Evidence map›Paper›PMID 30283907›Full record

ArticleJBMR plus2018

Molecular Phenotyping of Telomerized Human Bone Marrow Skeletal Stem Cells Reveals a Genetic Program of Enhanced Proliferation and Maintenance of Differentiation Responses.

Natalie A Twine, Linda Harkness, James Adjaye, Abdullah Aldahmash, Marc R Wilkins, Moustapha Kassem

Open access · goldAbstract read
In one paragraph

Article in JBMR plus, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

17 citing papers in PubMed, 26 citations in OpenAlex.

  1. Generation ofJBMR plus · 2026
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  6. Identifying Biomarkers for Osteogenic Potency Assay Development.Advances in experimental medicine and biology · 2023
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  8. Bioelectronic cell-based device provides a strategy for the treatment of the experimental model of multiple sclerosis.Journal of controlled release : official journal of the Controlled Release Society · 2022
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  11. Article
  12. Review
  13. Correlation ofCell journal · 2021
    Article
  14. Article
  15. Review
  16. Review
  17. 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

6 authors at 5 institutions in 4 countries.

Natalie A TwineSystems Biology Initiative School of Biotechnology and Biomolecular Sciences University of New South Wales Sydney Australia.
Linda HarknessDepartment of Endocrinology and Metabolism Endocrine Research Laboratory (KMEB) Odense University Hospital Odense Denmark.
James AdjayeInstitute for Stem Cell Research and Regenerative Medicine Faculty of Medicine Heinrich Heine University Düsseldorf Germany.
Abdullah AldahmashStem Cell Unit Department of Anatomy, Faculty of Medicine King Saud University Riyadh Saudi Arabia.
Marc R WilkinsSystems Biology Initiative School of Biotechnology and Biomolecular Sciences University of New South Wales Sydney Australia.
Moustapha KassemSystems Biology Initiative School of Biotechnology and Biomolecular Sciences University of New South Wales Sydney Australia.
Odense University Hospital · DKCommonwealth Scientific and Industrial Research Organisation · AUHeinrich Heine University Düsseldorf · DEKing Saud University · SAUNSW Sydney · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Long-term in vitro expansion of bone marrow stromal (skeletal) stem cells (also known as human mesenchymal stem cells [hMSC]) is associated with replicative senescence and impaired functions. We have previously reported that telomerization of hMSC through hTERT overexpression led to bypassing a replicative senescence phenotype and improved in vitro and in vivo functions. However, the molecular consequence of telomerization is poorly characterized. Thus, we compared the molecular phenotype of a well-studied telomerized hMSC (hMSC-TERT) cell line with primary hMSC. At a cellular level, both cell populations exhibited strong concordance for the known hMSC CD markers, similar responses to osteoblast (OB) differentiation induction, and formed heterotopic bone in vivo. Overall gene expression was highly correlated between both cell types with an average Pearson's correlation coefficient (R

Indexed as

BONE MARROW STROMAL (SKELETAL) STEM CELLS (hMSC)HMSC‐TERTMOLECULAR PHENOTYPEOSTEOBLASTSTELOMERIZATION

Identifiers

PMID30283907
PMCPMC6139702
OpenAlexW2794535189

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.