Malignant gliomas are tumors characterized by high heterogeneity; therefore, our study used two intracranial glioma models, GL261-5 and GSC-005, to address the possibility of obtaining results due to the specific genetic makeup of a single model. The murine glioma cell line GL261-5 (a clone with slower in vivo growth kinetics compared with GL261, from the Tumor Bank Repository, National Cancer Institute, Frederick, MD, USA)23 (link) was cultured in Dulbecco’s modified Eagle’s medium with nutrient mixture F12 (DMEM/F12) (Corning). Additionally, the murine GSC-005 glioma cells (kindly provided by I.M. Verma, The Salk Institute for Biological Studies, CA, USA)61 (link) were maintained in DMEM/F12 supplemented with N2 (1×, Invitrogen), fibroblast growth factor 2 (20 ng/mL, PeproTech), epidermal growth factor (20 ng/mL, Promega), and heparin (50 μg/mL, Sigma). Cell cultures were further supplemented with 10% fetal bovine serum (HyCline Laboratories), penicillin (100 μg/mL, Corning), and streptomycin (100 μg/mL, Corning) and were stored under the following conditions: 37°C and 5% CO2.
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