Evidence map›Paper›PMID 32908163›Full record

ArticleScientific reports2020

Deficiency of the SMOC2 matricellular protein impairs bone healing and produces age-dependent bone loss.

Supawich Morkmued, François Clauss, Brigitte Schuhbaur, Valérie Fraulob, Eric Mathieu, Joseph Hemmerlé, Hans Clevers, Bon-Kyoung Koo, Pascal Dollé, Agnès Bloch-Zupan and 1 more

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02397824 (Orodental Manifestations of Rare Diseases), which is not on this map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.6field-weighted citation impact, top 9% 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.

NCT02397824 recruitingnot on this map

Orodental Manifestations of Rare Diseases

TypeobservationalSponsorUniversity Hospital, Strasbourg, FranceRan2015 to 2035Enrolled1,300ConditionsRare Disease OrodontalArmsSalivary and blood samples
3 · Its place in the literature

Who cites it

15 citing papers in PubMed, 25 citations in OpenAlex.

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  14. Harnessing a Feasible and VersatileFrontiers in physiology · 2022
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  15. 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

11 authors at 6 institutions in 3 countries.

Supawich MorkmuedDevelopmental Biology and Stem Cells Department, Institute of Genetics and of Molecular and Cellular Biology (IGBMC), 1 rue Laurent Fries, BP 10142, 67404, Illkirch, France.
François ClaussFaculté de Chirurgie Dentaire, Université de Strasbourg, 8 rue Ste Elisabeth, 67000, Strasbourg, France.
Brigitte SchuhbaurDevelopmental Biology and Stem Cells Department, Institute of Genetics and of Molecular and Cellular Biology (IGBMC), 1 rue Laurent Fries, BP 10142, 67404, Illkirch, France.
Valérie FraulobDevelopmental Biology and Stem Cells Department, Institute of Genetics and of Molecular and Cellular Biology (IGBMC), 1 rue Laurent Fries, BP 10142, 67404, Illkirch, France.
Eric MathieuBiomaterials and Bioengineering, Université de Strasbourg, INSERM UMR1121, 11 rue Humann, 67000, Strasbourg, France.
Joseph HemmerléBiomaterials and Bioengineering, Université de Strasbourg, INSERM UMR1121, 11 rue Humann, 67000, Strasbourg, France.
Hans CleversHubrecht Institute, University Medical Center Utrecht, and University Utrecht, Utrecht, The Netherlands.
Bon-Kyoung KooHubrecht Institute, University Medical Center Utrecht, and University Utrecht, Utrecht, The Netherlands.
Pascal DolléDevelopmental Biology and Stem Cells Department, Institute of Genetics and of Molecular and Cellular Biology (IGBMC), 1 rue Laurent Fries, BP 10142, 67404, Illkirch, France.
Agnès Bloch-ZupanDevelopmental Biology and Stem Cells Department, Institute of Genetics and of Molecular and Cellular Biology (IGBMC), 1 rue Laurent Fries, BP 10142, 67404, Illkirch, France. agnes.bloch-zupan@unistra.fr.
Karen NiederreitherDevelopmental Biology and Stem Cells Department, Institute of Genetics and of Molecular and Cellular Biology (IGBMC), 1 rue Laurent Fries, BP 10142, 67404, Illkirch, France. karennied1@gmail.com.
Centre National de la Recherche Scientifique · FRUniversité de Strasbourg · FRHubrecht Institute for Developmental Biology and Stem Cell Research · NLInserm · FRInstitut de génétique et de biologie moléculaire et cellulaire · FRUniversity Medical Center Utrecht · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Secreted extracellular matrix components which regulate craniofacial development could be reactivated and play roles in adult wound healing. We report a patient with a loss-of-function of the secreted matricellular protein SMOC2 (SPARC related modular calcium binding 2) presenting severe oligodontia, microdontia, tooth root deficiencies, alveolar bone hypoplasia, and a range of skeletal malformations. Turning to a mouse model, Smoc2-GFP reporter expression indicates SMOC2 dynamically marks a range of dental and bone progenitors. While germline Smoc2 homozygous mutants are viable, tooth number anomalies, reduced tooth size, altered enamel prism patterning, and spontaneous age-induced periodontal bone and root loss are observed in this mouse model. Whole-genome RNA-sequencing analysis of embryonic day (E) 14.5 cap stage molars revealed reductions in early expressed enamel matrix components (Odontogenic ameloblast-associated protein) and dentin dysplasia targets (Dentin matrix acidic phosphoprotein 1). We tested if like other matricellular proteins SMOC2 was required for regenerative repair. We found that the Smoc2-GFP reporter was reactivated in adjacent periodontal tissues 4 days after tooth avulsion injury. Following maxillary tooth injury, Smoc2

Indexed as

AnimalsBone ResorptionCalcium-Binding ProteinsCyclooxygenase 2Gene Expression Regulation, DevelopmentalHumansMaleMatrix Metalloproteinase 9MiceMicroscopy, Electron, ScanningReal-Time Polymerase Chain ReactionRNA, MessengerToothCalcium-Binding ProteinsCyclooxygenase 2Matrix Metalloproteinase 9RNA, MessengerSMOC2 protein, human

Identifiers

PMID32908163
PMCPMC7481257
OpenAlexW3084111318

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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.