Targeting the Kinesin Spindle Protein: Basic Principles and Clinical Implications

被引:128
作者
Sarli, Vasiliki [1 ]
Giannis, Athanassios [1 ]
机构
[1] Univ Leipzig, Inst Organ Chem, D-04103 Leipzig, Germany
关键词
D O I
10.1158/1078-0432.CCR-08-0120
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Kinesin spindle protein (KSP), a member of the kinesin superfamily of microtubule-based motors, plays a critical role in mitosis as it mediates centrosome separation and bipolar spindle assembly and maintenance. Inhibition of KSP function leads to cell cycle arrest at mitosis with the formation of monoastral microtubule arrays, and ultimately, to cell death. Several KSP inhibitors are currently being studied in clinical trials and provide new opportunities for the development of novel anticancer therapeutics alternative from the available microtubule targeting drugs.
引用
收藏
页码:7583 / 7587
页数:5
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