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Acute hypoxia induces upregulation of microRNA-210 expression in glioblastoma spheroids

机译:急性缺氧诱导胶质母细胞瘤球状体中microRNA-210表达的上调

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Aim: Tumor hypoxia and presence of tumor stem cells are related to therapeutic resistance and tumorigenicity in glioblastomas. The aim of the present study was therefore to identify microRNAs deregulated in acute hypoxia and to identify possible associated changes in stem cell markers. Materials & methods: Glioblastoma spheroid cultures were grown in either 2 or 21% oxygen. Subsequently, miRNA profiling was performed and expression of ten stem cell markers was examined. Results: MiRNA-210 was significantly upregulated in hypoxia in patient-derived spheroids. The stem cell markers displayed a complex regulatory pattern. Conclusion: MiRNA-210 appears to be upregulated in hypoxia in immature glioblastoma cells. This miRNA may represent a therapeutic target although it is not clear from the results whether this miRNA may be related to specific cancer stem cell functions.
机译:目的:肿瘤缺氧和肿瘤干细胞的存在与胶质母细胞瘤中的治疗性抗性和致瘤性有关。 因此,本研究的目的是鉴定在急性缺氧中管制的微小RNA,并鉴定干细胞标志物中可能的相关变化。 材料与方法:在2或21%的氧中生长胶质母细胞瘤球状培养物。 随后,进行miRNA分析,检查10个干细胞标志物的表达。 结果:MiRNA-210在患者衍生的球状体中缺氧显着上调。 干细胞标记显示复杂的调节模式。 结论:MiRNA-210似乎在未成熟的胶质母细胞瘤细胞中缺氧中的上调。 该miRNA可以代表治疗靶标,尽管该MiRNA的结果尚不清楚是否可能与特异性癌症干细胞功能有关。

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