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MicroRNA Regulation of Telomerase Reverse Transcriptase (TERT): Micro Machines Pull Strings of Papier-Mâché Puppets

机译:端粒酶逆转录酶(TERT)的MicroRNA调节:微型机器拉纸的Papier-Mâché木偶的字符串

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摘要

Substantial fraction of high-quality information is continuously being added into the existing pool of knowledge related to the biology of telomeres. Based on the insights gleaned from decades of research, it is clear that chromosomal stability needs a highly controlled and dynamic balance of DNA gain and loss in each terminal tract of telomeric repeats. Telomeres are formed by tandem repeats of TTAGGG sequences, which are gradually lost with each round of division of the cells. Targeted inhibition of telomerase to effectively induce apoptosis in cancer cells has attracted tremendous attention and overwhelmingly increasingly list of telomerase inhibitors truthfully advocates pharmacological significance of telomerase. Telomerase reverse transcriptase (TERT) is a multi-talented and catalytically active component of the telomerase-associated protein machinery. Different proteins of telomerase-associated machinery work in a synchronized and orchestrated manner to ensure proper maintenance of telomeric length of chromosomes. Rapidly emerging scientific findings about regulation of TERT by microRNAs has revolutionized our understanding related to the biology of telomeres and telomerase. In this review, we have comprehensively discussed how different miRNAs regulate TERT in different cancers. Use of miRNA-based therapeutics against TERT in different cancers needs detailed research in preclinical models for effective translation of laboratory findings to clinically effective therapeutics.
机译:大量高质量的信息不断被添加到与端粒生物学相关的现有知识库中。根据数十年来研究的见解,很明显,染色体稳定性需要端粒重复序列每个末端区域中DNA得失的高度受控和动态平衡。端粒由TTAGGG序列的串联重复序列形成,随着细胞分裂的每一轮逐渐消失。靶向抑制端粒酶以有效诱导癌细胞凋亡引起了极大的关注,并且端粒酶抑制剂的泛滥越来越多地真实地提倡端粒酶的药理学意义。端粒酶逆转录酶(TERT)是端粒酶相关蛋白机制的一种多才多艺且具有催化活性的成分。端粒酶相关机制的不同蛋白质以同步和精心安排的方式工作,以确保正确维持染色体的端粒长度。关于microRNA调控TERT的迅速出现的科学发现,彻底改变了我们对端粒和端粒酶生物学的认识。在这篇综述中,我们已经全面讨论了不同的miRNA如何调节不同癌症中的TERT。基于miRNA的针对TERT的疗法在不同癌症中的使用需要在临床前模型中进行详细研究,以将实验室发现有效转化为临床有效疗法。

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