Evidence map›Paper›PMID 30361290›Full record

ArticleBioscience reports2018

Long non-coding RNA DANCR regulates proliferation and apoptosis of chondrocytes in osteoarthritis via miR-216a-5p-JAK2-STAT3 axis.

Lei Zhang, Pin Zhang, Xiangyi Sun, Liwu Zhou, Jianning Zhao

Open access · goldAbstract read
In one paragraph

Article in Bioscience reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed, 1 pooled it
2.8field-weighted citation impact, top 9% 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, 1 synthesis or guideline pooled it, 58 citations in OpenAlex.

  1. Pooled it
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  7. Article
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  14. Review
  15. Roles of long non‑coding RNA in osteoarthritis (Review).International journal of molecular medicine · 2021
    Review
  16. Role of long non-coding RNAs in adipogenesis: State of the art and implications in obesity and obesity-associated diseases.Obesity reviews : an official journal of the International Association for the Study of Obesity · 2021
    Review
  17. Article
  18. Article
  19. Crosstalk Among circRNA/lncRNA, miRNA, and mRNA in Osteoarthritis.Frontiers in cell and developmental biology · 2021
    Review
  20. 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

5 authors at 2 institutions in 1 country.

Lei ZhangDepartment of Orthopedics, Jinling Hospital, Nanjing University, School of Medicine, Nanjing 210002, China.
Pin ZhangDepartment of Orthopedics, Jinling Clinical Medical College of Nanjing Medical University, Nanjing 210002, China.
Xiangyi SunDepartment of Orthopedics, Jinling Clinical Medical College of Nanjing Medical University, Nanjing 210002, China.
Liwu ZhouDepartment of Orthopedics, Jinling Hospital, Nanjing University, School of Medicine, Nanjing 210002, China.
Jianning ZhaoDepartment of Orthopedics, Jinling Hospital, Nanjing University, School of Medicine, Nanjing 210002, China zhaojianningmyc@163.com.ORCID 0000-0003-4645-0552
Nanjing General Hospital of Nanjing Military Command · CNNanjing Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Osteoarthritis (OA) is one of the most common chronic joint disease. Long non-coding RNAs (lncRNAs) have been confirmed to play important roles in a variety of diseases including OA. However, the underlying mechanism of lncRNA differentiation antagonizing non-protein coding RNA (DANCR) in OA has not been well elucidated. The expression of DANCR in cartilage tissues from OA patients was detected using quantitative real-time PCR. After cell transfection, the effects of DANCR inhibition on the proliferation, apoptosis and inflammatory factors of OA chondrocytes were detected using Cell Counting Kit-8 assay and flow cytometry assay. Novel target of DANCR was then identified through bioinformatics analysis and confirmed by luciferase reporter assay and RNA immunoprecipitation assay. The expression of DANCR was significantly increased in OA patients. Function assays demonstrated that DANCR suppression inhibited the proliferation, inflammation, and promoted apoptosis of chondrocytes cells. Additionally, DANCR regulated survival of OA chondrocytes through acting as a competitive endogenous RNA for miR-216a-5p. Furthermore, JAK2 was a direct target of miR-216a-5p, and DANCR regulated the JAK2/STAT3 signal pathway through miR-216a-5p in OA chondrocytes. In the present study, we concluded that DANCR promoted the proliferation, inflammation, and reduced cell apoptosis in OA chondrocytes through regulating miR-216a-5p/JAK2/STAT3 signaling pathway, indicating DANCR might be a useful biomarker and potential therapeutic target for OA treatment.

Indexed as

Gene Expression RegulationApoptosisCell ProliferationCells, CulturedChondrocytesHumansJanus Kinase 2MicroRNAsOsteoarthritisRNA, Long NoncodingSignal TransductionSTAT3 Transcription FactorDANCR long noncoding RNA, humanJAK2 protein, humanJanus Kinase 2MicroRNAsMIRN216 microRNA, humanRNA, Long NoncodingSTAT3 Transcription FactorDANCRJAK2miR-216a-5pOsteoarthritisSTAT3

Identifiers

PMID30361290
PMCPMC6294632
OpenAlexW2898437135

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Registered trials

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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.