Evidence map›Paper›PMID 24482033›Full record

ArticleJournal of dental research2014

Recombinant biglycan promotes bone morphogenetic protein-induced osteogenesis.

P A Miguez, M Terajima, H Nagaoka, J A R Ferreira, K Braswell, C C Ko, M Yamauchi

Abstract read
In one paragraph

Article in Journal of dental research, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.6field-weighted citation impact, top 32% 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

10 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. Biglycan promotes tumour proliferation and invasion in human colon cancers.The Journal of international medical research · 2024
    Article
  3. Review
  4. Article
  5. Stability and remineralization of proteoglycan-infused dentin substrate.Dental materials : official publication of the Academy of Dental Materials · 2021
    Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Soluble biglycan as a biomarker of inflammatory renal diseases.The international journal of biochemistry & cell biology · 2014
    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

7 authors at 1 institution in 1 country.

P A MiguezNorth Carolina Oral Health Institute, The University of North Carolina at Chapel Hill, USA.
M Terajima
H Nagaoka
J A R Ferreira
K Braswell
C C Ko
M Yamauchi
University of North Carolina at Chapel Hill · US

Funding

Matrix-assisted Craniofacial Bone RegenerationR21DE020909 · NIDCR · UNIV OF NORTH CAROLINA CHAPEL HILL · PI YAMAUCHI, MITSUO · 2011 to 2012
$406k
Collagen Glycosylation, Maturation and MineralizationR21AR060978 · NIAMS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI YAMAUCHI, MITSUO · 2012 to 2013
$352k
NIAMS NIH HHS AR060978NIAMS NIH HHS R21 AR060978NIDCR NIH HHS R21 DE020909
6 · The paper itself

Abstract

The aim of this study was to determine the effects of glutathione-S-transferase-fused recombinant biglycan (GST-BGN) on craniofacial bone regeneration. We recently demonstrated a positive effect of tissue-derived BGN on bone morphogenetic protein 2 (BMP-2) function, which is exerted likely via the BGN core protein. Here, we investigated the effects of GST-BGN lacking any posttranslational modifications on BMP-2 function in vitro and in vivo. In the C2C12 cell culture system, BMP-2-induced Smad 1/5/8 phosphorylation and alkaline phosphatase activity were both enhanced by the addition of GST-BGN. For the in vivo effect, we employed a Sprague-Dawley rat mandible defect model utilizing 1 µg (optimal) or 0.1 µg (suboptimal) of BMP-2 combined with 0, 2, 4, or 8 µg of GST-BGN. At 2 weeks post-surgery, newly formed bone was evaluated by microcomputed tomography and histologic analyses. The results revealed that the greatest amounts of bone within the defect were formed in the groups of suboptimal BMP-2 combined with 4 or 8 µg of GST-BGN. Also, bone was well organized versus that formed by the optimal dose of BMP. These results indicate that recombinant BGN is an efficient substrate to promote low-dose BMP-induced osteogenesis.

Indexed as

Acid PhosphataseAlkaline PhosphataseAnimalsBiglycanBiomarkersBone DensityBone Morphogenetic Protein 2Bone RegenerationCell Culture TechniquesCell LineCollagenGlutathione TransferaseIsoenzymesMandibular DiseasesMAP Kinase Signaling SystemOsteogenesisAcid PhosphataseAlkaline PhosphataseBgn protein, ratBiglycanBiomarkersBmp2 protein, ratBone Morphogenetic Protein 2CollagenGlutathione TransferaseIsoenzymesRecombinant ProteinsSmad1 ProteinSmad1 protein, ratSmad5 ProteinSmad5 protein, ratSmad8 ProteinSmad9 protein, ratTartrate-Resistant Acid Phosphatasebone regenerationcritical-sized defectgrowth factormicrocomputed tomographyproteoglycanSmad 1/5/8

Identifiers

PMID24482033
PMCPMC3957343
OpenAlexW2114099139

What OpenQuestion holds

Textmetadata
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.