O6-Methylguanine-DNA methyltransferase protein expression by immunohistochemistry in brain and non-brain systemic tumours: systematic review and meta-analysis of correlation with methylation-specific polymerase chain reaction

Background: The DNA repair protein O-6-Methylguanine-DNA methyltransferase (MGMT) confers resistance to alkylating agents. Several methods have been applied to its analysis, with methylation-specific polymerase chain reaction (MSP) the most commonly used for promoter methylation study, while immunoh...

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Detalhes bibliográficos
Autores: Brell Doval, Marta, Ibáñez Domínguez, Javier Angel, Tortosa, Avelina
Formato: artículo
Fecha de publicación:2011
País:España
Recursos:Conselleria de Salut i Consum del Govern de les Illes Balears
Repositorio:Docusalut
Idioma:inglés
OAI Identifier:oai:docusalut.com:20.500.13003/13385
Acesso em linha:https://hdl.handle.net/20.500.13003/13385
Access Level:acceso abierto
Palavra-chave:Prognosis
Neoplasms
Brain Neoplasms
O(6)-Methylguanine-DNA Methyltransferase
Polymerase Chain Reaction
Humans
Immunohistochemistry
DNA Methylation
Promoter Regions, Genetic
Reacción en Cadena de la Polimerasa
Neoplasias
Humanos
O(6)-Metilguanina-ADN Metiltransferasa
Regiones Promotoras Genéticas
Metilación de ADN
Neoplasias Encefálicas
Inmunohistoquímica
Pronóstico
Descrição
Resumo:Background: The DNA repair protein O-6-Methylguanine-DNA methyltransferase (MGMT) confers resistance to alkylating agents. Several methods have been applied to its analysis, with methylation-specific polymerase chain reaction (MSP) the most commonly used for promoter methylation study, while immunohistochemistry (IHC) has become the most frequently used for the detection of MGMT protein expression. Agreement on the best and most reliable technique for evaluating MGMT status remains unsettled. The aim of this study was to perform a systematic review and meta-analysis of the correlation between IHC and MSP. Methods: A computer-aided search of MEDLINE (1950-October 2009), EBSCO (1966-October 2009) and EMBASE (1974-October 2009) was performed for relevant publications. Studies meeting inclusion criteria were those comparing MGMT protein expression by IHC with MGMT promoter methylation by MSP in the same cohort of patients. Methodological quality was assessed by using the QUADAS and STARD instruments. Previously published guidelines were followed for meta-analysis performance. Results: Of 254 studies identified as eligible for full-text review, 52 (20.5%) met the inclusion criteria. The review showed that results of MGMT protein expression by IHC are not in close agreement with those obtained with MSP. Moreover, type of tumour (primary brain tumour vs others) was an independent covariate of accuracy estimates in the meta-regression analysis beyond the cut-off value. Conclusions: Protein expression assessed by IHC alone fails to reflect the promoter methylation status of MGMT. Thus, in attempts at clinical diagnosis the two methods seem to select different groups of patients and should not be used interchangeably.