LSU Neuroscience Center & Department of Ophthalmology, Louisiana State University Health Science Center, New Orleans, LA 70112, USA.
J Neurooncol. 2010 Jul;98(3):297-304. doi: 10.1007/s11060-009-0077-0. Epub 2009 Nov 26.
High density micro-RNA (miRNA) arrays, fluorescent-reporter miRNA assay and Northern miRNA dot-blot analysis show that a brain-enriched miRNA-128 is significantly down-regulated in glioblastoma multiforme (GBM) and in GBM cell lines when compared to age-matched controls. The down-regulation of miRNA-128 was found to inversely correlate with WHO tumor grade. Three bioinformatics-verified miRNA-128 targets, angiopoietin-related growth factor protein 5 (ARP5; ANGPTL6), a transcription suppressor that promotes stem cell renewal and inhibits the expression of known tumor suppressor genes involved in senescence and differentiation, Bmi-1, and a transcription factor critical for the control of cell-cycle progression, E2F-3a, were found to be up-regulated. Addition of exogenous miRNA-128 to CRL-1690 and CRL-2610 GBM cell lines (a) restored 'homeostatic' ARP5 (ANGPTL6), Bmi-1 and E2F-3a expression, and (b) significantly decreased the proliferation of CRL-1690 and CRL-2610 cell lines. Our data suggests that down-regulation of miRNA-128 may contribute to glioma and GBM, in part, by coordinately up-regulating ARP5 (ANGPTL6), Bmi-1 and E2F-3a, resulting in the proliferation of undifferentiated GBM cells.
高密度 microRNA (miRNA) 阵列、荧光报告 miRNA 检测和 Northern miRNA 点印迹分析表明,与年龄匹配的对照相比,脑丰富 miRNA-128 在多形性胶质母细胞瘤 (GBM) 和 GBM 细胞系中显著下调。miRNA-128 的下调与世界卫生组织 (WHO) 肿瘤分级呈负相关。三个经过生物信息学验证的 miRNA-128 靶标,血管生成素相关生长因子蛋白 5 (ARP5; ANGPTL6)、一种转录抑制剂,可促进干细胞更新并抑制与衰老和分化相关的已知肿瘤抑制基因的表达、Bmi-1 和一种转录因子,对于控制细胞周期进程至关重要,E2F-3a,被发现上调。将外源性 miRNA-128 添加到 CRL-1690 和 CRL-2610 GBM 细胞系中 (a) 恢复了“稳态”的 ARP5 (ANGPTL6)、Bmi-1 和 E2F-3a 的表达,(b) 显著降低了 CRL-1690 和 CRL-2610 细胞系的增殖。我们的数据表明,miRNA-128 的下调可能通过协调上调 ARP5 (ANGPTL6)、Bmi-1 和 E2F-3a 来促进胶质瘤和 GBM 的发生,从而导致未分化 GBM 细胞的增殖。