| Literature DB >> 25080476 |
Carolin Müller1, Johannes Holtschmidt2, Martina Auer3, Ellen Heitzer3, Katrin Lamszus4, Alexander Schulte4, Jakob Matschke5, Sabine Langer-Freitag6, Christin Gasch1, Malgorzata Stoupiec1, Oliver Mauermann1, Sven Peine7, Markus Glatzel5, Michael R Speicher3, Jochen B Geigl3, Manfred Westphal4, Klaus Pantel8, Sabine Riethdorf1.
Abstract
Glioblastoma multiforme (GBM) is the most frequent and aggressive brain tumor in adults. The dogma that GBM spread is restricted to the brain was challenged by reports on extracranial metastases after organ transplantation from GBM donors. We identified circulating tumor cells (CTCs) in peripheral blood (PB) from 29 of 141 (20.6%) GBM patients by immunostaining of enriched mononuclear cells with antibodies directed against glial fibrillary acidic protein (GFAP). Tumor cell spread was not significantly enhanced by surgical intervention. The tumor nature of GFAP-positive cells was supported by the absence of those cells in healthy volunteers and the presence of tumor-specific aberrations such as EGFR gene amplification and gains and losses in genomic regions of chromosomes 7 and 10. Release of CTCs was associated with EGFR gene amplification, suggesting a growth potential of these cells. We demonstrate that hematogenous GBM spread is an intrinsic feature of GBM biology.Entities:
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Year: 2014 PMID: 25080476 DOI: 10.1126/scitranslmed.3009095
Source DB: PubMed Journal: Sci Transl Med ISSN: 1946-6234 Impact factor: 17.956