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microRNA-182 inhibits the proliferation and migration of glioma cells through the induction of neuritin expression

机译:microRNA-182通过诱导神经素表达抑制神经胶质瘤细胞的增殖和迁移

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摘要

Astrocytomas are the most common type of glial tumors and carry a poor prognosis. However, the pathogenesis of astrocytomas remains to be elucidated. Neuritin, a novel member of the neurotrophic factors family, has been shown to be associated with tumor malignancy, via the regulation of apoptosis and proliferation. In the present study, microRNA-182 (miR-182) was cloned and transfected into the U251 human astrocytoma cell line, in order to investigate its regulatory effects on the proliferation and migration of these cells, as well as its association with the expression of neuritin. The results showed that miR-182 specifically targets the gene encoding neuritin, NRN1, as demonstrated by a reduction in the protein and mRNA levels of NRN1. In addition, overexpression of miR-182 affected cell cycle regulation and cell migration capacity in vitro, which may have been associated with the promotion of apoptosis by this molecule. In conclusion, endogenous miR-182 may be involved in the pathogenesis of astrocytoma, which is associated with the miR-182-regulated gene, NRN1.
机译:星形细胞瘤是最常见的神经胶质瘤类型,预后较差。然而,星形细胞瘤的发病机理仍有待阐明。神经营养素是神经营养因子家族的新成员,已通过调节细胞凋亡和增殖而与肿瘤恶性肿瘤相关。在本研究中,将microRNA-182(miR-182)克隆并转染到U251人星形细胞瘤细胞系中,以研究其对这些细胞的增殖和迁移的调控作用,以及与uRNA表达的关系。神经素。结果表明,miR-182特异性靶向编码神经素NRN1的基因,这通过降低NRN1的蛋白质和mRNA水平证明。另外,miR-182的过表达在体外影响细胞周期调节和细胞迁移能力,这可能与该分子促进细胞凋亡有关。总之,内源性miR-182可能参与星形细胞瘤的发病机理,这与miR-182调控的基因NRN1有关。

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