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端粒缺失作为人类癌症中染色体不稳定性的机制。

Telomere loss as a mechanism for chromosome instability in human cancer.

机构信息

Department of Radiation Oncology, University of California San Francisco, San Francisco, CA 94143-1331, USA.

出版信息

Cancer Res. 2010 Jun 1;70(11):4255-9. doi: 10.1158/0008-5472.CAN-09-4357. Epub 2010 May 18.

Abstract

Cancer cells commonly have a high rate of telomere loss, even when expressing telomerase, contributing to chromosome instability and tumor cell progression. This review addresses the hypothesis that this high rate of telomere loss results from a combination of four factors. The first factor is an increase in the frequency of double-strand breaks (DSB) at fragile sites in cancer cells due to replication stress. The second factor is that telomeres are fragile sites. The third factor is that subtelomeric regions are highly sensitive to DSBs, so that DSBs near telomeres have an increased probability of resulting in chromosome instability. The fourth factor is that cancer cells may be deficient in chromosome healing, the de novo addition of telomeres to the sites of DSBs, a mechanism that prevents chromosome instability resulting from DSBs near telomeres. Understanding these factors and how they influence telomere loss will provide important insights into the mechanisms of chromosome instability and the development of novel approaches for anti-cancer therapy. Cancer Res; 70(11); 4255-9. (c)2010 AACR.

摘要

癌细胞通常具有较高的端粒丢失率,即使表达端粒酶也是如此,这导致了染色体不稳定和肿瘤细胞的进展。本综述探讨了这样一种假设,即这种高的端粒丢失率是由四个因素共同作用的结果。第一个因素是由于复制应激,在癌细胞中的脆性部位双链断裂(DSB)的频率增加。第二个因素是端粒是脆性部位。第三个因素是端粒附近的亚端粒区域对 DSB 非常敏感,因此端粒附近的 DSB 更有可能导致染色体不稳定。第四个因素是癌细胞可能缺乏染色体修复,即端粒酶在 DSB 部位的从头添加,这一机制可以防止端粒附近的 DSB 导致染色体不稳定。了解这些因素以及它们如何影响端粒丢失将为染色体不稳定性的机制和抗癌治疗新方法的开发提供重要的见解。癌症研究;70(11);4255-9。(c)2010AACR。

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