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Shared
oligodendrocyte lineage gene expression in gliomas and oligodendrocyte
progenitor cells
Bouvier C, Bartoli C,
Aguirre-Cruz L, Virard I, Colin C, Fernandez C, Gouvernet J, Figarella-Branger D
Laboratoire des Interactions Neurone-Glie, Groupe Hospitalier
Pitie-Salpetriere, Paris, France
Object.
Gliomas (astrocytic and oligodendroglial) are the most frequently occurring
primary neoplasms in the central nervous system (CNS).
Histological classification, which can be performed to distinguish astrocytomas
from oligodendrogliomas, is essentially based on pathological features and has
great prognostic and therapeutic value but lacks reproducibility.
Specific markers of cell lineage, especially those for oligodendrogliomas, are
still lacking.
The oligodendrocyte lineage (OLIG) genes, transcriptional factors of the basic
helix-loop-helix family, have been recently identified in oligodendrocyte
progenitor cells (OPCs) in the CNS of developing and adult rodents.
Data from a few studies have shown in a small series of brain tumors that OLIG
genes characterize oligodendrogliomas.
To search for a differential expression of the OLIG genes in subgroups of brain
tumors, the authors investigated OLIG1 and OLIG2 gene expression.
Methods.
Using semiquantitative reverse transcription-polymerase chain reaction (RT-PCR),
the authors analyzed a series of 89 tumors (71 astrocytic and oligodendroglial
tumors, eight ependymomas, three medulloblastomas, four meningiomas, and three
schwannomas) and normal human brain tissue samples.
It was demonstrated that OLIG gene expression was largely limited to glial
tumors, that is, astrocytomas and oligodendrogliomas.
A very low level was detected in ependymomas, whereas other tumors lacked OLIG
gene expression altogether.
Surprisingly, OLIG1 and OLIG2 expression was not limited to oligodendroglial
tumors, but was observed in astrocytic lesions as well, independent of tumor
grade.
Interestingly, these genes were expressed at the highest level in pilocytic
astrocytomas according to semiquantitative RT-PCR results, which were confirmed
on dot blot analysis.
In situ hybridization showed that the OLIG2 gene was expressed by tumor cells in
pilocytic astrocytomas as well as those in oligodendrogliomas.
Conclusions.
The OLIG genes are additional markers shared by all gliomas and OPCs.
These markers may help to classify gliomas, to improve understanding of their
histogenesis, and to identify new therapeutic targets.
PMID: 12924709 [PubMed - in process]
Source: http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=12924709&dopt=Abstract
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