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NEAT1 siRNA Packed with Chitosan Nanoparticles Regulates the Development of Colon Cancer Cells via lncRNA NEAT1/miR-377-3p Axis

机译:用壳聚糖纳米粒子包装的Neat1 siRNA通过LNCRNA Neat1 / miR-377-3P轴调节结肠癌细胞的发育

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摘要

This study was for verifying that transfecting colon cancer cells (CCCs) with lncRNA NEAT1 packed with siRNA chitosan nanoparticles (CNPs) can suppress lncRNA NEAT1 and biological behaviors of the cells. siRNA targeting lncRNA NEAT1 expression vector was constructed and then transfected into CCCs after being packed with CNPs. Subsequently, the impact of the transfection on biological behaviors of the cells was evaluated. As a result, with high expression in CCCs, NEAT1 was negatively bound up with miR-377-3p in cases with colon cancer (CC), and dual luciferase reporter assay confirmed the potential binding region. Additionally, after downregulating NEAT1 in CCCs, transfection of NEAT1 siRNA packed with CNPs brought a great inhibition on cell proliferation and a promotion on apoptosis, and inhibiting miR-377-3p was able to offset the role of silencing NEAT1 in CCCs. Therefore, in our opinion, NEAT1 siRNA packed with CNPs can hinder the growth and metastasis of CCCs by knocking down NEAT1 in CC, and its mechanism may be achieved by targeting miR-377-3p, which offers a novel direction for treating CC.
机译:这项研究是用于验证转染结肠癌细胞(CCCS)与lncRNA利落包装用siRNA壳聚糖纳米颗粒(CNPS)可以抑制lncRNA利落和细胞生物学行为。靶的siRNA构建lncRNA利落的表达载体,然后被填充有CNPS后转染到核心承诺。随后,对细胞生物学行为的转染的影响进行了评估。其结果是,与核心承诺高表达,利落呈负的miR-377-3p与结肠癌(CC),以及双萤光素酶报告子测定的情况下包扎证实了潜在的结合区域。另外,在幼儿中心下调利落后,利落的siRNA转染挤满了CNPS带来对细胞增殖很大的抑制和对细胞凋亡的一个推广,抑制miR-377-3p能够抵消幼儿中心沉默利落的作用。因此,在我们看来,利落的siRNA填充有CNPS可以通过在CC撞倒利落妨碍幼儿中心的生长和转移,其机制可能通过靶向来实现的miR-377-3p,它提供了用于治疗CC的新颖方向。

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