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MiR-876-3p targets KIF20A to block JAK2/STAT3 pathway in glioma

机译:MiR-876-3p靶向KIF20A阻断神经胶质瘤的JAK2 / STAT3途径

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摘要

Aberrant expression of miRNAs has been reported to be involved in the development and progression of glioma. But the function of miR-876-3p in glioma is unknown. We found that miR-876-3p is significantly downregulated in glioma tissues and cell lines. Overexpression of miR-876-3p suppressed glioma cell proliferation, epithelial-mesenchymal transition, migration, and invasion. By prediction combining with luciferase reporter assay, we identified that miR-876-3p could decrease the expression of KIF20A by directly targeting the region of its 3’UTR. Furthermore, we observed that overexpression of miR-876-3p inhibited the expression of KIF20A, thus blocking the protein kinase JAK2/STAT3 pathway. Overexpressed KIF20A reversed miR-876-3p-induced suppression of glioma cell proliferation, migration, and invasion. We also demonstrated the inhibitory effect of miR-876-3p on tumor growth in glioma using an in vivo model. The miR-876-3p/KIF20A-axis mediated JAK2/STAT3 pathway have therapeutic potential in glioma treatment.
机译:据报道,miRNA的异常表达与神经胶质瘤的发生和发展有关。但是,miR-876-3p在神经胶质瘤中的功能尚不清楚。我们发现,miR-876-3p在神经胶质瘤组织和细胞系中显着下调。 miR-876-3p的过表达抑制神经胶质瘤细胞增殖,上皮-间质转化,迁移和侵袭。通过预测与荧光素酶报告基因检测相结合,我们确定了miR-876-3p可以通过直接靶向3'UTR区域来降低KIF20A的表达。此外,我们观察到miR-876-3p的过表达抑制了KIF20A的表达,从而阻断了蛋白激酶JAK2 / STAT3途径。过表达的KIF20A逆转了miR-876-3p诱导的神经胶质瘤细胞增殖,迁移和侵袭抑制。我们还证明了使用体内模型,miR-876-3p对神经胶质瘤中肿瘤生长的抑制作用。 miR-876-3p / KIF20A轴介导的JAK2 / STAT3途径在神经胶质瘤治疗中具有治疗潜力。

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