Department of Biochemistry, Dartmouth Medical School, Hanover, NH 03755, USA.
Curr Biol. 2010 Mar 23;20(6):R285-95. doi: 10.1016/j.cub.2010.01.034.
Most solid tumors are aneuploid, having a chromosome number that is not a multiple of the haploid number, and many frequently mis-segregate whole chromosomes in a phenomenon called chromosomal instability (CIN). CIN positively correlates with poor patient prognosis, indicating that reduced mitotic fidelity contributes to cancer progression by increasing genetic diversity among tumor cells. Here, we review the mechanisms underlying CIN, which include defects in chromosome cohesion, mitotic checkpoint function, centrosome copy number, kinetochore-microtubule attachment dynamics, and cell-cycle regulation. Understanding these mechanisms provides insight into the cellular consequences of CIN and reveals the possibility of exploiting CIN in cancer therapy.
大多数实体瘤是非整倍体的,其染色体数目不是单倍体数的整数倍,并且许多实体瘤经常错误地分离整个染色体,这一现象称为染色体不稳定性(CIN)。CIN 与患者预后不良呈正相关,这表明有丝分裂保真度的降低通过增加肿瘤细胞间的遗传多样性,促进了癌症的进展。在这里,我们综述了 CIN 的发生机制,包括染色体凝聚、有丝分裂检验点功能、中心体拷贝数、动粒-微管附着动力学和细胞周期调控的缺陷。了解这些机制可以深入了解 CIN 的细胞后果,并揭示了利用 CIN 进行癌症治疗的可能性。