Reactivation of telomerase in cancer.

Semih Can Akincilar, Bilal Unal, Vinay Tergaonkar
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Abstract

Activation of telomerase is a critical step in the development of about 85 % of human cancers. Levels of Tert, which encodes the reverse transcriptase subunit of telomerase, are limiting in normal somatic cells. Tert is subjected to transcriptional, post-transcriptional and epigenetic regulation, but the precise mechanism of how telomerase is re-activated in cancer cells is poorly understood. Reactivation of the Tert promoter involves multiple changes which evolve during cancer progression including mutations and chromosomal re-arrangements. Newly described non-coding mutations in the Tert promoter region of many cancer cells (19 %) in two key positions, C250T and C228T, have added another layer of complexity to telomerase reactivation. These mutations create novel consensus sequences for transcription factors which can enhance Tert expression. In this review, we will discuss gene structure and function of Tert and provide insights into the mechanisms of Tert reactivation in cancers, highlighting the contribution of recently identified Tert promoter mutations.

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癌症中端粒酶的重新激活。
端粒酶的激活是约 85% 的人类癌症发生的关键步骤。在正常体细胞中,编码端粒酶反转录酶亚基的Tert的水平是有限的。Tert受到转录、转录后和表观遗传学的调控,但人们对端粒酶如何在癌细胞中重新激活的确切机制却知之甚少。Tert 启动子的重新激活涉及癌症发展过程中的多种变化,包括突变和染色体重新排列。在许多癌细胞(19%)的 Tert 启动子区域的两个关键位置,即 C250T 和 C228T,新发现的非编码突变增加了端粒酶再激活的复杂性。这些突变为转录因子创造了新的共识序列,可以增强 Tert 的表达。在这篇综述中,我们将讨论Tert的基因结构和功能,并深入探讨癌症中Tert再激活的机制,重点介绍最近发现的Tert启动子突变的贡献。
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