多种机制有助于端粒维护。

Journal of cancer biology & research Pub Date : 2013-11-19
Tammy A Morrish, Dulat Bekbolysnov, David Velliquette, Michelle Morgan, Bryan Ross, Yongheng Wang, Benjamin Chaney, Jessica McQuigg, Nathan Fager, Ira P Maine
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引用次数: 0

摘要

肿瘤的无限生长潜力取决于端粒的维持,通常取决于端粒酶,一种依赖RNA的DNA聚合酶,它逆转录端粒酶RNA模板,在染色体末端合成端粒重复序列。对端粒酶基因缺失的多种模式生物的研究表明,一些基于重组的机制也有助于端粒的维持。了解这些机制的分子基础是至关重要的,因为一些人类肿瘤的形成没有端粒酶,但序列在端粒中维持。在表达端粒酶的肿瘤中,基于重组的机制也可能在一定频率上促进端粒的维持。预防端粒维持预计会影响肿瘤生长,而抑制端粒酶可能选择基于重组的机制。端粒重组机制可能涉及DNA修复途径的改变或不受调节。一些DNA损伤剂的使用可能会鼓励利用这些不受管制的DNA修复途径,并可能允许一些肿瘤对这些药物产生耐药性,这取决于肿瘤中哪些修复途径发生了改变。这篇综述将讨论各种端粒重组机制,并将提供关于L1反转录转位可能有助于端粒缺乏肿瘤的端粒维持的可能性的基本原理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Multiple Mechanisms Contribute To Telomere Maintenance.

The unlimited growth potential of tumors depends on telomere maintenance and typically depends on telomerase, an RNA-dependent DNA polymerase, which reverse transcribes the telomerase RNA template, synthesizing telomere repeats at the ends of chromosomes. Studies in various model organisms genetically deleted for telomerase indicate that several recombination-based mechanisms also contribute to telomere maintenance. Understanding the molecular basis of these mechanisms is critical since some human tumors form without telomerase, yet the sequence is maintained at the telomeres. Recombination-based mechanisms also likely contribute at some frequency to telomere maintenance in tumors expressing telomerase. Preventing telomere maintenance is predicted to impact tumor growth, yet inhibiting telomerase may select for the recombination-based mechanisms. Telomere recombination mechanisms likely involve altered or unregulated pathways of DNA repair. The use of some DNA damaging agents may encourage the use of these unregulated pathways of DNA repair to be utilized and may allow some tumors to generate resistance to these agents depending on which repair pathways are altered in the tumors. This review will discuss the various telomere recombination mechanisms and will provide rationale regarding the possibility that L1 retrotransposition may contribute to telomere maintenance in tumors lacking telomerase.

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