Origins and consequences of centrosome aberrations in human cancers

被引:169
作者
Nigg, Erich A. [1 ]
机构
[1] Max Planck Inst Biochem, Dept Cell Biol, D-82152 Martinsried, Germany
关键词
centrosome; cell cycle; chromosomal instability; aneuploidy;
D O I
10.1002/ijc.22245
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Recent years have seen a revival of interest in the possible contribution of centrosomes to the development of human cancers. The underlying hypothesis, formulated almost 100 years ago (Boveri T. The origin of malignant tumors; Baltimore, MD: Williams and Wilkins, 1929), states that numerical and/or structural centrosome abnormalities will cause me missegregation. In addition, centrosome abnormalities are expected to affect cell shape, polarity, and motility. Thus, deregulation of centrosome number and function may foster both chromosomal instability and loss of tissue architecture-2 of the most common phenotypes associated with solid human tumors. In support of the role of centrosome deregulation in tumorigenesis, centrosome aberrations have been observed in early, premalignant lesions. Moreover, they are frequent in many different types of common tumors and their prominence often correlates with poor clinical outcome. This review addresses the origins of centrosome aberrations in human tumors as well as the expected impact of centrosome aberrations on cell fate and tumor development. (c) 2006 Wiley-Liss, Inc.
引用
收藏
页码:2717 / 2723
页数:7
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