Immunohistochemical expression of RANKL in oral giant cell lesions is predictive of aggressiveness

Abstract The aim of this study was to evaluate the immunohistochemical expression of receptor activator of nuclear factor kappa-B ligand (RANKL) and of osteoprotegerin (OPG), important proteins correlated with osteoclastogenesis, in central giant cell lesions (CGCL) and peripheral giant cell lesions...

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Main Authors: Georgia MARTINI, Diogo CAPELLA, Elena Riet Correa RIVERO, Rogério Oliveira GONDAK
Format: Article
Language:English
Published: Sociedade Brasileira de Pesquisa Odontológica 2018-10-01
Series:Brazilian Oral Research
Subjects:
Online Access:http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1806-83242018000100291&lng=en&tlng=en
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spelling doaj-bab2068446d649e5904f6f04a0a13e702020-11-25T02:46:56ZengSociedade Brasileira de Pesquisa Odontológica Brazilian Oral Research1807-31072018-10-0132010.1590/1807-3107bor-2018.vol32.0115S1806-83242018000100291Immunohistochemical expression of RANKL in oral giant cell lesions is predictive of aggressivenessGeorgia MARTINIDiogo CAPELLAElena Riet Correa RIVERORogério Oliveira GONDAKAbstract The aim of this study was to evaluate the immunohistochemical expression of receptor activator of nuclear factor kappa-B ligand (RANKL) and of osteoprotegerin (OPG), important proteins correlated with osteoclastogenesis, in central giant cell lesions (CGCL) and peripheral giant cell lesions (PGCL) and to compare their expression with the histological and clinical parameters for quantification of multinucleated giant cells (MGC) and their nuclei, lesion size, and recurrences. Twenty cases of each lesion type were selected to quantify the number of MGCs and nuclei/mm2 of connective tissue. The immunoreactivity of RANKL and OPG was expressed as a percentage of the marked area in the stroma. Clinical data were collected from pathoanatomical and medical reports. No statistical differences were found for the number of MGCs (p = 0.24) between PGCL and CGCL, but the number of nuclei within the MGCs was higher in CGCL (p = 0.01). RANKL expression was higher in CGCL than in PGCL (p = 0.04) and all recurrent lesions showed higher RANKL and OPG expressions than nonrecurrent lesions. We report higher RANKL expression and a greater number of nuclei in CGCL, which may explain the difference in clinical behaviour between these lesions and their pathogenesis.http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1806-83242018000100291&lng=en&tlng=enNF-kappa BOsteoprotegerinImmunohistochemistry
collection DOAJ
language English
format Article
sources DOAJ
author Georgia MARTINI
Diogo CAPELLA
Elena Riet Correa RIVERO
Rogério Oliveira GONDAK
spellingShingle Georgia MARTINI
Diogo CAPELLA
Elena Riet Correa RIVERO
Rogério Oliveira GONDAK
Immunohistochemical expression of RANKL in oral giant cell lesions is predictive of aggressiveness
Brazilian Oral Research
NF-kappa B
Osteoprotegerin
Immunohistochemistry
author_facet Georgia MARTINI
Diogo CAPELLA
Elena Riet Correa RIVERO
Rogério Oliveira GONDAK
author_sort Georgia MARTINI
title Immunohistochemical expression of RANKL in oral giant cell lesions is predictive of aggressiveness
title_short Immunohistochemical expression of RANKL in oral giant cell lesions is predictive of aggressiveness
title_full Immunohistochemical expression of RANKL in oral giant cell lesions is predictive of aggressiveness
title_fullStr Immunohistochemical expression of RANKL in oral giant cell lesions is predictive of aggressiveness
title_full_unstemmed Immunohistochemical expression of RANKL in oral giant cell lesions is predictive of aggressiveness
title_sort immunohistochemical expression of rankl in oral giant cell lesions is predictive of aggressiveness
publisher Sociedade Brasileira de Pesquisa Odontológica
series Brazilian Oral Research
issn 1807-3107
publishDate 2018-10-01
description Abstract The aim of this study was to evaluate the immunohistochemical expression of receptor activator of nuclear factor kappa-B ligand (RANKL) and of osteoprotegerin (OPG), important proteins correlated with osteoclastogenesis, in central giant cell lesions (CGCL) and peripheral giant cell lesions (PGCL) and to compare their expression with the histological and clinical parameters for quantification of multinucleated giant cells (MGC) and their nuclei, lesion size, and recurrences. Twenty cases of each lesion type were selected to quantify the number of MGCs and nuclei/mm2 of connective tissue. The immunoreactivity of RANKL and OPG was expressed as a percentage of the marked area in the stroma. Clinical data were collected from pathoanatomical and medical reports. No statistical differences were found for the number of MGCs (p = 0.24) between PGCL and CGCL, but the number of nuclei within the MGCs was higher in CGCL (p = 0.01). RANKL expression was higher in CGCL than in PGCL (p = 0.04) and all recurrent lesions showed higher RANKL and OPG expressions than nonrecurrent lesions. We report higher RANKL expression and a greater number of nuclei in CGCL, which may explain the difference in clinical behaviour between these lesions and their pathogenesis.
topic NF-kappa B
Osteoprotegerin
Immunohistochemistry
url http://www.scielo.br/scielo.php?script=sci_arttext&pid=S1806-83242018000100291&lng=en&tlng=en
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AT elenarietcorrearivero immunohistochemicalexpressionofranklinoralgiantcelllesionsispredictiveofaggressiveness
AT rogeriooliveiragondak immunohistochemicalexpressionofranklinoralgiantcelllesionsispredictiveofaggressiveness
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