Microtubule inhibitors: Differentiating tubulin-inhibiting agents based on mechanisms of action, clinical activity, and resistance

被引:427
作者
Perez, Edith A. [1 ]
机构
[1] Mayo Clin, Div Hematol & Oncol, Jacksonville, FL 32224 USA
关键词
P-GLYCOPROTEIN INHIBITOR; ERIBULIN MESYLATE E7389; ADVANCED BREAST-CANCER; HALICHONDRIN-B ANALOG; III BETA-TUBULIN; PHASE-II; EPOTHILONE-B; IXABEPILONE BMS-247550; VINCA ALKALOIDS; PACLITAXEL RESISTANCE;
D O I
10.1158/1535-7163.MCT-09-0366
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Microtubules are important cellular targets for anticancer therapy because of their key role in mitosis. Microtubule inhibitors (MTI) such as taxanes, vinca alkaloids, and epothilones stabilize or destabilize microtubules, thereby suppressing microtubule dynamics required for proper mitotic function, effectively blocking cell cycle progression and resulting in apoptosis. In spite of their antitumor activity, innate or acquired drug resistance to MTIs such as the taxanes is common, limiting their overall clinical efficacy. Further insight into the mechanisms of action of microtubule-targeting drugs has lead to the discovery of novel agents that may provide higher efficacy with limited toxicity and help overcome resistance to conventional MTIs. This review will focus on the different mechanisms of action of MTIs, potential factors related to resistance and tolerability, and will discuss the recent approval as well as the development of new antineoplastic agents. [Mol Cancer Ther 2009;8(8):2086-95]
引用
收藏
页码:2086 / 2095
页数:10
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