Evidence map›Paper›PMID 26735178›Full record

ArticleOncotarget2016

Nucleus pulposus phenotypic markers to determine stem cell differentiation: fact or fiction?

Abbey A Thorpe, Abbie L A Binch, Laura B Creemers, Christopher Sammon, Christine L Le Maitre

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
4.4field-weighted citation impact, top 5% 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

35 citing papers in PubMed, 64 citations in OpenAlex.

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  11. Frontiers in molecular biosciences · 2022
    Article
  12. Stem cells in intervertebral disc regeneration-more talk than action?Biocell : official journal of the Sociedades Latinoamericanas de Microscopia Electronica ... et. al · 2021
    Article
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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 2 countries.

Abbey A ThorpeBiomolecular Sciences Research Centre, Sheffield Hallam University, Sheffield, UK.
Abbie L A BinchBiomolecular Sciences Research Centre, Sheffield Hallam University, Sheffield, UK.
Laura B CreemersUMC Utrecht, Orthopaedics Department, Utrecht, Netherlands.
Christopher SammonMaterials and Engineering Research Institute, Sheffield Hallam University, Sheffield, UK.
Christine L Le MaitreBiomolecular Sciences Research Centre, Sheffield Hallam University, Sheffield, UK.
Sheffield Hallam University · GBUniversity Medical Center Utrecht · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Progress in mesenchymal stem cell (MSC) based therapies for nucleus pulposus (NP) regeneration are hampered by a lack of understanding and consensus of the normal NP cell phenotype. Despite the recent consensus paper on NP markers, there is still a need to further validate proposed markers. This study aimed to determine whether an NP phenotypic profile could be identified within a large population of mature NP samples.qRT-PCR was conducted to assess mRNA expression of 13 genes within human non-degenerate articular chondrocytes (AC) (n=10) and NP cells extracted from patients across a spectrum of histological degeneration grades (n=71). qRT-PCR results were used to select NP marker candidates for protein expression analysis.Differential expression at mRNA between AC and non-degenerate NP cells was only observed for Paired Box Protein 1 (PAX1) and Forkhead box F1 (FOXF1). In contrast no other previously suggested markers displayed differential expression between non-degenerate NP and AC at mRNA level. PAX1 and FOXF1 protein expression was significantly higher in the NP compared to annulus fibrosus (AF), cartilaginous endplate (CEP) and AC. In contrast Laminin-5 (LAM-332), Keratin-19 (KRT-19) and Hypoxia Inducible Factor 1 alpha (HIF1α) showed no differential expression in NP cells compared with AC cells.A marker which exclusively differentiates NP cells from AF and AC cells remains to be identified, raising the question: is the NP a heterogeneous population of cells? Or does the natural biological variation during IVD development, degeneration state and even the life cycle of cells make finding one definitive marker impossible?

Indexed as

Cartilage, ArticularCell Adhesion MoleculesCell DifferentiationChondrocytesForkhead Transcription FactorsGenetic MarkersGuided Tissue RegenerationHumansHypoxia-Inducible Factor 1, alpha SubunitIntervertebral DiscIntervertebral Disc DegenerationKalininKeratin-19Mesenchymal Stem CellsMesenchymal Stem Cell TransplantationPaired Box Transcription FactorsCell Adhesion MoleculesForkhead Transcription FactorsFOXF1 protein, humanGenetic MarkersHIF1A protein, humanHypoxia-Inducible Factor 1, alpha SubunitKalininKeratin-19Paired Box Transcription FactorsPAX1 transcription factorRNA, MessengerFOXF1nucleus pulposusPathology Sectionphenotypic markersregenerationstem cells PAX1

Identifiers

PMID26735178
PMCPMC4823028
OpenAlexW2214723042

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.