Sheng Li, Zhang Shanjuan, Xu Hui
Department of Clinical Laboratory, Yantai Yu-Huang-Ding Hospital, Yantai, Shandong, China (mainland).
Department of Imaging, People's Hospital of Rizhao, Rizhao, Shandong, China (mainland).
Med Sci Monit. 2017 Jan 10;23:138-143. doi: 10.12659/msm.902725.
BACKGROUND Slug has been found to promote migration and invasion of many cancer cells, including anaplastic thyroid cancer (ATC). Thus, targeting Slug expression could provide new approaches for the treatment of patients with ATC. MATERIAL AND METHODS Small interfering RNA (siRNA) targeting Slug (Slug siRNA) was used to construct clonal derivatives in the metastatic ATC SW1736 cells. Slug cDNA transfection was used to restore the Slug expression in the Slug siRNA-transfected SW1736 cells (Slug siRNA/SW1736). E-cadherin siRNA was used to inhibit E-cadherin expression in the Slug siRNA/SW1736 cells. The SW1736 cell migration, invasion, and signaling pathway was analyzed in vitro. Furthermore, the stable Slug siRNA-transfected SW1736 clones were used for the lung metastasis assay in an in vivo mouse model. RESULTS Targeting Slug expression in SW1736 cells showed a 45% decrease in migration and an 85% decrease in invasiveness in vitro. Knockdown of E-cadherin by E-cadherin siRNA transfection or Slug overexpression by Slug cDNA transfection restored the invasive and migrative ability in SW1736 cells. In addition, we found an 80% decrease in the number of macroscopic lung metastases nodes of mice by in vivo analysis. Western blot assay showed that Slug expression was inhibited and E-cadherin expression was increased in the Slug siRNA-transfected tumors. CONCLUSIONS Targeting Slug signaling pathway is effective in preventing lung metastasis in ATC.
已发现Slug可促进包括间变性甲状腺癌(ATC)在内的多种癌细胞的迁移和侵袭。因此,靶向Slug表达可为ATC患者的治疗提供新方法。
使用靶向Slug的小干扰RNA(siRNA)(Slug siRNA)在转移性ATC SW1736细胞中构建克隆衍生物。通过Slug cDNA转染来恢复Slug siRNA转染的SW1736细胞(Slug siRNA/SW1736)中的Slug表达。使用E-钙黏蛋白siRNA抑制Slug siRNA/SW1736细胞中的E-钙黏蛋白表达。在体外分析SW1736细胞的迁移、侵袭和信号通路。此外,将稳定转染Slug siRNA的SW1736克隆用于体内小鼠模型的肺转移试验。
在SW1736细胞中靶向Slug表达显示体外迁移减少45%,侵袭性降低85%。通过E-钙黏蛋白siRNA转染敲低E-钙黏蛋白或通过Slug cDNA转染过表达Slug可恢复SW1736细胞的侵袭和迁移能力。此外,通过体内分析发现小鼠的宏观肺转移结节数量减少了80%。蛋白质印迹分析显示,在转染Slug siRNA的肿瘤中,Slug表达受到抑制,E-钙黏蛋白表达增加。
靶向Slug信号通路可有效预防ATC的肺转移。