FASN expression, angiogenesis and lymphangiogenesis in central and peripheral giant cell lesions

Detalhes bibliográficos
Autor(a) principal: FALCI,Saulo Gabriel Moreira
Data de Publicação: 2014
Outros Autores: MESQUITA,Ana Terezinha Marques, ANDRADE,Bruno Augusto Benevenuto de, MIRANDA,Joao Luiz de, LEÓN,Jorge Esquiche, ALMEIDA,Oslei Paes de, SANTOS,Cássio Roberto Rocha dos
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Journal of applied oral science (Online)
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1678-77572014000200131
Resumo: Central giant cell lesion (CGCL) and peripheral giant cell lesion (PGCL) are non-neoplastic proliferative processes of the jaws. PGCL is a reactive process induced by irritant local factors and CGCL is an intra-osseous lesion of unknown etiology. Both lesions exhibit similar histologic features showing abundant mononuclear cells, admixed with a large number of multinucleated giant cells and a rich vascularized stroma with extravasated erythrocytes, hemosiderin deposition, and blood-filled pools. Recent studies have linked fatty acid synthase (FASN) with angiogenesis. Objective: To evaluate angiogenesis and lymphangiogenesis and their relationship with FASN expression in CGCL and PGCL. Material and Methods: Thirteen CGCL and 14 PGCL of the jaws were selected for immunoexpression of FASN; CD34 and CD105 (to assess blood microvessel density [MVD] and microvessel area [MVA]); and D2-40 (to assess lymphatic MVD and MVA). Results: Within PGCL and CGCL, MVD-CD34 was signifcantly higher than MVD-CD10S, followed by MVD-D2-40. Moreover, a signifcantly higher number of FASN-positive multinucleated giant cells than mononuclear cells were observed. Between PGCL and CGCL, only MVD-CD34 and all MVA were signifcantly higher in PGCL. Positive correlation between MVA-CD10S with FASNpositive mononuclear cells in both lesions was observed. Conclusions: Our results show both lesions exhibiting similar levels of FASN expression and neoangiogenesis, suggesting constitutive processes that regulate tissue maintenance.
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spelling FASN expression, angiogenesis and lymphangiogenesis in central and peripheral giant cell lesionsGiant cell lesionImmunohistochemistryAngiogenesisLymphangiogenesisFatty acid synthaseCentral giant cell lesion (CGCL) and peripheral giant cell lesion (PGCL) are non-neoplastic proliferative processes of the jaws. PGCL is a reactive process induced by irritant local factors and CGCL is an intra-osseous lesion of unknown etiology. Both lesions exhibit similar histologic features showing abundant mononuclear cells, admixed with a large number of multinucleated giant cells and a rich vascularized stroma with extravasated erythrocytes, hemosiderin deposition, and blood-filled pools. Recent studies have linked fatty acid synthase (FASN) with angiogenesis. Objective: To evaluate angiogenesis and lymphangiogenesis and their relationship with FASN expression in CGCL and PGCL. Material and Methods: Thirteen CGCL and 14 PGCL of the jaws were selected for immunoexpression of FASN; CD34 and CD105 (to assess blood microvessel density [MVD] and microvessel area [MVA]); and D2-40 (to assess lymphatic MVD and MVA). Results: Within PGCL and CGCL, MVD-CD34 was signifcantly higher than MVD-CD10S, followed by MVD-D2-40. Moreover, a signifcantly higher number of FASN-positive multinucleated giant cells than mononuclear cells were observed. Between PGCL and CGCL, only MVD-CD34 and all MVA were signifcantly higher in PGCL. Positive correlation between MVA-CD10S with FASNpositive mononuclear cells in both lesions was observed. Conclusions: Our results show both lesions exhibiting similar levels of FASN expression and neoangiogenesis, suggesting constitutive processes that regulate tissue maintenance. Faculdade De Odontologia De Bauru - USP2014-04-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S1678-77572014000200131Journal of Applied Oral Science v.22 n.2 2014reponame:Journal of applied oral science (Online)instname:Universidade de São Paulo (USP)instacron:USP10.1590/1678-775720130509info:eu-repo/semantics/openAccessFALCI,Saulo Gabriel MoreiraMESQUITA,Ana Terezinha MarquesANDRADE,Bruno Augusto Benevenuto deMIRANDA,Joao Luiz deLEÓN,Jorge EsquicheALMEIDA,Oslei Paes deSANTOS,Cássio Roberto Rocha doseng2014-03-31T00:00:00Zoai:scielo:S1678-77572014000200131Revistahttp://www.scielo.br/jaosPUBhttps://old.scielo.br/oai/scielo-oai.php||jaos@usp.br1678-77651678-7757opendoar:2014-03-31T00:00Journal of applied oral science (Online) - Universidade de São Paulo (USP)false
