首页> 外文期刊>Oncology reports >CCL19-induced chemokine receptor 7 activates the phosphoinositide-3 kinase-mediated invasive pathway through Cdc42 in metastatic squamous cell carcinoma of the head and neck.
【24h】

CCL19-induced chemokine receptor 7 activates the phosphoinositide-3 kinase-mediated invasive pathway through Cdc42 in metastatic squamous cell carcinoma of the head and neck.

机译:CCL19诱导的趋化因子受体7激活了头颈部转移性鳞状细胞癌中磷酸肌醇3激酶介导的通过Cdc42的侵入途径。

获取原文
获取原文并翻译 | 示例
           

摘要

Metastatic squamous cell carcinoma of the head and neck (SCCHN) has been shown to express chemokine receptor 7 (CCR7), which activates phosphoinositide-3 kinase (PI3K) to promote invasion and survival of SCCHN cells. We hypothesized that Cdc42 might be involved in the CCR7-PI3K pathway. Adhesion assays, migration assays, immunofluorescence staining, Western blotting and immunohistochemical analysis were used to find whether Cdc42 can be activated by CCL19 (the CCR7 ligand) and its role in SCCHN. Results showed that CCL19 induced polarized localization of Cdc42 and actin polymerization in the leading edge of migrating cells. The level of activated membrane-bound Cdc42 was elevated, as measured by the GTPase activity pull-down assay. The increased membrane localization and membrane-bound activity of Cdc42 were abolished by CCR7 and PI3K inhibition, indicating the involvement of Cdc42 in the CCR7-PI3K cascade. Knockdown of Cdc42 by small interfering RNA (siRNA) led to significant reduction in the activation of Rac, filamentous actin (F-actin) accumulation as well as in the migration and invasion induced by CCL19. Taken together, our data indicate the important role played by Cdc42 in CCL19-induced migration and invasion of SCCHN cells.
机译:头颈部转移性鳞状细胞癌(SCCHN)已显示表达趋化因子受体7(CCR7),后者激活磷酸肌醇3激酶(PI3K)促进SCCHN细胞的侵袭和存活。我们假设Cdc42可能参与了CCR7-PI3K途径。粘附测定,迁移测定,免疫荧光染色,蛋白质印迹和免疫组织化学分析被用于发现Cdc42是否可以被CCL19(CCR7配体)激活,以及它在SCCHN中的作用。结果表明,CCL19诱导了Cdc42的极化定位和肌动蛋白在迁移细胞前沿的聚合。如通过GTPase活性下拉测定所测量的,活化的膜结合的Cdc42的水平升高。 Cdc7和PI3K抑制作用消除了Cdc42的增加的膜定位和膜结合活性,表明Cdc42参与了CCR7-PI3K级联反应。通过小干扰RNA(siRNA)抑制Cdc42,可导致Rac的激活,丝状肌动蛋白(F-actin)积累以及CCL19诱导的迁移和侵袭显着降低。综上所述,我们的数据表明Cdc42在CCL19诱导的SCCHN细胞迁移和侵袭中发挥了重要作用。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号