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Evaluation of therapeutic effect of targeting nanobubbles conjugated with NET-1 siRNA by shear wave elastography: an in vivo study of hepatocellular carcinoma bearing mice model

机译:剪切波弹性成像技术评估靶向NET-1 siRNA的纳米气泡的治疗效果:肝细胞癌小鼠模型的体内研究

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This study aimed at investigating the tumor stiffness of hepatocellular carcinoma (HCC) bearing mice model in vivo to evaluate the therapeutic efficacy of targeting nanobubbles (TNBS) conjugated with NET-1 siRNA (NET-1 siRNA-TNBS). Also tested whether shear wave elastography (SWE) could demonstrate the pathological tumor changes and used to monitor therapeutic efficacy as a noninvasive method. The HCC bearing mice model was established by injecting human HCC cell line (HepG2). The mice were then divided into three groups randomly, and were treated with TNBS conjugated with NET-1 siRNA, TNBS conjugated with negative control gene, and saline as control. US-SWE was performed for three times. SWE values of all the tumors in three groups were increased with tumor growth. Emax was correlated with tumor size (p??.05). NET-1 gene (treatment group) significantly delayed the growth of tumor size compared to other two groups (p??.0001), showing a significantly increased Emax (p??.05). Immunohistochemical results showed that the NET-1 protein expression was significantly lower than the negative control and blank groups. In conclusion, TNBS conjugated with NET-1 siRNA inhibited tumor growth and prolonged the life of experimental animals. SWE provided a noninvasive and real time imaging method to detect the changes in tumor development.
机译:这项研究的目的是在体内研究肝细胞癌(HCC)小鼠模型的肿瘤僵硬度,以评估靶向与NET-1 siRNA(NET-1 siRNA-TNBS)共轭的纳米气泡(TNBS)的治疗效果。还测试了剪切波弹性成像(SWE)是否可以证明病理性肿瘤的变化并用作非侵入性方法来监测治疗效果。通过注射人HCC细胞系(HepG2)建立具有HCC的小鼠模型。然后将小鼠随机分为三组,并用与NET-1 siRNA缀合的TNBS,与阴性对照基因缀合的TNBS和生理盐水作为对照。 US-SWE进行了3次。随着肿瘤的生长,三组所有肿瘤的SWE值均升高。 Emax与肿瘤大小相关(p≤<0.05)。与其他两组相比,NET-1基因(治疗组)显着延迟了肿瘤大小的生长(p 。0001),表明Emax显着增加(p 。0.05)。免疫组织化学结果显示,NET-1蛋白表达明显低于阴性对照组和空白组。总之,与NET-1 siRNA缀合的TNBS抑制了肿瘤的生长并延长了实验动物的寿命。 SWE提供了一种非侵入性的实时成像方法来检测肿瘤发展的变化。

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