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MicroRNA miR-1249 downregulates adenomatous polyposis coli 2 expression and promotes glioma cells proliferation

机译:MicroRNA miR-1249下调腺瘤性息肉病大肠杆菌2的表达并促进神经胶质瘤细胞增殖

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Continuous activation of the Wnt/β-Catenin signaling has been reported to play important roles in multiple process of tumor progression, leading to uncontrolled cancer cell proliferation, growth, and survival. However, the mechanism underlying the regulation of the Wnt/β-Catenin pathway remains largely unknown. Determining the molecular mechanism of the Wnt/β-Catenin pathway’s aberrant activation in glioma carcinogenesis might improve therapeutic strategies for patients with glioma. In this study, we showed that the expression of microRNA miR-1249 was markedly upregulated in glioma cell lines and tissues. Upregulation of miR-1249 enhanced, whereas downregulation inhibited, the proliferation of glioma cells both in vitro and in vivo. Furthermore, bioinformatic and experimental approaches showed that miR-1249 targets and suppresses APC2 expression, an important Wnt/β-Catenin pathway-regulated factor. These data suggested that miR-1249 could be a novel therapeutic target of microRNA-mediated cell proliferation in glioma.
机译:据报道,Wnt /β-连环蛋白信号传导的持续激活在肿瘤进展的多个过程中起重要作用,导致不受控制的癌细胞增殖,生长和存活。但是,Wnt /β-Catenin途径调控的基本机制仍然未知。确定神经胶质瘤癌变过程中Wnt /β-连环蛋白途径异常激活的分子机制可能会改善神经胶质瘤患者的治疗策略。在这项研究中,我们表明在胶质瘤细胞系和组织中,microRNA miR-1249的表达明显上调。在体外和体内,miR-1249的上调都增强了胶质瘤细胞的增殖,而下调则抑制了。此外,生物信息学和实验方法表明,miR-1249靶向并抑制APC2表达,这是一种重要的Wnt /β-Catenin途径调控因子。这些数据表明,miR-1249可能是神经胶质瘤中microRNA介导的细胞增殖的新型治疗靶点。

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