Artigo

Epigenetic alterations in human brain tumors in a Brazilian population

Aberrant methylation of CpG islands located in promoter regions represents one of the major mechanisms for silencing cancer-related genes in tumor cells. We determined the frequency of aberrant CpG island methylation for several tumor-associated genes: DAPK, MGMT, p14ARF, p16INK4a, TP73, RB1 and TIM...

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Autor principal: ANSELMO, Nilson Praia
Outros Autores: BELLO, Maria Josefa, GONZALEZ-GOMEZ, Pilar, DIAS, Luis Antonio Araújo, ALMEIDA, José Reinaldo Walter de, SANTOS, Marcelo José dos, HERRANZ, Juan Antonio Rey, CASARTELLI, Cacilda
Grau: Artigo
Idioma: por
Publicado em: 2014
Assuntos:
Acesso em linha: http://repositorio.ufpa.br/jspui/handle/2011/5961
id ir-2011-5961
recordtype dspace
spelling ir-2011-59612023-11-21T15:55:47Z Epigenetic alterations in human brain tumors in a Brazilian population ANSELMO, Nilson Praia BELLO, Maria Josefa GONZALEZ-GOMEZ, Pilar DIAS, Luis Antonio Araújo ALMEIDA, José Reinaldo Walter de SANTOS, Marcelo José dos HERRANZ, Juan Antonio Rey CASARTELLI, Cacilda Epigenética Tumores cerebrais Neoplasias encefálicas Metilação Câncer Meningioma Pará - Estado Amazônia brasileira Aberrant methylation of CpG islands located in promoter regions represents one of the major mechanisms for silencing cancer-related genes in tumor cells. We determined the frequency of aberrant CpG island methylation for several tumor-associated genes: DAPK, MGMT, p14ARF, p16INK4a, TP73, RB1 and TIMP-3 in 55 brain tumors, consisting of 26 neuroepithelial tumors, 6 peripheral nerve tumors, 13 meningeal tumors and 10 metastatic brain tumors. Aberrant methylation of at least one of the seven genes studied was detected in 83.6% of the cases. The frequencies of aberrant methylation were: 40% for p14ARF, 38.2% for MGMT, 30.9% for, p16INK4a, 14.6% for TP73 and for TIMP-3, 12.7% for DAPK and 1.8% for RB1. These data suggest that the hypermethylation observed in the genes p14ARF, MGMT and p16INK4a is a very important event in the formation or progression of brain tumors, since the inactivation of these genes directly interferes with the cell cycle or DNA repair. The altered methylation rate of the other genes has already been reported to be related to tumorigenesis, but the low methylation rate of RB1 found in tumors in our sample is different from that so far reported in the literature, suggesting that perhaps hypermethylation of the promoter is not the main event in the inactivation of this gene. Our results suggest that hypermethylation of the promoter region is a very common event in nervous system tumors. 2014-10-31T14:31:15Z 2014-10-31T14:31:15Z 2006 Artigo de Periódico ANSELMO, Nilson Praia et al. Epigenetic alterations in human brain tumors in a Brazilian population. Genetics and Molecular Biology, São Paulo, v. 29, n. 3, p. 413-422, 2006. Disponível em: <http://www.scielo.br/pdf/gmb/v29n3/30742.pdf>. Acesso em: 07 jul. 2014. <http://dx.doi.org/10.1590/S1415-47572006000300001>. 1415-4757 http://repositorio.ufpa.br/jspui/handle/2011/5961 por Acesso Aberto application/pdf
institution Repositório Institucional - Universidade Federal do Pará
collection RI-UFPA
language por
topic Epigenética
Tumores cerebrais
Neoplasias encefálicas
Metilação
Câncer
Meningioma
Pará - Estado
Amazônia brasileira
spellingShingle Epigenética
Tumores cerebrais
Neoplasias encefálicas
Metilação
Câncer
Meningioma
Pará - Estado
Amazônia brasileira
ANSELMO, Nilson Praia
Epigenetic alterations in human brain tumors in a Brazilian population
topic_facet Epigenética
Tumores cerebrais
Neoplasias encefálicas
Metilação
Câncer
Meningioma
Pará - Estado
Amazônia brasileira
description Aberrant methylation of CpG islands located in promoter regions represents one of the major mechanisms for silencing cancer-related genes in tumor cells. We determined the frequency of aberrant CpG island methylation for several tumor-associated genes: DAPK, MGMT, p14ARF, p16INK4a, TP73, RB1 and TIMP-3 in 55 brain tumors, consisting of 26 neuroepithelial tumors, 6 peripheral nerve tumors, 13 meningeal tumors and 10 metastatic brain tumors. Aberrant methylation of at least one of the seven genes studied was detected in 83.6% of the cases. The frequencies of aberrant methylation were: 40% for p14ARF, 38.2% for MGMT, 30.9% for, p16INK4a, 14.6% for TP73 and for TIMP-3, 12.7% for DAPK and 1.8% for RB1. These data suggest that the hypermethylation observed in the genes p14ARF, MGMT and p16INK4a is a very important event in the formation or progression of brain tumors, since the inactivation of these genes directly interferes with the cell cycle or DNA repair. The altered methylation rate of the other genes has already been reported to be related to tumorigenesis, but the low methylation rate of RB1 found in tumors in our sample is different from that so far reported in the literature, suggesting that perhaps hypermethylation of the promoter is not the main event in the inactivation of this gene. Our results suggest that hypermethylation of the promoter region is a very common event in nervous system tumors.
format Artigo
author ANSELMO, Nilson Praia
author2 BELLO, Maria Josefa
GONZALEZ-GOMEZ, Pilar
DIAS, Luis Antonio Araújo
ALMEIDA, José Reinaldo Walter de
SANTOS, Marcelo José dos
HERRANZ, Juan Antonio Rey
CASARTELLI, Cacilda
author2Str BELLO, Maria Josefa
GONZALEZ-GOMEZ, Pilar
DIAS, Luis Antonio Araújo
ALMEIDA, José Reinaldo Walter de
SANTOS, Marcelo José dos
HERRANZ, Juan Antonio Rey
CASARTELLI, Cacilda
title Epigenetic alterations in human brain tumors in a Brazilian population
title_short Epigenetic alterations in human brain tumors in a Brazilian population
title_full Epigenetic alterations in human brain tumors in a Brazilian population
title_fullStr Epigenetic alterations in human brain tumors in a Brazilian population
title_full_unstemmed Epigenetic alterations in human brain tumors in a Brazilian population
title_sort epigenetic alterations in human brain tumors in a brazilian population
publishDate 2014
url http://repositorio.ufpa.br/jspui/handle/2011/5961
_version_ 1832603642899726336
score 11.755432