Zhao Shi-Yi, Sun Yan, Lai Zhuo-Sheng, Nan Qing-Zhen, Li Kang, Zhang Zhen-Shu
Department of Gastroenterology, Nanfang Hospital, Southern Medical University, Guangzhou Road 1838, Guangzhou, 510515, Guangdong, China.
Mol Cell Biochem. 2009 Feb;322(1-2):179-84. doi: 10.1007/s11010-008-9955-6. Epub 2008 Nov 15.
Cell migration and invasion are triggered by a number of chemoattractants that stimulate intracellular signaling pathways through regulating reorganization of the actin cytoskeleton. Rac1, an intracellular signal transducer, regulates a variety of cell functions, including the organization of the cytoskeleton, cell migration, and invasion. However, currently, very little is known about the roles of Rac1 in the cytoskeleton formation and invasion of human colorectal cancer cells. In our study, Rac1-shRNA was used to silence the Rac1 to reduce its expression specifically in Lovo cells. Our studies showed that RNA interference-mediated deletion of Rac1 strongly inhibited lamellipodia formation, cell migration, and invasion of Lovo cells in vitro. The deletion of Rac1 can serve as an alterative therapy to inhibit the invasion and metastasis of colorectal cancer cells.
细胞迁移和侵袭由多种化学引诱剂触发,这些化学引诱剂通过调节肌动蛋白细胞骨架的重组来刺激细胞内信号通路。Rac1是一种细胞内信号转导分子,可调节多种细胞功能,包括细胞骨架的组织、细胞迁移和侵袭。然而,目前对于Rac1在人结肠癌细胞的细胞骨架形成和侵袭中的作用知之甚少。在我们的研究中,使用Rac1-shRNA使Rac1沉默,以特异性降低其在Lovo细胞中的表达。我们的研究表明,RNA干扰介导的Rac1缺失强烈抑制Lovo细胞在体外形成片状伪足、细胞迁移和侵袭。Rac1的缺失可作为一种抑制结肠癌细胞侵袭和转移的替代疗法。