Understanding microtubule dynamics for improved cancer therapy

被引:281
作者
Honore, S [1 ]
Pasquier, E [1 ]
Braguer, D [1 ]
机构
[1] UFR Pharm, CNRS, FRE 2737, F-13005 Marseille, France
关键词
microtubule dynamics; tumor progression; microtubule-targeted drugs; mitosis; migration; cytoskeleton;
D O I
10.1007/s00018-005-5330-x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Microtubules (MTs), key components of the cytoskeleton, are dynamic polymers of tubulin that form a well-organized network of polarized tube filaments. MT dynamics are highly regulated both spacially and temporally by several MT-related proteins, themselves regulated by several kinases and phosphatases via signaling cascades, and also by coordinated interactions with actin cytoskeleton and adhesion sites. Regulation of MT dynamics is crucial for mitosis, cell migration, cell signaling and trafficking. MT-targeted drugs (MTDs), which constitute a major anticancer drug family with antimitotic and antiangiogenic properties, inhibit tumor progression mainly by altering MT dynamics in both cancer and endothelial cells. Identification of proteins regulating the MT network will lead to a better understanding of tumor progression regulators and will be helpful in improving cancer therapy.
引用
收藏
页码:3039 / 3056
页数:18
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