| Literature DB >> 17854667 |
Magdalena Zakrzewska1, Malgorzata Szybka, Krzysztof Zakrzewski, Wojciech Biernat, Radzisław Kordek, Piotr Rieske, Ewa Golanska, Izabela Zawlik, Sylwester Piaskowski, Paweł P Liberski.
Abstract
Glioblastoma multiforme (GBM), the most common malignant brain tumor of adults, is relatively rare in children. In a GBM affecting a 16-year-old boy, the tumor spread across the corpus callosum (butterfly glioma). This type of bilateral hemispheric growth has previously been thought to result from spread along the white matter tracts. Two samples obtained from opposite sides of the same tumor were analyzed comprehensively for loss of heterozygosity (LOH) and microsatellite instability (MSI). Amplification of EGFR and MDM2 was studied by means of multiplex polymerase chain reaction. Exons 5, 6, 7, and 8 of TP53 were screened for mutations by sequencing. In neither specimen were molecular alterations found in the EGFR, MDM2, or TP53 genes. The specimen obtained from the right hemisphere exhibited a high level of MSI and LOH in chromosome arms 5q, 9p, and 13q. The specimen from the left hemisphere exhibited LOH in chromosome arms 3p, 5q, 9p, 9q, 10p, 10q, and 13q. Here we propose four plausible hypothetical scenarios underlying the tumorigenesis of this GBM.Entities:
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Year: 2007 PMID: 17854667 DOI: 10.1016/j.cancergencyto.2007.04.019
Source DB: PubMed Journal: Cancer Genet Cytogenet ISSN: 0165-4608