Progress on kinesin spindle protein inhibitors as anti-cancer agents

被引:51
|
作者
Zhang, Yingjie [1 ]
Xu, Wenfang [1 ]
机构
[1] Shandong Univ, Sch Pharmaceut Sci, Dept Med Chem, Jinan 250012, Shandong, Peoples R China
关键词
kinesin; KSP; uncompetitive inhibitor; competitive inhibitor; allosteric inhibitor;
D O I
10.2174/187152008785133119
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The kinesin spindle protein (KSP, also known as Hs Eg5) plays an essential part in the proper separation of spindle poles and the correct formation of bipolar mitotic spindle during mitosis. Inhibition of this protein results in cells apoptosis followed by mitotic arrest and the formation of characteristic monoaster spindles. Compared with the traditional chemotherapeutic agents (taxanes, vinca alkaloids), KSP inhibitors (KSPi) will not lead to the neuropathic side effects, so KSP has become a novel and an attractive anticancer target. Accordingly, more and more interest has been focused on the development of high effective and selective KSPi. This review will focus on some kinds of KSPi on the basis of introducing structure and function of KSP.
引用
收藏
页码:698 / 704
页数:7
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