Neuropathology and Applied Neurobiology · 2007 · 36 citations · 38 references
MedicineOncologyPathologyGlial BiologyNeuro-oncologyTumor HeterogeneityBrain TumorsGlial Cell BiologyGlial DevelopmentGlial Gene ExpressionGlioblastomaNeuro-oncologic PathologyDevelopmental Transcription FactorsGlioblastoma BiomarkersGlioblastoma Molecular SubtypesGlioblastoma PathologyIntermediate Filament OrganizationIntermediate Filament-associated ProteinsOligodendroglioma PathologyProteolipid Protein
In order to define specific markers for histogenesis of three well-characterized subgroups of human gliomas (pilocytic astrocytomas, glioblastoma multiforme and oligodendrogliomas), we studied the expression of relevant markers that characterize gliomagenesis, by immunohistochemistry and in situ hybridization. They include the intermediate filament proteins glial fibrillary acidic protein (GFAP), vimentin and nestin, the transcription factors Olig2, Nkx2.2 and Sox10, and the proteolipid protein transcripts plp/dm20. We show that the three major categories of human gliomas express a combinatorial profile of markers that gives new insights to their histogenesis and may help diagnosis. Pilocytic astrocytomas strongly express GFAP, vimentin, Olig2, Nkx2.2 and Sox10 but not nestin. In contrast, glioblastomas strongly express GFAP, vimentin and nestin but these tumours are heterogeneous regarding the expression of the transcription factors studied. Finally, in oligodendrogliomas, intermediate filament proteins are generally not observed whereas Olig2 was found in almost all tumour cells nuclei while only a subpopulation of tumour cells expressed Nkx2.2 and Sox10.
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Identification of human brain tumour initiating cells
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