Division of Neuropathology, Department of Pathology and Laboratory Medicine, Perelman School of Medicine, University of Pennsylvania, Philadelphia, USA.
Brain Pathol. 2012 Jul;22(4):522-9. doi: 10.1111/j.1750-3639.2011.00551.x. Epub 2011 Dec 9.
Central nervous system (CNS) tumors in von Hippel-Lindau syndrome (VHL) include hemangioblastomas and metastatic clear cell renal cell carcinomas (Met CCRCC). While these tumors often show similar histologic features, differentiating them is of significant importance as Met CCRCC are higher-grade tumors with worse prognosis. No single current immunohistochemical marker unequivocally differentiates between these two entities. MicroRNAs (miRNAs) are noncoding cellular small RNA molecules that play an important role in cancer. We hypothesized that hemangioblastomas and Met CCRCC display distinct miRNA signatures enabling their histologic differentiation. MiRNAs were profiled in 10 cases each of hemangioblastomas, Met CCRCC and primary CCRCC. Ten miRNAs had greater abundance (including miR-9 (∼10-fold) and miR-135a (∼7-fold)) and 39 miRNAs were lower [including miR-200a (∼22-fold) and miR-200b (∼12-fold)] in hemangioblastomas compared with Met CCRCC. Quantitative real-time RT-PCR in 20 hemangioblastomas and 13 Met CCRCC showed a 12-fold increase in miR-9 and a 15-fold decrease of miR-200a in hemangioblastomas compared with Met CCRCC. Finally, in situ hybridization for miR-9 in 15 hemangioblastomas and 10 Met CCRCC confirmed these results. Our data suggest that miR-9 and miR-200a can distinguish between hemangioblastomas and Met CCRCC. Further, these results may also provide insight in understanding the biology of hemangioblastomas.
中枢神经系统(CNS)肿瘤在 von Hippel-Lindau 综合征(VHL)中包括血管母细胞瘤和转移性透明细胞肾细胞癌(Met CCRCC)。虽然这些肿瘤通常表现出相似的组织学特征,但区分它们具有重要意义,因为 Met CCRCC 是高级别肿瘤,预后更差。目前没有单一的免疫组织化学标志物能够明确区分这两种实体。microRNAs(miRNAs)是一种非编码细胞小 RNA 分子,在癌症中发挥重要作用。我们假设血管母细胞瘤和 Met CCRCC 显示出不同的 miRNA 特征,使其能够进行组织学分化。对 10 例血管母细胞瘤、Met CCRCC 和原发性 CCRCC 进行 miRNA 分析。10 种 miRNA 的丰度更高(包括 miR-9(约 10 倍)和 miR-135a(约 7 倍)),39 种 miRNA 的丰度更低[包括 miR-200a(约 22 倍)和 miR-200b(约 12 倍)]与 Met CCRCC 相比,在血管母细胞瘤中。在 20 例血管母细胞瘤和 13 例 Met CCRCC 中进行的定量实时 RT-PCR 显示,与 Met CCRCC 相比,血管母细胞瘤中 miR-9 的表达增加了 12 倍,miR-200a 的表达降低了 15 倍。最后,对 15 例血管母细胞瘤和 10 例 Met CCRCC 进行 miR-9 的原位杂交证实了这些结果。我们的数据表明,miR-9 和 miR-200a 可以区分血管母细胞瘤和 Met CCRCC。此外,这些结果还可能为理解血管母细胞瘤的生物学提供深入了解。