SuicidDentistV1, Main, Exploration, bibRecord, 000153

Immunoexpression of Glucose Transporters 1 and 3 and Macrophage Colony-Stimulating Factor in Central and Peripheral Giant Cell Lesions of the Jaws.

Identifieur interne : 000153 ( Main/Exploration ); précédent : 000152; suivant : 000154

Immunoexpression of Glucose Transporters 1 and 3 and Macrophage Colony-Stimulating Factor in Central and Peripheral Giant Cell Lesions of the Jaws.

Auteurs : Rodrigo Gadelha Vasconcelos [Brésil] ; Felipe Rodrigues De Matos [Brésil] ; Marcelo Gadelha Vasconcelos [Brésil] ; Anderson Nicolly Fernandes Da Costa [Brésil] ; Lélia Maria Guedes Queiroz [Brésil]

Source :

Journal of oral and maxillofacial surgery : official journal of the American Association of Oral and Maxillofacial Surgeons [ 1531-5053 ] ; 2016.

RBID : pubmed:26706492

Descripteurs français

English descriptors

KwdEn :
- Giant Cells (metabolism), Glucose Transporter Type 1 (metabolism), Glucose Transporter Type 1 (physiology), Glucose Transporter Type 3 (metabolism), Glucose Transporter Type 3 (physiology), Granuloma, Giant Cell (metabolism), Granuloma, Giant Cell (pathology), Humans (MeSH), Jaw Diseases (metabolism), Jaw Diseases (pathology), Leukocytes, Mononuclear (metabolism), Macrophage Colony-Stimulating Factor (metabolism), Macrophage Colony-Stimulating Factor (physiology).
MESH :
- chemical , metabolism : Glucose Transporter Type 1, Glucose Transporter Type 3, Macrophage Colony-Stimulating Factor.
- metabolism : Giant Cells, Granuloma, Giant Cell, Jaw Diseases, Leukocytes, Mononuclear.
- pathology : Granuloma, Giant Cell, Jaw Diseases.
- chemical , physiology : Glucose Transporter Type 1, Glucose Transporter Type 3, Macrophage Colony-Stimulating Factor.
- Humans.

Abstract

PURPOSE

The peripheral giant cell lesion (PGCL) is a reactive process associated with a local irritating factor that shows low recurrence after treatment, especially if the irritating factor is eliminated. In contrast, the central giant cell lesion (CGCL) presents variable clinical behavior ranging from slow and asymptomatic growth without recurrence to rapid, painful, and recurrent growth. The immunoexpression of glucose transporter (GLUT)-1, GLUT-3, and macrophage colony-stimulating factor (M-CSF) was compared in CGCL and PGCL.

MATERIALS AND METHODS

Twenty nonaggressive CGCLs, 20 aggressive CGCLs, and 20 PGCLs were selected for analysis of the immunoexpression of GLUT-1, GLUT-3, and M-CSF in multinuclear giant cells (MGCs) and mononuclear cells (MCs).

RESULTS

There was a difference in the percentage of immunoreactive cells of GLUT-1 and GLUT-3 in MC components among lesions and in the intensity of GLUT-1 in MCG and MC components, GLUT-3 in MGC components, and M-CSF in MC components.

CONCLUSIONS

These results suggest that GLUT-1, GLUT-3, and M-CSF could play a role in the pathogenesis of the lesions studied. The stronger immunostaining of these proteins in MCs shows that these cells have greater metabolic activity and osteoclastogenesis, especially in aggressive CGCL. The MCs showed a stronger relation than the MGCs to the pathogenesis of the studied lesions.

