Evidence map›Paper›PMID 27832770›Full record

ArticleBMC musculoskeletal disorders2016

The tenocyte phenotype of human primary tendon cells in vitro is reduced by glucocorticoids.

Christoph Spang, Jialin Chen, Ludvig J Backman

Open access · goldAbstract read
In one paragraph

Article in BMC musculoskeletal disorders, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.9field-weighted citation impact, top 15% 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

16 citing papers in PubMed, 31 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Prolyl-Hydroxyproline Promotes Structural Matrix Organization in 3D Equine Tendon Proper and Peritenon Post-Injury Model.Journal of orthopaedic research : official publication of the Orthopaedic Research Society · 2026
    Article
  4. Review
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  13. Sustained Exposure of Substance P Causes Tendinopathy.International journal of molecular sciences · 2020
    Article
  14. Effects and Mechanism of Berberine on the Dexamethasone-Induced Injury of Human Tendon Cells.Evidence-based complementary and alternative medicine : eCAM · 2020
    Article
  15. Article
  16. Article
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

3 authors at 2 institutions in 2 countries.

Christoph SpangDepartment of Integrative Medical Biology, Anatomy, Umeå University, SE-901 87, Umeå, Sweden. christoph.spang@umu.se.ORCID 0000-0002-9977-334X
Jialin ChenDepartment of Integrative Medical Biology, Anatomy, Umeå University, SE-901 87, Umeå, Sweden.
Ludvig J BackmanDepartment of Integrative Medical Biology, Anatomy, Umeå University, SE-901 87, Umeå, Sweden.
Umeå University · SEChristophorus Kliniken · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe use of corticosteroids (e.g., dexamethasone) as treatment for tendinopathy has recently been questioned as higher risks for ruptures have been observed clinically. In vitro studies have reported that dexamethasone exposed tendon cells, tenocytes, show reduced cell viability and collagen production. Little is known about the effect of dexamethasone on the characteristics of tenocytes. Furthermore, there are uncertainties about the existence of apoptosis and if the reduction of collagen affects all collagen subtypes.

methodsWe evaluated these aspects by exposing primary tendon cells to dexamethasone (Dex) in concentrations ranging from 1 to 1000 nM. Gene expression of the specific tenocyte markers scleraxis (Scx) and tenomodulin (Tnmd) and markers for other mesenchymal lineages, such as bone (Alpl, Ocn), cartilage (Acan, Sox9) and fat (Cebpα, Pparg) was measured via qPCR. Cell viability and proliferation was calculated using a MTS Assay. Cell death was measured by LDH assay and cleaved caspase-3 using Western Blot. Gene expression of collagen subtypes Col1, Col3 and Col14 was analyzed using qPCR.

resultsStimulation with Dex decreased cell viability and LDH levels. Dex also induced a significant reduction of Scx gene expression and a marked loss of fibroblast like cell shape. The mRNA for all examined collagen subtypes was found to be down-regulated. Among non-tendinous genes only Pparg was significantly increased, whereas Acan, Alpl and Sox9 were reduced.

conclusionsThese results indicate a Dex induced phenotype drift of the tenocytes by reducing scleraxis expression. Reduction of several collagen subtypes, but not cell death, seems to be a feature of Dex induced tissue degeneration.

Indexed as

Basic Helix-Loop-Helix ProteinsCell DeathCollagenDexamethasoneFemaleGlucocorticoidsHumansMaleMembrane ProteinsMiddle AgedPhenotypePrimary Cell CultureTendinopathyTenocytesBasic Helix-Loop-Helix ProteinsCollagenDexamethasoneGlucocorticoidsMembrane ProteinsSCX protein, humanTNMD protein, humanCell viabilityCollagenDexamethasonePhenotypeScleraxisTendinopathyTendon cellsTenocytes

Identifiers

PMID27832770
PMCPMC5105245
OpenAlexW2552432712

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.