FASN expression, angiogenesis and lymphangiogenesis in central and peripheral giant cell lesions
Autor(a) principal: | |
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Data de Publicação: | 2014 |
Outros Autores: | , , , , , |
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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USP-17 |
network_name_str |
Journal of applied oral science (Online) |
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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 |
_version_ |
1748936438074834944 |