作者: Tieyi Hu , Niqi Xie , Chuan Qin , Jiasheng Wang , Yi You
DOI: 10.1007/S13277-015-3635-4
关键词: Glioma 、 Cell growth 、 U87 、 Cell biology 、 Biology 、 Signal transduction 、 Wnt signaling pathway 、 LRP5 、 Cell migration 、 Gene silencing
摘要: Malignant glioma is the most common type of primary brain tumor and represents one aggressive lethal human cancer types. Glioma recurrence a event; however, relevant molecular mechanisms in this setting are not well-understood. In study, we investigated glucose-regulated protein 94 (GRP94) expressions aimed to determine roles GRP94 expression affects cell proliferation, invasion, regulatory signaling U87 cells. Our results showed that was overexpressed at both mRNA levels high-grade glioblastoma as compared with normal tissues. High also predict shorter overall survival patients. RNAi-mediated silencing suppressed cellular colony formation ability Depletion inhibited migration invasion cell. Furthermore, gene microarray analysis revealed depletion caused dysregulation critical pathway, Wnt/β-catenin pathway. We next demonstrated regulates pathway promote proliferation Conclusion, our findings establish progression markers druggable targets glioblastoma, relating their oncogenic effects activation