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首页> 外文期刊>Molecular cancer therapeutics >An anti-Wnt5a antibody suppresses metastasis of gastric cancer cells in vivo by inhibiting receptor-mediated endocytosis
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An anti-Wnt5a antibody suppresses metastasis of gastric cancer cells in vivo by inhibiting receptor-mediated endocytosis

机译:抗Wnt5a抗体通过抑制受体介导的内吞作用来抑制体内胃癌细胞的转移

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Wnt5a is a representative ligand that activates the β-catenin- independent pathway in Wnt signaling. It was reported that the expression of Wnt5a in human gastric cancer is associated with aggressiveness and poor prognosis and that knockdown of Wnt5a reduces the ability of gastric cancer cells to metastasize in nude mice. Therefore, Wnt5a and its signaling pathway might be important targets for the therapy of gastric cancer. The aim of this study was to examine whether an anti-Wnt5a antibody affects metastasis of gastric cancer cells. One anti-Wnt5a polyclonal antibody (pAb5a-5) inhibited migration and invasion activities in vitro of gastric cancer cells with a high expression level of Wnt5a. Previously, it was shown that Wnt5a induces the internalization of receptors, which is required for Wnt5a-dependent activation of Rac1. pAb5a-5 inhibited Wnt5a-dependent internalization of receptors, thereby suppressed Wnt5a-dependent activation of Rac1. Laminin γ2 is one of target genes of Wnt5a signaling and Rac1 was involved in its expression. pAb5a-5 also inhibited Wnt5a-dependent expression of laminin γ2. In an experimental liver metastasis assay, gastric cancer cells were introduced into the spleens of nude mice. Laminin γ2 was required for liver metastatic ability of gastric cancer cells in vivo. Furthermore, intraperitoneal injection of pAb5a-5 inhibited the metastatic ability of gastric cancer cells. These results suggest that an anti-Wnt5a antibody was capable of suppressing Wnt5a-dependent internalization of receptors, resulting in the prevention of metastasis of gastric cancer cells by inhibiting the activation of Rac1 and the expression of laminin γ2.
机译:Wnt5a是激活Wnt信号传导中β-catenin依赖性途径的代表性配体。据报道,Wnt5a在人胃癌中的表达与侵略性和预后不良有关,并且敲低Wnt5a可降低胃癌细胞在裸鼠中转移的能力。因此,Wnt5a及其信号通路可能是胃癌治疗的重要靶标。这项研究的目的是检查抗Wnt5a抗体是否影响胃癌细胞的转移。一种抗Wnt5a多克隆抗体(pAb5a-5)抑制具有高表达水平的Wnt5a的胃癌细胞的体外迁移和侵袭活性。以前,已显示Wnt5a诱导受体的内在化,这是Wnt5a依赖的Rac1激活所必需的。 pAb5a-5抑制了受体的Wnt5a依赖性内在化,从而抑制了Rac1的Wnt5a依赖性活化。层粘连蛋白γ2是Wnt5a信号转导的靶基因之一,Rac1参与其表达。 pAb5a-5还抑制层粘连蛋白γ2的Wnt5a依赖性表达。在实验性肝转移试验中,胃癌细胞被引入裸鼠的脾脏中。层粘连蛋白γ2是体内胃癌细胞肝转移能力所必需的。此外,腹膜内注射pAb5a-5抑制胃癌细胞的转移能力。这些结果表明抗Wnt5a抗体能够抑制受体的Wnt5a依赖性内在化,从而通过抑制Rac1的活化和层粘连蛋白γ2的表达来预防胃癌细胞的转移。

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