...
首页> 外文期刊>The journal of clinical investigation >p90 ribosomal S6 kinase 2 promotes invasion and metastasis of human head and neck squamous cell carcinoma cells
【24h】

p90 ribosomal S6 kinase 2 promotes invasion and metastasis of human head and neck squamous cell carcinoma cells

机译:p90核糖体S6激酶2促进人头颈部鳞状细胞癌细胞的侵袭和转移

获取原文

摘要

Head and neck squamous cell carcinoma (HNSCC) is one of the most common types of human cancer and frequently metastasizes to LNs. Identifying metastasis-promoting factors is of immense clinical interest, as the prognosis for patients with even a single unilateral LN metastasis is extremely poor. Here, we report that p90 ribosomal S6 kinase 2 (RSK2) promotes human HNSCC cell invasion and metastasis. We determined that RSK2 was overexpressed and activated in highly invasive HNSCC cell lines compared with poorly invasive cell lines. Expression of RSK2 also correlated with metastatic progression in patients with HNSCC. Ectopic expression of RSK2 substantially enhanced the invasive capacity of HNSCC cells, while inhibition of RSK2 activity led to marked attenuation of invasion in vitro. Additionally, shRNA knockdown of RSK2 substantially reduced the invasive and metastatic potential of HNSCC cells in vitro and in vivo in a xenograft mouse model, respectively. Mechanistically, we determined that cAMP-responsive element-binding protein (CREB) and Hsp27 are phosphorylated and activated by RSK2 and are important for the RSK2-mediated invasive ability of HNSCC cells. Our findings suggest that RSK2 is involved in the prometastatic programming of HNSCC cells, through phosphorylation of proteins in a putative signaling network. Moreover, targeting RSK2 markedly attenuates in vitro invasion and in vivo metastasis of HNSCC cells, suggesting that RSK2 may represent a therapeutic target in the treatment of metastatic HNSCC.
机译:头颈部鳞状细胞癌(HNSCC)是人类最常见的癌症类型之一,并经常转移至LNs。确定转移促进因子具有巨大的临床意义,因为即使是单侧LN转移患者的预后也非常差。在这里,我们报道p90核糖体S6激酶2(RSK2)促进人类HNSCC细胞侵袭和转移。我们确定与低侵袭性细胞系相比,RSK2在高侵袭性HNSCC细胞系中过表达和激活。 RSK2的表达也与HNSCC患者的转移进展有关。 RSK2的异位表达大大增强了HNSCC细胞的侵袭能力,而对RSK2活性的抑制则导致体外侵袭的明显减弱。此外,在异种移植小鼠模型中,RSK2的shRNA敲低分别显着降低了HNSCC细胞在体外和体内的侵袭和转移潜力。从机理上讲,我们确定cAMP反应元件结合蛋白(CREB)和Hsp27被RSK2磷酸化和激活,并且对于RSK2介导的HNSCC细胞的侵袭能力很重要。我们的发现表明,RSK2通过推定信号网络中蛋白质的磷酸化参与HNSCC细胞的前转移编程。而且,靶向RSK2显着减弱了HNSCC细胞的体外侵袭和体内转移,这表明RSK2可能代表了转移性HNSCC的治疗靶标。

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