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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

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dc.creator Brell Doval, Marta
dc.creator Ibáñez, Javier
dc.creator Tortosa i Moreno, Avelina
dc.date 2011-06-08T10:04:56Z
dc.date 2011-06-08T10:04:56Z
dc.date 2011-01-26
dc.date 2011-02-15T17:08:05Z
dc.date.accessioned 2024-12-16T10:26:08Z
dc.date.available 2024-12-16T10:26:08Z
dc.identifier 1471-2407
dc.identifier http://hdl.handle.net/2445/18324
dc.identifier 589752
dc.identifier 21269507
dc.identifier.uri http://fima-docencia.ub.edu:8080/xmlui/handle/123456789/20565
dc.description Background: The DNA repair protein O6-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.
dc.format 13 p.
dc.format application/pdf
dc.language eng
dc.publisher BioMed Central
dc.relation Reproducció del document publicat a: http://dx.doi.org/10.1186/1471-2407-11-35
dc.relation BMC Cancer, 2011, vol. 11, núm. 35
dc.relation http://dx.doi.org/10.1186/1471-2407-11-35
dc.rights cc-by, (c) Brell et al., 2011
dc.rights http://creativecommons.org/licenses/by/2.0/
dc.rights Brell et al.; licensee BioMed Central Ltd.
dc.rights info:eu-repo/semantics/openAccess
dc.source Articles publicats en revistes (Infermeria Fonamental i Clínica)
dc.subject Expressió gènica
dc.subject Immunohistoquímica
dc.subject Cervell
dc.subject Gene expression
dc.subject Immunohistochemistry
dc.subject Brain
dc.title 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
dc.type info:eu-repo/semantics/article
dc.type info:eu-repo/semantics/publishedVersion


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