Evidence map›Paper›PMID 33008121›Full record

ArticleInternational journal of molecular sciences2020

Orthotopic Bone Formation by Streamlined Engineering and Devitalization of Human Hypertrophic Cartilage.

Sébastien Pigeot, Paul Emile Bourgine, Jaquiery Claude, Celeste Scotti, Adam Papadimitropoulos, Atanas Todorov, Christian Epple, Giuseppe M Peretti, Ivan Martin

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

11 citing papers in PubMed, 14 citations in OpenAlex.

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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

9 authors at 3 institutions in 2 countries.

Sébastien PigeotDepartment of Biomedicine, University Hospital Basel, University of Basel, 4031 Basel, Switzerland.
Paul Emile BourgineDepartment of Biomedicine, University Hospital Basel, University of Basel, 4031 Basel, Switzerland.ORCID 0000-0002-7639-6844
Jaquiery ClaudeDepartment of Surgery, University Hospital Basel, University of Basel, 4031 Basel, Switzerland.
Celeste ScottiNovartis Institutes for Biomedical Research, 4056 Basel, Switzerland.
Adam PapadimitropoulosDepartment of Biomedicine, University Hospital Basel, University of Basel, 4031 Basel, Switzerland.
Atanas TodorovDepartment of Biomedicine, University Hospital Basel, University of Basel, 4031 Basel, Switzerland.ORCID 0000-0002-1225-4302
Christian EppleDepartment of Surgery, University Hospital Basel, University of Basel, 4031 Basel, Switzerland.
Giuseppe M PerettiIRCCS Istituto Ortopedico Galeazzi, 20161 Milan, Italy.
Ivan MartinDepartment of Biomedicine, University Hospital Basel, University of Basel, 4031 Basel, Switzerland.ORCID 0000-0001-6493-0432
University of Basel · CHNovartis (Switzerland) · CHUniversity of Milan · IT

Funding

Eurostars Program E!7865Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung 310030-133110
6 · The paper itself

Abstract

Most bones of the human body form and heal through endochondral ossification, whereby hypertrophic cartilage (HyC) is formed and subsequently remodeled into bone. We previously demonstrated that HyC can be engineered from human mesenchymal stromal cells (hMSC), and subsequently devitalized by apoptosis induction. The resulting extracellular matrix (ECM) tissue retained osteoinductive properties, leading to ectopic bone formation. In this study, we aimed at engineering and devitalizing upscaled quantities of HyC ECM within a perfusion bioreactor, followed by in vivo assessment in an orthotopic bone repair model. We hypothesized that the devitalized HyC ECM would outperform a clinical product currently used for bone reconstructive surgery. Human MSC were genetically engineered with a gene cassette enabling apoptosis induction upon addition of an adjuvant. Engineered hMSC were seeded, differentiated, and devitalized within a perfusion bioreactor. The resulting HyC ECM was subsequently implanted in a 10-mm rabbit calvarial defect model, with processed human bone (Maxgraft

Indexed as

AnimalsApoptosisBone RemodelingBone SubstitutesCartilageCell DifferentiationExtracellular MatrixHumansMesenchymal Stem CellsMesenchymal Stem Cell TransplantationOsteogenesisRabbitsSkullTissue EngineeringTissue ScaffoldsWound HealingBone Substitutesapoptosisbioreactorsbone repairendochondral ossificationhypertrophic cartilageregenerative medicine

Identifiers

PMID33008121
PMCPMC7582540
OpenAlexW3089985264

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.