dc.title.none.fl_str_mv FASN expression, angiogenesis and lymphangiogenesis in central and peripheral giant cell lesions
title FASN expression, angiogenesis and lymphangiogenesis in central and peripheral giant cell lesions
spellingShingle FASN expression, angiogenesis and lymphangiogenesis in central and peripheral giant cell lesions
FALCI,Saulo Gabriel Moreira
Giant cell lesion
Immunohistochemistry
Angiogenesis
Lymphangiogenesis
Fatty acid synthase
title_short FASN expression, angiogenesis and lymphangiogenesis in central and peripheral giant cell lesions
title_full FASN expression, angiogenesis and lymphangiogenesis in central and peripheral giant cell lesions
title_fullStr FASN expression, angiogenesis and lymphangiogenesis in central and peripheral giant cell lesions
title_full_unstemmed FASN expression, angiogenesis and lymphangiogenesis in central and peripheral giant cell lesions
title_sort FASN expression, angiogenesis and lymphangiogenesis in central and peripheral giant cell lesions
author FALCI,Saulo Gabriel Moreira
author_facet FALCI,Saulo Gabriel Moreira
MESQUITA,Ana Terezinha Marques
ANDRADE,Bruno Augusto Benevenuto de
MIRANDA,Joao Luiz de
LEÓN,Jorge Esquiche
ALMEIDA,Oslei Paes de
SANTOS,Cássio Roberto Rocha dos
author_role author
author2 MESQUITA,Ana Terezinha Marques
ANDRADE,Bruno Augusto Benevenuto de
MIRANDA,Joao Luiz de
LEÓN,Jorge Esquiche
ALMEIDA,Oslei Paes de
SANTOS,Cássio Roberto Rocha dos
author2_role author
author
author
author
author
author
dc.contributor.author.fl_str_mv FALCI,Saulo Gabriel Moreira
MESQUITA,Ana Terezinha Marques
ANDRADE,Bruno Augusto Benevenuto de
MIRANDA,Joao Luiz de
LEÓN,Jorge Esquiche
ALMEIDA,Oslei Paes de
SANTOS,Cássio Roberto Rocha dos
dc.subject.por.fl_str_mv Giant cell lesion
Immunohistochemistry
Angiogenesis
Lymphangiogenesis
Fatty acid synthase
topic Giant cell lesion
Immunohistochemistry
Angiogenesis
Lymphangiogenesis
Fatty acid synthase
description Central giant cell lesion (CGCL) and peripheral giant cell lesion (PGCL) are non-neoplastic proliferative processes of the jaws. PGCL is a reactive process induced by irritant local factors and CGCL is an intra-osseous lesion of unknown etiology. Both lesions exhibit similar histologic features showing abundant mononuclear cells, admixed with a large number of multinucleated giant cells and a rich vascularized stroma with extravasated erythrocytes, hemosiderin deposition, and blood-filled pools. Recent studies have linked fatty acid synthase (FASN) with angiogenesis. Objective: To evaluate angiogenesis and lymphangiogenesis and their relationship with FASN expression in CGCL and PGCL. Material and Methods: Thirteen CGCL and 14 PGCL of the jaws were selected for immunoexpression of FASN; CD34 and CD105 (to assess blood microvessel density [MVD] and microvessel area [MVA]); and D2-40 (to assess lymphatic MVD and MVA). Results: Within PGCL and CGCL, MVD-CD34 was signifcantly higher than MVD-CD10S, followed by MVD-D2-40. Moreover, a signifcantly higher number of FASN-positive multinucleated giant cells than mononuclear cells were observed. Between PGCL and CGCL, only MVD-CD34 and all MVA were signifcantly higher in PGCL. Positive correlation between MVA-CD10S with FASNpositive mononuclear cells in both lesions was observed. Conclusions: Our results show both lesions exhibiting similar levels of FASN expression and neoangiogenesis, suggesting constitutive processes that regulate tissue maintenance.
publishDate 2014
dc.date.none.fl_str_mv 2014-04-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1678-77572014000200131
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1678-77572014000200131
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/1678-775720130509
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv text/html
dc.publisher.none.fl_str_mv Faculdade De Odontologia De Bauru - USP
publisher.none.fl_str_mv Faculdade De Odontologia De Bauru - USP
dc.source.none.fl_str_mv Journal of Applied Oral Science v.22 n.2 2014
reponame:Journal of applied oral science (Online)
instname:Universidade de São Paulo (USP)
instacron:USP
instname_str Universidade de São Paulo (USP)
instacron_str USP
institution USP
reponame_str Journal of applied oral science (Online)
collection Journal of applied oral science (Online)
repository.name.fl_str_mv Journal of applied oral science (Online) - Universidade de São Paulo (USP)
repository.mail.fl_str_mv ||jaos@usp.br
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