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MiR-1180-5p regulates apoptosis of Wilms’ tumor by targeting p73

机译:MiR-1180-5p通过靶向 p 73调控Wilms肿瘤的凋亡

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Introduction: Wilms’ tumor (WT), the most common childhood tumor, occurs in sporadic or familial forms. Recent findings reported that abnormal expression in microRNA (miRNA) suggests an important role of miRNAs during WT progress. MiRNAs are endogenous short-chain noncoding RNAs, which have been reported as key biomarkers for detecting tumor onset and progression. However, the functional role of miR-1180 in WT has remained unknown. Materials and methods: MTT and clonogenic survival assays were used to detect WT cell proliferation. Flow cytometry Annexin V-FITC was used to measure apoptosis. In addition, proteins expressions in the cells were determined by Western blotting. Results: In the present study, we demonstrated that miR-1180 is upregulated in WT when compared with adjacent tissues by quantitative reverse-transcription polymerase chain reaction. In addition, the inhibition of miR-1180 induced apoptosis in SK-NEP-1 cell line in vitro. Moreover, luciferase reporter assay showed that p 73 protein was the target of miR-1180, which was confirmed by the results of Western blotting. Finally, in vivo data indicated that the tumor growth in mice was significantly inhibited by miR-1180 inhibitor. Conclusion: Our results indicate that miR-1180 might serve as a therapeutic target for future WT therapy.
机译:简介:Wilms肿瘤(WT)是儿童中最常见的肿瘤,以散发或家族形式出现。最近的发现报道,microRNA(miRNA)中的异常表达表明miRNA在WT进展中的重要作用。 MiRNA是内源性的短链非编码RNA,已报道它们是检测肿瘤发作和进展的关键生物标志物。但是,miR-1180在野生型中的功能作用仍然未知。材料和方法:MTT和克隆形成存活测定法用于检测WT细胞增殖。流式细胞仪Annexin V-FITC用于测量细胞凋亡。另外,通过蛋白质印迹法测定细胞中的蛋白质表达。结果:在本研究中,我们证明了通过定量逆转录聚合酶链反应与相邻组织相比,miR-1180在野生型中被上调。此外,miR-1180的抑制在体外诱导SK-NEP-1细胞系凋亡。此外,荧光素酶报告基因测定显示p 73蛋白是miR-1180的靶标,这已通过蛋白质印迹法的证实。最后,体内数据表明miR-1180抑制剂可显着抑制小鼠的肿瘤生长。结论:我们的结果表明miR-1180可能成为未来WT治疗的治疗靶标。

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