DOI: 10.1016/j.joms.2015.11.022
PubMed: 26706492

Affiliations:

Links toward previous steps (curation, corpus...)

to stream Main, to step Corpus: 000158
to stream Main, to step Curation: 000158

Le document en format XML

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<term>Glucose Transporter Type 1 (metabolism)</term>
<term>Glucose Transporter Type 1 (physiology)</term>
<term>Glucose Transporter Type 3 (metabolism)</term>
<term>Glucose Transporter Type 3 (physiology)</term>
<term>Granuloma, Giant Cell (metabolism)</term>
<term>Granuloma, Giant Cell (pathology)</term>
<term>Humans (MeSH)</term>
<term>Jaw Diseases (metabolism)</term>
<term>Jaw Diseases (pathology)</term>
<term>Leukocytes, Mononuclear (metabolism)</term>
<term>Macrophage Colony-Stimulating Factor (metabolism)</term>
<term>Macrophage Colony-Stimulating Factor (physiology)</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr"><term>Agranulocytes (métabolisme)</term>
<term>Cellules géantes (métabolisme)</term>
<term>Facteur de stimulation des colonies de macrophages (métabolisme)</term>
<term>Facteur de stimulation des colonies de macrophages (physiologie)</term>
<term>Granulome à cellules géantes (anatomopathologie)</term>
<term>Granulome à cellules géantes (métabolisme)</term>
<term>Humains (MeSH)</term>
<term>Maladies de la mâchoire (anatomopathologie)</term>
<term>Maladies de la mâchoire (métabolisme)</term>
<term>Transporteur de glucose de type 1 (métabolisme)</term>
<term>Transporteur de glucose de type 1 (physiologie)</term>
<term>Transporteur de glucose de type 3 (métabolisme)</term>
<term>Transporteur de glucose de type 3 (physiologie)</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="metabolism" xml:lang="en"><term>Glucose Transporter Type 1</term>
<term>Glucose Transporter Type 3</term>
<term>Macrophage Colony-Stimulating Factor</term>
</keywords>
<keywords scheme="MESH" qualifier="anatomopathologie" xml:lang="fr"><term>Granulome à cellules géantes</term>
<term>Maladies de la mâchoire</term>
</keywords>
<keywords scheme="MESH" qualifier="metabolism" xml:lang="en"><term>Giant Cells</term>
<term>Granuloma, Giant Cell</term>
<term>Jaw Diseases</term>
<term>Leukocytes, Mononuclear</term>
</keywords>
<keywords scheme="MESH" qualifier="métabolisme" xml:lang="fr"><term>Agranulocytes</term>
<term>Cellules géantes</term>
<term>Facteur de stimulation des colonies de macrophages</term>
<term>Granulome à cellules géantes</term>
<term>Maladies de la mâchoire</term>
<term>Transporteur de glucose de type 1</term>
<term>Transporteur de glucose de type 3</term>
</keywords>
<keywords scheme="MESH" qualifier="pathology" xml:lang="en"><term>Granuloma, Giant Cell</term>
<term>Jaw Diseases</term>
</keywords>
<keywords scheme="MESH" qualifier="physiologie" xml:lang="fr"><term>Facteur de stimulation des colonies de macrophages</term>
<term>Transporteur de glucose de type 1</term>
<term>Transporteur de glucose de type 3</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="physiology" xml:lang="en"><term>Glucose Transporter Type 1</term>
<term>Glucose Transporter Type 3</term>
<term>Macrophage Colony-Stimulating Factor</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Humans</term>
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<front><div type="abstract" xml:lang="en"><p><b>PURPOSE</b>
</p>
<p>The peripheral giant cell lesion (PGCL) is a reactive process associated with a local irritating factor that shows low recurrence after treatment, especially if the irritating factor is eliminated. In contrast, the central giant cell lesion (CGCL) presents variable clinical behavior ranging from slow and asymptomatic growth without recurrence to rapid, painful, and recurrent growth. The immunoexpression of glucose transporter (GLUT)-1, GLUT-3, and macrophage colony-stimulating factor (M-CSF) was compared in CGCL and PGCL.</p>
