Department of Neuropathology, Heinrich-Heine-University, Düsseldorf, Germany.
Brain Pathol. 2010 May;20(3):539-50. doi: 10.1111/j.1750-3639.2009.00328.x. Epub 2009 Sep 19.
Diffuse astrocytoma of World Health Organization (WHO) grade II has an inherent tendency to spontaneously progress to anaplastic astrocytoma WHO grade III or secondary glioblastoma WHO grade IV. We explored the role of microRNAs (miRNAs) in glioma progression by investigating the expression profiles of 157 miRNAs in four patients with primary WHO grade II gliomas that spontaneously progressed to WHO grade IV secondary glioblastomas. Thereby, we identified 12 miRNAs (miR-9, miR-15a, miR-16, miR-17, miR-19a, miR-20a, miR-21, miR-25, miR-28, miR-130b, miR-140 and miR-210) showing increased expression, and two miRNAs (miR-184 and miR-328) showing reduced expression upon progression. Validation experiments on independent series of primary low-grade and secondary high-grade astrocytomas confirmed miR-17 and miR-184 as promising candidates, which were selected for functional analyses. These studies revealed miRNA-specific influences on the viability, proliferation, apoptosis and invasive growth properties of A172 and T98G glioma cells in vitro. Using mRNA and protein expression profiling, we identified distinct sets of transcripts and proteins that were differentially expressed after inhibition of miR-17 or overexpression of miR-184 in glioma cells. Taken together, our results support an important role of altered miRNA expression in gliomas, and suggest miR-17 and miR-184 as interesting candidates contributing to glioma progression.
弥漫性脑星形细胞瘤(世界卫生组织 [WHO] 分级 II)具有自发进展为间变性星形细胞瘤(WHO 分级 III)或继发性胶质母细胞瘤(WHO 分级 IV)的固有倾向。我们通过研究 4 名原发性 WHO 分级 II 脑胶质瘤患者的 miRNA 表达谱,探讨了 miRNA 在胶质瘤进展中的作用,这些患者的肿瘤自发进展为 WHO 分级 IV 继发性胶质母细胞瘤。因此,我们确定了 12 个 miRNA(miR-9、miR-15a、miR-16、miR-17、miR-19a、miR-20a、miR-21、miR-25、miR-28、miR-130b、miR-140 和 miR-210)表达上调,2 个 miRNA(miR-184 和 miR-328)表达下调。在独立的原发性低级别和继发性高级别星形细胞瘤系列中进行的验证实验证实了 miR-17 和 miR-184 是很有前途的候选物,随后对其进行了功能分析。这些研究揭示了 miRNA 对 A172 和 T98G 神经胶质瘤细胞体外活力、增殖、凋亡和侵袭生长特性的特异性影响。利用 mRNA 和蛋白质表达谱分析,我们确定了在抑制 miR-17 或过表达 miR-184 后,胶质瘤细胞中差异表达的不同转录本和蛋白质集。总之,我们的研究结果支持 miRNA 表达改变在胶质瘤中的重要作用,并表明 miR-17 和 miR-184 是促进胶质瘤进展的有趣候选物。