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细胞周期蛋白 E 失调与基因组不稳定性。

Cyclin E Deregulation and Genomic Instability.

机构信息

Program of Cell Biology, Brazilian National Cancer Institute (INCA), Rio de Janeiro, RJ, Brazil.

Department of Cell and Molecular Biology, The Scripps Research Institute, La Jolla, CA, USA.

出版信息

Adv Exp Med Biol. 2017;1042:527-547. doi: 10.1007/978-981-10-6955-0_22.

Abstract

Precise replication of genetic material and its equal distribution to daughter cells are essential to maintain genome stability. In eukaryotes, chromosome replication and segregation are temporally uncoupled, occurring in distinct intervals of the cell cycle, S and M phases, respectively. Cyclin E accumulates at the G1/S transition, where it promotes S phase entry and progression by binding to and activating CDK2. Several lines of evidence from different models indicate that cyclin E/CDK2 deregulation causes replication stress in S phase and chromosome segregation errors in M phase, leading to genomic instability and cancer. In this chapter, we will discuss the main findings that link cyclin E/CDK2 deregulation to genomic instability and the molecular mechanisms by which cyclin E/CDK2 induces replication stress and chromosome aberrations during carcinogenesis.

摘要

精确复制遗传物质并将其均等分配到子细胞对于维持基因组稳定性至关重要。在真核生物中,染色体复制和分离在时间上是解耦的,分别发生在细胞周期的不同间隔,即 S 期和 M 期。细胞周期蛋白 E 在 G1/S 转换时积累,通过与 CDK2 结合并激活 CDK2,促进 S 期进入和进展。来自不同模型的几条证据表明,细胞周期蛋白 E/CDK2 的失调会导致 S 期的复制应激和 M 期的染色体分离错误,导致基因组不稳定和癌症。在本章中,我们将讨论将细胞周期蛋白 E/CDK2 失调与基因组不稳定性联系起来的主要发现,以及细胞周期蛋白 E/CDK2 在致癌过程中如何诱导复制应激和染色体异常的分子机制。

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