Dummler Bettina, Ohshiro Kazufumi, Kumar Rakesh, Field Jeffrey
Department of Pharmacology, University of Pennsylvania School of Medicine, Philadelphia, PA 19104, USA.
Cancer Metastasis Rev. 2009 Jun;28(1-2):51-63. doi: 10.1007/s10555-008-9168-1.
Some of the characteristics of cancer cells are high rates of cell proliferation, cell survival, and the ability to invade surrounding tissue. The cytoskeleton has an essential role in these processes. Dynamic changes in the cytoskeleton are necessary for cell motility and cancer cells are dependent on motility for invasion and metastasis. The signaling pathways behind the reshaping and migrating properties of the cytoskeleton in cancer cells involve a group of Ras-related small GTPases and their effectors, including the p21-activated kinases (Paks). Paks are a family of serine/threonine protein kinases comprised of six isoforms (Pak 1-6), all of which are direct targets of the small GTPases Rac and Cdc42. Besides their role in cytoskeletal dynamics, Paks have recently been shown to regulate various other cellular activities, including cell survival, mitosis, and transcription. Paks are overexpressed and/or hyperactivated in several human tumors and their role in cell transformation makes them attractive therapeutic targets. Pak-targeted therapeutics may efficiently inhibit certain types of tumors and efforts to identify selective Pak-inhibitors are underway.
癌细胞的一些特征是高细胞增殖率、细胞存活率以及侵袭周围组织的能力。细胞骨架在这些过程中起着至关重要的作用。细胞骨架的动态变化对于细胞运动是必要的,而癌细胞的侵袭和转移依赖于运动。癌细胞中细胞骨架重塑和迁移特性背后的信号通路涉及一组Ras相关的小GTP酶及其效应物,包括p21激活激酶(Paks)。Paks是丝氨酸/苏氨酸蛋白激酶家族,由六种亚型(Pak 1 - 6)组成,所有这些都是小GTP酶Rac和Cdc42的直接靶点。除了在细胞骨架动力学中的作用外,Paks最近还被证明可调节各种其他细胞活动,包括细胞存活、有丝分裂和转录。Paks在几种人类肿瘤中过表达和/或过度激活,它们在细胞转化中的作用使其成为有吸引力的治疗靶点。靶向Pak的疗法可能有效抑制某些类型的肿瘤,目前正在努力寻找选择性Pak抑制剂。