Evidence map›Paper›PMID 25545425›Full record

ArticleOsteoarthritis and cartilage2015

Transcriptional analysis of micro-dissected articular cartilage in post-traumatic murine osteoarthritis.

M D Gardiner, T L Vincent, C Driscoll, A Burleigh, G Bou-Gharios, J Saklatvala, H Nagase, A Chanalaris

Open access · hybridAbstract read
In one paragraph

Article in Osteoarthritis and cartilage, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed, 1 pooled it
3.8field-weighted citation impact, top 7% 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

49 citing papers in PubMed, 1 synthesis or guideline pooled it, 91 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. KLF transcription factors in bone diseases.Journal of cellular and molecular medicine · 2024
    Review
  11. Article
  12. Article
  13. Article
  14. Osteoarthritis: pathogenic signaling pathways and therapeutic targets.Signal transduction and targeted therapy · 2023
    Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  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

8 authors at 1 institution in 1 country.

M D GardinerKennedy Institute of Rheumatology, Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, University of Oxford, Old Road Campus, Roosevelt Drive, Headington, Oxford, OX3 7FY, UK. Electronic address: matthew.gardiner@kennedy.ox.ac.uk.
T L VincentKennedy Institute of Rheumatology, Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, University of Oxford, Old Road Campus, Roosevelt Drive, Headington, Oxford, OX3 7FY, UK. Electronic address: tonia.vincent@kennedy.ox.ac.uk.
C DriscollKennedy Institute of Rheumatology, Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, University of Oxford, Old Road Campus, Roosevelt Drive, Headington, Oxford, OX3 7FY, UK. Electronic address: clare.driscoll@kennedy.ox.ac.uk.
A BurleighKennedy Institute of Rheumatology, Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, University of Oxford, Old Road Campus, Roosevelt Drive, Headington, Oxford, OX3 7FY, UK. Electronic address: aburleigh@rvc.ac.uk.
G Bou-GhariosKennedy Institute of Rheumatology, Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, University of Oxford, Old Road Campus, Roosevelt Drive, Headington, Oxford, OX3 7FY, UK. Electronic address: g.bou-gharios@liverpool.ac.uk.
J SaklatvalaKennedy Institute of Rheumatology, Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, University of Oxford, Old Road Campus, Roosevelt Drive, Headington, Oxford, OX3 7FY, UK. Electronic address: jeremy.saklatvala@kennedy.ox.ac.uk.
H NagaseKennedy Institute of Rheumatology, Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, University of Oxford, Old Road Campus, Roosevelt Drive, Headington, Oxford, OX3 7FY, UK. Electronic address: hideaki.nagase@kennedy.ox.ac.uk.
A ChanalarisKennedy Institute of Rheumatology, Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, University of Oxford, Old Road Campus, Roosevelt Drive, Headington, Oxford, OX3 7FY, UK. Electronic address: anastasios.chanalaris@kennedy.ox.ac.uk.
Nuffield Orthopaedic Centre · GB

Funding

TIMP Engineering and Application to ArthritisR01AR040994 · NIAMS · UNIVERSITY OF KANSAS MEDICAL CENTER · PI BREW, KEITH · 1991 to 2013
$4.8M
Arthritis Research UKMedical Research Council MR/K006312/1NIAMS NIH HHS AR40994Wellcome Trust 088844/Z/09/Z
6 · The paper itself

Abstract

objectiveIdentify gene changes in articular cartilage of the medial tibial plateau (MTP) at 2, 4 and 8 weeks after destabilisation of the medial meniscus (DMM) in mice. Compare our data with previously published datasets to ascertain dysregulated pathways and genes in osteoarthritis (OA).

designRNA was extracted from the ipsilateral and contralateral MTP cartilage, amplified, labelled and hybridized on Illumina WGv2 microarrays. Results were confirmed by real-time polymerase chain reaction (PCR) for selected genes.

resultsTranscriptional analysis and network reconstruction revealed changes in extracellular matrix and cytoskeletal genes induced by DMM. TGFβ signalling pathway and complement and coagulation cascade genes were regulated at 2 weeks. Fibronectin (Fn1) is a hub in a reconstructed network at 2 weeks. Regulated genes decrease over time. By 8 weeks fibromodulin (Fmod) and tenascin N (Tnn) are the only dysregulated genes present in the DMM operated knees. Comparison with human and rodent published gene sets identified genes overlapping between our array and eight other studies.

conclusionsCartilage contributes a minute percentage to the RNA extracted from the whole joint (<0.2%), yet is sensitive to changes in gene expression post-DMM. The post-DMM transcriptional reprogramming wanes over time dissipating by 8 weeks. Common pathways between published gene sets include focal adhesion, regulation of actin cytoskeleton and TGFβ. Common genes include Jagged 1 (Jag1), Tetraspanin 2 (Tspan2), neuroblastoma, suppression of tumourigenicity 1 (Nbl1) and N-myc downstream regulated gene 2 (Ndrg2). The concomitant genes and pathways we identify may warrant further investigation as biomarkers or modulators of OA.

Indexed as

Adaptor Proteins, Signal TransducingAnimalsCalcium-Binding ProteinsCartilage, ArticularCell Cycle ProteinsDisease Models, AnimalExtracellular Matrix ProteinsFibromodulinFibronectinsIntercellular Signaling Peptides and ProteinsJagged-1 ProteinMaleMembrane ProteinsMenisci, TibialMiceMice, Inbred C57BLAdaptor Proteins, Signal TransducingCalcium-Binding ProteinsCell Cycle ProteinsExtracellular Matrix ProteinsFibromodulinFibronectinsFMOD protein, humanFmod protein, mouseIntercellular Signaling Peptides and ProteinsJAG1 protein, humanJag1 protein, mouseJagged-1 ProteinMembrane ProteinsNbl1 protein, mouseNdr2 protein, mouseNerve Tissue ProteinsProteinsProteoglycansSerrate-Jagged ProteinsTenascintenascin-N protein, mouseTetraspaninsTransforming Growth Factor betaTspan2 protein, mouseDestabilisation of the medial meniscus (DMM)FibromodulinFibronectinMicroarrayOsteoarthritisTenascin

Identifiers

PMID25545425
PMCPMC4373757
OpenAlexW2038237044

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.