Nigg Erich A
Department of Cell Biology, Max-Planck-Institute for Biochemistry, Martinsried, Germany.
Int J Cancer. 2006 Dec 15;119(12):2717-23. doi: 10.1002/ijc.22245.
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 chromosome [corrected] 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.
近年来,人们对中心体在人类癌症发展中可能发挥的作用重新产生了兴趣。近100年前提出的基本假设(博韦里T. 恶性肿瘤的起源;马里兰州巴尔的摩:威廉姆斯和威尔金斯出版社,1929年)指出,中心体的数量和/或结构异常将导致染色体[已修正]错配。此外,预计中心体异常会影响细胞形状、极性和运动性。因此,中心体数量和功能的失调可能会促进染色体不稳定和组织结构丧失——这是与人类实体瘤相关的两种最常见表型。为支持中心体失调在肿瘤发生中的作用,在早期癌前病变中已观察到中心体畸变。此外,它们在许多不同类型的常见肿瘤中很常见,并且其突出程度通常与不良临床结果相关。本综述探讨了人类肿瘤中中心体畸变的起源以及中心体畸变对细胞命运和肿瘤发展的预期影响。