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Intraperitoneal delivery of a small interfering RNA targeting NEDD1 prolongs the survival of scirrhous gastric cancer model mice

机译:靶向NEDD1的小干扰RNA的腹膜内递送延长乳糜胃癌模型小鼠的存活

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摘要

The prognosis of patients with advanced diffuse‐type gastric cancer (GC), especially scirrhous gastric cancer (SGC) remains extremely poor. Peritoneal carcinomatosis is a frequent form of metastasis of SGC. With survival rates of patients with peritoneal metastasis at 3 and 5 years being only 9.8% and 0%, respectively, development of a new treatment is urgently crucial. For such development, the establishment of a therapeutic mouse model is required. Among the 11 GC cell lines we examined, HSC‐60 showed the most well‐preserved expression profiles of the Hedgehog and epithelial‐mesenchymal transition pathways found in primary SGCs. After six cycles of harvest of ascitic tumor cells and their orthotopic inoculation in scid mice, a highly metastatic subclone of HSC‐60, 60As6 was obtained, by means of which we successfully developed peritoneal metastasis model mice. The mice treated with small interfering (si) RNA targeting NEDD1, which encodes a gamma‐tubulin ring complex‐binding protein, by the atelocollagen‐mediated delivery system showed a significantly prolonged survival. Our mouse model could thus be useful for the development of a new therapeutic modality. Intraperitoneal administration of siRNAs of targeted genes such as NEDD1 could provide a new opportunity in the treatment of the peritoneal metastasis of SGC.
机译:晚期弥漫性胃癌(GC),尤其是乳糜胃癌(SGC)患者的预后仍然极差。腹膜癌症是SGC的常见形式的转移。随着腹膜转移的患者的生存率分别仅为9.8%和0%,开发新的治疗是迫切至无要的。对于这种发展,需要建立治疗鼠标模型。在我们检查的11个GC细胞系中,HSC-60显示了在原发性SGC中发现的刺猬和上皮间充质转换途径的最良好保存的表达谱。在SCITM肿瘤细胞的六个收获六个循环之后,通过其成功地发展腹膜转移模型小鼠,获得HSC-60,60As6的高度转移亚克隆的次六循环。用小型干扰(Si)RNA处理的小鼠,其通过Atelocollagen介导的递送系统编码γ-小蛋白环复合蛋白的NEDD1,其延长了延长的存活率。因此,我们的小鼠模型可能对新的治疗方式的发展有用。腹膜内施用靶向基因如NEDD1的靶向基因,可以在治疗SGC的腹膜转移方面提供新的机会。

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