</div>
<div type="abstract" xml:lang="en"><p><b>MATERIALS AND METHODS</b>
</p>
<p>Twenty nonaggressive CGCLs, 20 aggressive CGCLs, and 20 PGCLs were selected for analysis of the immunoexpression of GLUT-1, GLUT-3, and M-CSF in multinuclear giant cells (MGCs) and mononuclear cells (MCs).</p>
</div>
<div type="abstract" xml:lang="en"><p><b>RESULTS</b>
</p>
<p>There was a difference in the percentage of immunoreactive cells of GLUT-1 and GLUT-3 in MC components among lesions and in the intensity of GLUT-1 in MCG and MC components, GLUT-3 in MGC components, and M-CSF in MC components.</p>
</div>
<div type="abstract" xml:lang="en"><p><b>CONCLUSIONS</b>
</p>
<p>These results suggest that GLUT-1, GLUT-3, and M-CSF could play a role in the pathogenesis of the lesions studied. The stronger immunostaining of these proteins in MCs shows that these cells have greater metabolic activity and osteoclastogenesis, especially in aggressive CGCL. The MCs showed a stronger relation than the MGCs to the pathogenesis of the studied lesions.</p>
</div>
</front>
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<Abstract><AbstractText Label="PURPOSE" NlmCategory="OBJECTIVE">The peripheral giant cell lesion (PGCL) is a reactive process associated with a local irritating factor that shows low recurrence after treatment, especially if the irritating factor is eliminated. In contrast, the central giant cell lesion (CGCL) presents variable clinical behavior ranging from slow and asymptomatic growth without recurrence to rapid, painful, and recurrent growth. The immunoexpression of glucose transporter (GLUT)-1, GLUT-3, and macrophage colony-stimulating factor (M-CSF) was compared in CGCL and PGCL.</AbstractText>
<AbstractText Label="MATERIALS AND METHODS" NlmCategory="METHODS">Twenty nonaggressive CGCLs, 20 aggressive CGCLs, and 20 PGCLs were selected for analysis of the immunoexpression of GLUT-1, GLUT-3, and M-CSF in multinuclear giant cells (MGCs) and mononuclear cells (MCs).</AbstractText>
<AbstractText Label="RESULTS" NlmCategory="RESULTS">There was a difference in the percentage of immunoreactive cells of GLUT-1 and GLUT-3 in MC components among lesions and in the intensity of GLUT-1 in MCG and MC components, GLUT-3 in MGC components, and M-CSF in MC components.</AbstractText>
<AbstractText Label="CONCLUSIONS" NlmCategory="CONCLUSIONS">These results suggest that GLUT-1, GLUT-3, and M-CSF could play a role in the pathogenesis of the lesions studied. The stronger immunostaining of these proteins in MCs shows that these cells have greater metabolic activity and osteoclastogenesis, especially in aggressive CGCL. The MCs showed a stronger relation than the MGCs to the pathogenesis of the studied lesions.</AbstractText>
<CopyrightInformation>Copyright © 2016. Published by Elsevier Inc.</CopyrightInformation>
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<name sortKey="Vasconcelos, Marcelo Gadelha" sort="Vasconcelos, Marcelo Gadelha" uniqKey="Vasconcelos M" first="Marcelo Gadelha" last="Vasconcelos">Marcelo Gadelha Vasconcelos</name>
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   |texte=   Immunoexpression of Glucose Transporters 1 and 3 and Macrophage Colony-Stimulating Factor in Central and Peripheral Giant Cell Lesions of the Jaws.
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	Serveur d'exploration sur le suicide chez les dentistes
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Serveur d'exploration sur le suicide chez les dentistes

Immunoexpression of Glucose Transporters 1 and 3 and Macrophage Colony-Stimulating Factor in Central and Peripheral Giant Cell Lesions of the Jaws.

Immunoexpression of Glucose Transporters 1 and 3 and Macrophage Colony-Stimulating Factor in Central and Peripheral Giant Cell Lesions of the Jaws.

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