Molecular genetic studies of glial tumors in children
https://doi.org/10.24884/1607-4181-2016-23-4-49-53
Abstract
Glioblastomas are the most frequent malignant neoplasm among primary brain tumors of childhood. Despite the advances in a multimodality treatment approach including neurosurgery, radiotherapy and chemotherapy, the overall survival of such patients remains poor and doesn’t exceed 14 months. The using of targeted agents such as gefitinib in unselected patient populations showed insufficient efficacy. Nowadays, the most perspective approach is a selection of patient populations potentially sensitive to targeted therapy based on predictive markers of response. We performed a comprehensive analysis of the mutational patterns in 30 glioblastomas of children. Data Analysis was based on the new method of mass spectrometry (OncoCarta v1.0, Sequenom) that enabled us to estimate 298 mutations in 19 genes and to identify 10 mutations in 9 tumors (30 %). Mutations were found in BRAF, CDK, HRAS, EGFR, FGFR, MET and PI3K. The most mutated pathway was EGFR – in 20 % of the samples (6/30). The obtained results seem to be very promising in terms of possibilities of using new targeted agents including BRAF inhibitors for treatment of children with glial brain tumors.
About the Authors
P. S. SoltanRussian Federation
F. V. Moiseenko
Russian Federation
V. N. Ochkolyas
V. Yu. Startsev
Russian Federation
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Review
For citations:
Soltan P.S., Moiseenko F.V., Ochkolyas V.N., Startsev V.Yu. Molecular genetic studies of glial tumors in children. The Scientific Notes of the Pavlov University. 2016;23(4):49-53. (In Russ.) https://doi.org/10.24884/1607-4181-2016-23-4-49-53