Ghosh Science and Technology Center, Department of Biology, Worcester State University, Worcester, MA, USA.
Anticancer Res. 2011 Nov;31(11):3645-57.
Rho kinase (ROCK) proteins are Rho-GTPase activated serine/threonine kinases that function as modulators of actin-myosin cytoskeletal dynamics via regulation of Lin11, Isl-1 & Mec-3 domain (LIM) kinase, myosin light chain (MLC), and MLC phosphatase. A strong correlation between cytoskeletal rearrangements and tumor cell invasion, metastasis, and deregulated microenvironment interaction has been reported in the literature, and the utilization of pharmacological inhibitors of ROCK signaling for the treatment of cancer is actively being pursued by a number of pharmaceutical companies. Indeed, in many preclinical models ROCK inhibitors have shown remarkable efficacy in reducing tumor growth and metastasis. Interestingly, ROCK signaling has been shown to be either pro-apoptotic or pro-survival in a cell type and context dependent manner, though the molecular mechanisms controlling ROCK-mediated cell fate decisions are unknown. This review summarizes the many pleiotropic roles of ROCK signaling in survival and apoptosis, and suggests that controlled modulation of ROCK activity in tumor cells has the potential to significantly affect tumor survival and patient outcome.
Rho 激酶(ROCK)蛋白是 Rho-GTP 酶激活的丝氨酸/苏氨酸激酶,通过调节 Lin11、Isl-1 和 Mec-3 结构域(LIM)激酶、肌球蛋白轻链(MLC)和 MLC 磷酸酶,作为肌动球蛋白细胞骨架动力学的调节剂发挥作用。文献中报道了细胞骨架重排与肿瘤细胞侵袭、转移和失调的微环境相互作用之间的强烈相关性,许多制药公司正在积极利用 ROCK 信号转导的药理学抑制剂来治疗癌症。事实上,在许多临床前模型中,ROCK 抑制剂在减少肿瘤生长和转移方面显示出显著的疗效。有趣的是,ROCK 信号转导以细胞类型和上下文依赖的方式表现为促凋亡或抗凋亡,尽管控制 ROCK 介导的细胞命运决定的分子机制尚不清楚。本综述总结了 ROCK 信号转导在存活和凋亡中的许多多效作用,并表明肿瘤细胞中 ROCK 活性的受控调节有可能显著影响肿瘤的存活和患者的预后。