, Tumor Necrosis Factor

Identifiers

PMID26244598
PMCPMC4525484
OpenAlexW1059897138

What OpenQuestion holds

Textmetadata
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.