Review
Oncogene (2007) 26, 7809–7815; doi:10.1038/sj.onc.1210878
Glioblastoma multiforme: the role of DSB repair between genotype and phenotype
1Department of Human Genetics, Saarland University, Homburg/Saar, Germany
Correspondence: Dr E Meese, Department of Human Genetics, Saarland University, Building 60, Homburg/Saar 66421, Germany. E-mail: hgemee@uniklinik-saarland.de
Abstract
Glioblastoma is the most frequent primary brain tumor in adults. The average survival time of less than 1 year did not improve notably over the last three decades. The dismal prognosis of glioblastoma patients is largely due to the striking radioresistance of this tumor. Here, we attempt a combined view on the genetics, the repair mechanisms and the radioresistance of glioblastoma. Specifically, we address the role of DNA-PKcs and the novel potential end-joining factor KUB3 in maintaining the radioresistant phenotype, the interrelationship between genetic lesions and repair mechanisms, and new perspectives that emerge from the identification of glioblastoma stem cells.
Keywords:
gene amplification, XRCC6BP1, temozolomide
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