Evidence map›Paper›PMID 26796346›Full record

ReviewMatrix biology : journal of the International Society for Matrix Biology

Syndecan-4 in intervertebral disc and cartilage: Saint or synner?

Abbie L A Binch, Irving M Shapiro, Makarand V Risbud

Open access · greenAbstract readReview
In one paragraph

Review in Matrix biology : journal of the International Society for Matrix Biology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
3.9field-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

30 citing papers in PubMed, 40 citations in OpenAlex.

  1. Review
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  15. Article
  16. Complexity of matrix phenotypes.Matrix biology plus · 2020
    Article
  17. Article
  18. p16Matrix biology : journal of the International Society for Matrix Biology · 2019
    Article
  19. Article
  20. Molecular Mechanisms of Intervertebral Disc Degeneration.Spine surgery and related research · 2019
    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

3 authors at 1 institution in 1 country.

Abbie L A BinchDepartment of Orthopaedic Surgery, Sidney Kimmel Medical College and Graduate Program in Cell and Developmental Biology, Thomas Jefferson University, Philadelphia, USA. Electronic address: Abbie.Binch@Jefferson.edu.
Irving M ShapiroDepartment of Orthopaedic Surgery, Sidney Kimmel Medical College and Graduate Program in Cell and Developmental Biology, Thomas Jefferson University, Philadelphia, USA. Electronic address: Irving.Shapiro@Jefferson.edu.
Makarand V RisbudDepartment of Orthopaedic Surgery, Sidney Kimmel Medical College and Graduate Program in Cell and Developmental Biology, Thomas Jefferson University, Philadelphia, USA. Electronic address: Makarand.Risbud@Jefferson.edu.
Thomas Jefferson University · US

Funding

Role of HIF-1 in Intervertebral Disc FunctionR01AR055655 · NIAMS · THOMAS JEFFERSON UNIVERSITY · PI RISBUD, MAKARAND V · 2008 to 2023
$6.1M
Regeneration of Nucleus Pulposus by Tissue EngineeringR01AR050087 · NIAMS · THOMAS JEFFERSON UNIVERSITY · PI RISBUD, MAKARAND V, SHAPIRO, IRVING M · 2005 to 2013
$3.0M
Disruption of Osmoregulation Promotes Degenerative Disc DiseaseR01AR064733 · NIAMS · THOMAS JEFFERSON UNIVERSITY · PI RISBUD, MAKARAND V, SHAPIRO, IRVING M · 2014 to 2018
$2.4M
NIAMS NIH HHS R01 AR050087NIAMS NIH HHS R01 AR055655NIAMS NIH HHS R01 AR064733
6 · The paper itself

Abstract

The ECM of the intervertebral disc and articular cartilage contains a highly organised network of collagens and proteoglycans which resist compressive forces applied to these tissues. A pathological hallmark of the intervertebral disc is the imbalance between production of anabolic and catabolic factors by the resident cells. This process is thought to be mediated by pro-inflammatory cytokines, predominantly TNF-α and IL-1β, which upregulate expression of matrix degrading enzymes such as MMPs and ADAMTSs. This imbalance ultimately results in tissue degeneration causing failure of the biomechanical function of the tissues. A similar cascade of events is thought to occur in articular cartilage during development of osteoarthritis. Within these skeletal tissues a small, cell surface heparan sulphate proteoglycan; syndecan-4 (SDC4) has been implicated in maintaining physiological functions. However in the degenerating niche of the intervertebral disc and cartilage, dysregulated activities of this molecule may exacerbate pathological changes. Studies in recent years have elucidated a role for SDC4 in mediating matrix degradation in both intervertebral discs and cartilage by controlling ADAMTS-5 function and MMP3 expression. Discourse presented in this review highlights the potential of SDC4 as a possible therapeutic target in slowing the progression of ECM degradation in both degenerative disc disease and osteoarthritis.

Indexed as

ADAMTS5 ProteinCartilageExtracellular MatrixGene Expression RegulationHumansInterleukin-1betaIntervertebral DiscJoint DiseasesMatrix Metalloproteinase 3Syndecan-4Tumor Necrosis Factor-alphaADAMTS5 ProteinADAMTS5 protein, humanIL1B protein, humanInterleukin-1betaMatrix Metalloproteinase 3MMP3 protein, humanSDC4 protein, humanSyndecan-4TNF protein, humanTumor Necrosis Factor-alphaCartilageCytokinesDisc degenerationExtracellular matrixIntervertebral discSyndecan-4

Identifiers

PMID26796346
PMCPMC4875798
OpenAlexW2267308669

What OpenQuestion holds

Textmetadata
LicenceTDM
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.