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High expression of XIAP and Bcl-2 may inhibit programmed cell death in glioblastomas
2017
Arquivos de Neuro-Psiquiatria
Glioblastoma (GBM) is the most malignant glioma and represents 29% of all brain tumors. Tumorigenesis is intimately connected with characteristics acquired in the physiologic pathway of cellular death. Objective: In the present study, the expression of anti-apoptotic (XIAP and Bcl-2) and apoptotic (cytochrome C, caspase 9, APAF-1), caspase 3 and the Smac/DIABLO genes related to the apoptosis pathway were evaluated in 30 samples of glioblastoma. Methods: The gene expression was evaluated in 30
doi:10.1590/0004-282x20170156
pmid:29236891
fatcat:ulwwtmrsbraujcead4ac4l2ty4