Department of Biochemistry and Molecular Biology, Tianjin Medical University Cancer Institute and Hospital, Tianjin, China.
Cancer. 2010 Nov 15;116(22):5150-60. doi: 10.1002/cncr.25461.
The kinesin superfamily contains a conserved class of microtubule-dependent molecular motor proteins that possess an adenosine triphosphatase activity and motion characteristics. The active movement of kinesins supports several cellular functions, including mitosis, meiosis, and the transport of macromolecules. Mitosis is a process of eukaryotic cell division that involves the division of nuclei, cytoplasm, organelles, and the cell membrane into 2 daughter cells with roughly equivalent portions of these cellular components. Any errors in this process could result in cell death, abnormality (such as gene deletion, chromosome translocation, or duplication), and cancer. Because mitosis is complex and highly regulated, alteration of kinesin expression or function could lead to carcinogenesis. Moreover, because human cancer is a gene-related disease involving abnormal cell growth, targeting kinesins may create a novel strategy for the control of human cancer. Indeed, several such drugs are being tested successfully in the clinic. In this review, the authors discuss in detail the structure and function of kinesins, the correlation of kinesin expression with tumorigenesis and progression, and the development of biomarkers and cancer-targeted therapy involving the kinesin family proteins.
驱动蛋白超家族包含一组保守的微管依赖性分子马达蛋白,这些蛋白具有三磷酸腺苷酶活性和运动特性。驱动蛋白的主动运动支持多种细胞功能,包括有丝分裂、减数分裂和大分子的运输。有丝分裂是真核细胞分裂的过程,涉及细胞核、细胞质、细胞器和细胞膜分裂成 2 个子代细胞,这些细胞成分的大致相等部分。这个过程中的任何错误都可能导致细胞死亡、异常(如基因缺失、染色体易位或重复)和癌症。由于有丝分裂是复杂且高度调控的,因此驱动蛋白表达或功能的改变可能导致致癌作用。此外,由于人类癌症是一种与异常细胞生长相关的基因疾病,因此靶向驱动蛋白可能为控制人类癌症创造一种新的策略。事实上,一些这样的药物正在临床中成功地进行测试。在这篇综述中,作者详细讨论了驱动蛋白的结构和功能、驱动蛋白表达与肿瘤发生和进展的相关性,以及涉及驱动蛋白家族蛋白的生物标志物和癌症靶向治疗的发展。