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The Solo Play of TERT Promoter Mutations

机译:TERT启动子突变的独奏

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摘要

The reactivation of telomerase reverse transcriptase (TERT) protein is the principal mechanism of telomere maintenance in cancer cells. Mutations in the promoter ( ) are a common mechanism of TERT reactivation in many solid cancers, particularly those originating from slow-replicating tissues. They are associated with increased TERT levels, telomere stabilization, and cell immortalization and proliferation. Much effort has been invested in recent years in characterizing their prevalence in different cancers and their potential as biomarkers for tumor stratification, as well as assessing their molecular mechanism of action, but much remains to be understood. Notably, they appear late in cell transformation and are mutually exclusive with each other as well as with other telomere maintenance mechanisms, indicative of overlapping selective advantages and of a strict regulation of TERT expression levels. In this review, we summarized the latest literature on the role and prevalence of mutations across different cancer types, highlighting their biased distribution. We then discussed the need to maintain TERT levels at sufficient levels to immortalize cells and promote proliferation while remaining within cell sustainability levels. A better understanding of regulation is crucial when considering its use as a possible target in antitumor strategies.
机译:端粒酶逆转录酶(TERT)蛋白的重新激活是癌细胞中端粒维持的主要机制。启动子()中的突变是许多实体癌,尤其是源自缓慢复制组织的实体癌中TERT激活的常见机制。它们与TERT水平升高,端粒稳定化以及细胞永生化和增殖有关。近年来,在描述它们在不同癌症中的流行情况以及它们作为肿瘤分层生物标志物的潜力以及评估其分子作用机理方面已经投入了很多努力,但是仍有许多工作尚待理解。值得注意的是,它们出现在细胞转化的后期,并且彼此之间以及与其他端粒维持机制互斥,表明重叠的选择性优势和对TERT表达水平的严格调节。在这篇综述中,我们总结了有关不同癌症类型中突变的作用和普遍性的最新文献,重点介绍了突变的分布。然后,我们讨论了保持足够的TERT水平以永生化细胞并促进增殖,同时保持在细胞可持续性水平内的需要。在考虑将其用作抗肿瘤策略的可能靶标时,更好地了解调控至关重要。

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