American Journal of Clinical Pathology · 2010 · 60 citations · 24 references
MedicineMolecular BiologyOncologyCarcinogenesisEpigeneticsMolecular OncologyCancer EpigeneticsDna MethylationDna Methylation ProfilingEpigenetic Alterations In CancerEpigenetic Regulation In CancerEpigenetic Regulation In DevelopmentAberrant Dna MethylationDna MethyltransferasesImmunohistochemical DetectionImmunohistochemical MarkersImmunohistochemical StainingMolecular Pathogenesis Of RetinoblastomaPromoter MethylationRetinoblastoma Family Proteins
DNA methyltransferases (DNMTs) 1, 3a, and 3b affect DNA promoter methylation; studies have suggested that they have important roles in the development of cancers. In this study, we analyzed the expression of DNMTs 1, 3a, and 3b; the MIB-1 labeling index; and their clinical significance in 6 normal retinas and 62 retinoblastomas using immunohistochemical analysis. We found that DNMT proteins were not expressed in normal retinas, whereas they were frequently expressed in retinoblastomas (DNMT1, 100%; DNMT3a, 98%; and DNMT3b, 92%). Compared with well-differentiated retinoblastomas, the expression of DNMTs 1 and 3a significantly increased in poorly differentiated retinoblastomas (P = .002 and P = .003, respectively); in addition, the frequency of their increased expression was high. DNMT1 expression was significantly higher in invasive retinoblastoma. Furthermore, the expression of DNMTs was positively correlated with the MIB-1 labeling index in retinoblastoma. Our findings suggest that the overexpression of DNMTs 1, 3a, and 3b may be related to retinoblastoma tumorigenesis and progression and may represent a novel approach for retinoblastoma therapy.
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