Evidence map›Paper›PMID 25480698›Full record

ArticleChild's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery2015

Proposing the use of dental pulp stem cells as a suitable biological model of neurofibromatosis type 1.

Paula Nascimento Almeida, Gustavo Torres Souza, Camila Maurmann de Souza, Rafaella Souza Salomão de Zanette, Claudinéia Pereira Maranduba, João Vitor Paes Rettore, Marcelo Oliveira de Santos, Antônio Márcio Resende do Carmo, Carlos Magno Costa da Maranduba, Fernando Sá de Silva

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Article in Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact, top 90% 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

4 citing papers in PubMed, 7 citations in OpenAlex.

  1. Effects of resveratrol on the proliferation and osteogenic differentiation of deciduous dental pulp stem cells from neurofibromatosis type 1 patient.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2021
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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

10 authors at 1 institution in 1 country.

Paula Nascimento AlmeidaLaboratory of Human Genetics and Cell Therapy, Biology Department, Biological Sciences Institute, Federal University of Juiz de Fora, Juiz de Fora, 36036-900, Brazil.
Gustavo Torres Souza
Camila Maurmann de Souza
Rafaella Souza Salomão de Zanette
Claudinéia Pereira Maranduba
João Vitor Paes Rettore
Marcelo Oliveira de Santos
Antônio Márcio Resende do Carmo
Carlos Magno Costa da Maranduba
Fernando Sá de Silva
Universidade Federal de Juiz de Fora · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThis study aims to propose the dental pulp stem cells (DPSCs) as a model for studying two features related to neurofibromatosis type 1 (NF1), i.e. augmented proliferative capacity and altered osteogenic differentiation.

methodsWe isolated a DPSC from the pulp of deciduous teeth of a 6-year-old NF1 patient and two other healthy children of similar age. Cell proliferation was assayed by counting with a haemocytometer after successive cell re-plating. In order to compare osteogenic differentiation, we used osteoblast-differentiating medium and quantified alizarin stain, which relates to degree of calcification, and evaluated the expression of osteoblastic markers by reverse transcription polymerase chain reaction (RT-PCR).

resultsThe DPSCs isolated from the NF1 patient displayed a greater rate of proliferation when compared to the control cells. Osteogenic differentiation occurred as expected for both NF1 and control, which concerned cell morphology and expression of osteoblast marker genes ALP, BMP2, BMP4, OCN and SPP1. However, alizarin staining denoted a markedly lower calcification level in the cells from the NF1-diagnosed child, considering that less calcium deposits were visualized under light microscopy and a smaller amount of alizarin could be quantified by spectrophotometry after extraction from the stained cells.

conclusionDPSCs seem to be useful as a model for studying NF1 and predicting prognosis of patients, since their in vitro behaviour seems to mimic at least two features of this disorder: higher tendency to develop bone abnormalities and neoplastic cell proliferation.

Indexed as

Alkaline PhosphataseBone Morphogenetic Protein 2Bone Morphogenetic Protein 4CalciumCell DifferentiationCell ProliferationCells, CulturedChemokine CCL27ChildDental PulpHumansMaleModels, BiologicalNeurofibromatosis 1OsteocalcinOsteogenesisAlkaline PhosphataseBMP2 protein, humanBMP4 protein, humanBone Morphogenetic Protein 2Bone Morphogenetic Protein 4CalciumCCL27 protein, humanChemokine CCL27OsteocalcinOsteopontinRNA, Messenger

Identifiers

PMID25480698
OpenAlexW2011337600

What OpenQuestion holds

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Registered trials

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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.