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Identification of regions correlating MGMT promoter methylation and gene expression in glioblastomas.

Authors :
Everhard S
Tost J
El Abdalaoui H
Crinière E
Busato F
Marie Y
Gut IG
Sanson M
Mokhtari K
Laigle-Donadey F
Hoang-Xuan K
Delattre JY
Thillet J
Source :
Neuro-oncology [Neuro Oncol] 2009 Aug; Vol. 11 (4), pp. 348-56. Date of Electronic Publication: 2009 Feb 17.
Publication Year :
2009

Abstract

The O(6)-methylguanine-DNA methyltransferase gene (MGMT) is methylated in several cancers, including gliomas. However, the functional role of cysteine-phosphate-guanine (CpG) island (CGI) methylation in MGMT silencing is still controversial. The aim of this study was to investigate whether MGMT CGI methylation correlates inversely with RNA expression of MGMT in glioblastomas and to determine the CpG region whose methylation best reflects the level of expression. The methylation level of CpG sites that are potentially related to expression was investigated in 54 glioblastomas by pyrosequencing, a highly quantitative method, and analyzed with respect to their MGMT mRNA expression status. Three groups of patients were identified according to the methylation pattern of all 52 analyzed CpG sites. Overall, an 85% rate of concordance was observed between methylation and expression (p < 0.0001). When analyzing each CpG separately, six CpG sites were highly correlated with expression (p < 0.0001), and two CpG regions could be used as surrogate markers for RNA expression in 81.5% of the patients. This study indicates that there is good statistical agreement between MGMT methylation and expression, and that some CpG regions better reflect MGMT expression than do others. However, if transcriptional repression is the key mechanism in explaining the higher chemosensitivity of MGMT-methylated tumors, a substantial rate of discordance should lead clinicians to be cautious when deciding on a therapeutic strategy based on MGMT methylation status alone.

Details

Language :
English
ISSN :
1522-8517
Volume :
11
Issue :
4
Database :
MEDLINE
Journal :
Neuro-oncology
Publication Type :
Academic Journal
Accession number :
19224763
Full Text :
https://doi.org/10.1215/15228517-2009-001