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首页> 外文期刊>Brain research >Identification of MMP-9 specific microRNA expression profile as potential targets of anti-invasion therapy in glioblastoma multiforme.
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Identification of MMP-9 specific microRNA expression profile as potential targets of anti-invasion therapy in glioblastoma multiforme.

机译:鉴定MMP-9特异性microRNA表达谱作为多形性胶质母细胞瘤抗侵袭治疗的潜在目标。

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摘要

The poor prognosis of glioblastoma multiforme (GBM) is largely attributed to their highly invasive nature and MMP-9 plays a pivotal role in regulating invasiveness of malignant glioma cells. MicroRNAs (miRNAs) are small non-coding RNAs that have been shown to regulate a wide range of biological processes via targeting messenger RNA. Previous reports have shown many oncogenes regulate survival and invasion via targeting MMP-9 in GBM. But no literature indicates that miRNAs regulate glioma cell invasion through targeting MMP-9. Here, we show MMP-9 overexpression conferred a poor prognosis in 163 GBM patients. Furthermore, MMP-9 specific miRNA expression profile (14 positively and 31 negatively correlated miRNAs with MMP-9) was established via miRNA microarrays in 60 GBM samples. Among them, two miRNAs: miR-885-5p and miR-491-5p, were chosen for functional validation for their high positive correlation with MMP-9 expression. And upregulation of miR-885-5p and miR-491-5p were demonstrated to reduce the levels of MMP-9 expression and inhibit cellular invasion in U251 and U87 glioma cells. Furthermore, we found that miR-491-5p suppressed glioma cell invasion via targeting MMP-9 directly. To our knowledge, this is the first study to identify the MMP-9 specific microRNA signature which may provide potential targets for anti-invasion therapy in GBM.
机译:多形性胶质母细胞瘤(GBM)的预后不良主要归因于其高度侵袭性,MMP-9在调节恶性神经胶质瘤细胞的侵袭性中起关键作用。 MicroRNA(miRNA)是小的非编码RNA,已被证明可通过靶向信使RNA来调节广泛的生物过程。先前的报道表明,许多致癌基因通过靶向GBM中的MMP-9来调节生存和侵袭。但没有文献表明miRNA通过靶向MMP-9调节神经胶质瘤细胞的侵袭。在这里,我们显示MMP-9过表达在163 GBM患者中预后不良。此外,通过miRNA芯片在60 GBM样品中建立了MMP-9特异性miRNA表达谱(与MMP-9正相关的14个miRNA和31个负相关的miRNA)。其中,选择了两个miRNA:miR-885-5p和miR-491-5p用于功能验证,因为它们与MMP-9表达高度正相关。并且证明miR-885-5p和miR-491-5p的上调可降低U251和U87胶质瘤细胞中MMP-9的表达水平并抑制细胞侵袭。此外,我们发现miR-491-5p通过直接靶向MMP-9抑制了胶质瘤细胞的侵袭。据我们所知,这是鉴定MMP-9特异性microRNA标志的第一项研究,该标志可能为GBM中的抗侵袭治疗提供潜在的靶标。

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