Institute of Tumor Molecular Surgery, The First Affiliated Hospital, Zhengzhou University Medical College, 40 Daxue Road, 450052, Zhengzhou, Henan, China.
Mol Biol Rep. 2010 Apr;37(4):1971-7. doi: 10.1007/s11033-009-9645-9. Epub 2009 Aug 2.
Rho-associated protein kinase (ROCK), a molecular switch, modulates cellular functions in many cancers, such as hepatocellular, breast, colon cancers, etc. However, little is known the effect of ROCK on cell adhesion and mobility in esophageal squamous cell cancer (ESCC), one of the most diagnosed cancers in China. In this study, Y-27632 was used to specifically block ROCK activity in ESCC cells. Adhesion of ESCC cells was detected by homotypic and heterotypic adhesion assay together with examination of E-cadherin expression. Motility of ESCC cells changes were examined by detection of phosphorylated cofilin and observed under confocal microscopy, respectively. We found that Y-27632 increased both heterotypic and homotypic adhesion, and the expression of E-cadherin; decreased phosphorylated cofilin resulting in actin rearrangement in ESCC cells. All these findings indicate that ROCK signaling pathway plays an important role in cell adhesion and mobility, suggesting that it may be used as a potential target for therapy of ESCC.
Rho 相关蛋白激酶(ROCK)作为一种分子开关,调节着多种癌症中的细胞功能,如肝癌、乳腺癌、结肠癌等。然而,对于 ROCK 在食管鳞状细胞癌(ESCC)中对细胞黏附和迁移的影响知之甚少,ESCC 是中国最常见的癌症之一。在这项研究中,使用 Y-27632 特异性阻断 ESCC 细胞中的 ROCK 活性。通过同质和异质黏附测定以及 E-钙黏蛋白表达的检测来检测 ESCC 细胞的黏附。通过检测磷酸化丝切蛋白和共聚焦显微镜观察来检测 ESCC 细胞迁移变化。结果发现,Y-27632 增加了异质和同质黏附以及 E-钙黏蛋白的表达;减少了磷酸化丝切蛋白,导致 ESCC 细胞中的肌动蛋白重排。所有这些发现表明,ROCK 信号通路在细胞黏附和迁移中起着重要作用,提示它可能成为 ESCC 治疗的潜在靶点。