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Abundant immunohistochemical expression of dopamine D(2) receptor and p53 protein in meningiomas: follow-up, relation to gender, age, tumor grade, and recurrence

Meningiomas are common, usually benign tumors, with a high postoperative recurrence rate. However, the genesis and development of these tumors remain controversial. We aimed to investigate the presence and implications of a mutated p53 protein and dopamine D(2) receptor in a representative series of...

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Autores principales: Trott, G., Pereira-Lima, J.F.S., Leães, C.G.S., Ferreira, N.P., Barbosa-Coutinho, L.M., Oliveira, M.C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Associação Brasileira de Divulgação Científica 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4445664/
https://www.ncbi.nlm.nih.gov/pubmed/25742638
http://dx.doi.org/10.1590/1414-431X20144163
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author Trott, G.
Pereira-Lima, J.F.S.
Leães, C.G.S.
Ferreira, N.P.
Barbosa-Coutinho, L.M.
Oliveira, M.C.
author_facet Trott, G.
Pereira-Lima, J.F.S.
Leães, C.G.S.
Ferreira, N.P.
Barbosa-Coutinho, L.M.
Oliveira, M.C.
author_sort Trott, G.
collection PubMed
description Meningiomas are common, usually benign tumors, with a high postoperative recurrence rate. However, the genesis and development of these tumors remain controversial. We aimed to investigate the presence and implications of a mutated p53 protein and dopamine D(2) receptor in a representative series of meningiomas and to correlate these findings with age, gender, tumor grade, and recurrence. Tumor tissue samples of 157 patients diagnosed with meningioma (37 males and 120 females, mean age 53.6±14.3 years) who underwent surgical resection between 2003 and 2012 at our institution were immunohistochemically evaluated for the presence of p53 protein and dopamine D(2) receptor and were followed-up to analyze tumor recurrence or regrowth. Tumors were classified as grades I (n=141, 89.8%), II (n=13, 8.3%), or grade III (n=3, 1.9%). Dopamine D(2) receptor and p53 protein expression were positive in 93.6% and 49.7% of the cases, respectively. Neither of the markers showed significant expression differences among different tumor grades or recurrence or regrowth statuses. Our findings highlight the potential role of p53 protein in meningioma development and/or progression. The high positivity of dopamine D(2) receptor observed in this study warrants further investigation of the therapeutic potential of dopamine agonists in the evolution of meningiomas.
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spelling pubmed-44456642015-06-08 Abundant immunohistochemical expression of dopamine D(2) receptor and p53 protein in meningiomas: follow-up, relation to gender, age, tumor grade, and recurrence Trott, G. Pereira-Lima, J.F.S. Leães, C.G.S. Ferreira, N.P. Barbosa-Coutinho, L.M. Oliveira, M.C. Braz J Med Biol Res Biomedical Sciences Meningiomas are common, usually benign tumors, with a high postoperative recurrence rate. However, the genesis and development of these tumors remain controversial. We aimed to investigate the presence and implications of a mutated p53 protein and dopamine D(2) receptor in a representative series of meningiomas and to correlate these findings with age, gender, tumor grade, and recurrence. Tumor tissue samples of 157 patients diagnosed with meningioma (37 males and 120 females, mean age 53.6±14.3 years) who underwent surgical resection between 2003 and 2012 at our institution were immunohistochemically evaluated for the presence of p53 protein and dopamine D(2) receptor and were followed-up to analyze tumor recurrence or regrowth. Tumors were classified as grades I (n=141, 89.8%), II (n=13, 8.3%), or grade III (n=3, 1.9%). Dopamine D(2) receptor and p53 protein expression were positive in 93.6% and 49.7% of the cases, respectively. Neither of the markers showed significant expression differences among different tumor grades or recurrence or regrowth statuses. Our findings highlight the potential role of p53 protein in meningioma development and/or progression. The high positivity of dopamine D(2) receptor observed in this study warrants further investigation of the therapeutic potential of dopamine agonists in the evolution of meningiomas. Associação Brasileira de Divulgação Científica 2015-03-03 /pmc/articles/PMC4445664/ /pubmed/25742638 http://dx.doi.org/10.1590/1414-431X20144163 Text en http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Biomedical Sciences
Trott, G.
Pereira-Lima, J.F.S.
Leães, C.G.S.
Ferreira, N.P.
Barbosa-Coutinho, L.M.
Oliveira, M.C.
Abundant immunohistochemical expression of dopamine D(2) receptor and p53 protein in meningiomas: follow-up, relation to gender, age, tumor grade, and recurrence
title Abundant immunohistochemical expression of dopamine D(2) receptor and p53 protein in meningiomas: follow-up, relation to gender, age, tumor grade, and recurrence
title_full Abundant immunohistochemical expression of dopamine D(2) receptor and p53 protein in meningiomas: follow-up, relation to gender, age, tumor grade, and recurrence
title_fullStr Abundant immunohistochemical expression of dopamine D(2) receptor and p53 protein in meningiomas: follow-up, relation to gender, age, tumor grade, and recurrence
title_full_unstemmed Abundant immunohistochemical expression of dopamine D(2) receptor and p53 protein in meningiomas: follow-up, relation to gender, age, tumor grade, and recurrence
title_short Abundant immunohistochemical expression of dopamine D(2) receptor and p53 protein in meningiomas: follow-up, relation to gender, age, tumor grade, and recurrence
title_sort abundant immunohistochemical expression of dopamine d(2) receptor and p53 protein in meningiomas: follow-up, relation to gender, age, tumor grade, and recurrence
topic Biomedical Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4445664/
https://www.ncbi.nlm.nih.gov/pubmed/25742638
http://dx.doi.org/10.1590/1414-431X20144163
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