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首页> 外文期刊>Journal of biomedical science. >Mechanisms of human telomerase reverse transcriptase (hEmphasis Type="Italic"TERT/Emphasis) regulation: clinical impacts in cancer
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Mechanisms of human telomerase reverse transcriptase (hEmphasis Type="Italic"TERT/Emphasis) regulation: clinical impacts in cancer

机译:人类端粒酶逆转录酶(h TERT )调节的机制:对癌症的临床影响

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BackgroundLimitless self-renewal is one of the hallmarks of cancer and is attained by telomere maintenance, essentially through telomerase (h TERT ) activation. Transcriptional regulation of h TERT is believed to play a major role in telomerase activation in human cancers.Main bodyThe dominant interest in telomerase results from its role in cancer. The role of telomeres and telomere maintenance mechanisms is well established as a major driving force in generating chromosomal and genomic instability. Cancer cells have acquired the ability to overcome their fate of senescence via telomere length maintenance mechanisms, mainly by telomerase activation.h TERT expression is up-regulated in tumors via multiple genetic and epigenetic mechanisms including h TERT amplifications, h TERT structural variants, h TERT promoter mutations and epigenetic modifications through h TERT promoter methylation. Genetic (h TERT promoter mutations) and epigenetic (h TERT promoter methylation and miRNAs) events were shown to have clinical implications in cancers that depend on h TERT activation. Knowing that telomeres are crucial for cellular self-renewal, the mechanisms responsible for telomere maintenance have a crucial role in cancer diseases and might be important oncological biomarkers. Thus, rather than quantifying TERT expression and its correlation with telomerase activation, the discovery and the assessment of the mechanisms responsible for TERT upregulation offers important information that may be used for diagnosis, prognosis, and treatment monitoring in oncology. Furthermore, a better understanding of these mechanisms may promote their translation into effective targeted cancer therapies.ConclusionHerein, we reviewed the underlying mechanisms of h TERT regulation, their role in oncogenesis, and the potential clinical applications in telomerase-dependent cancers.
机译:背景无限的自我更新是癌症的标志之一,并且通过端粒的维持(主要是通过端粒酶(h TERT)激活)来实现。人们认为h TERT的转录调控在端粒酶激活人类癌症中起主要作用。主体端粒酶的主要兴趣来自其在癌症中的作用。端粒和端粒维持机制的作用已被很好地确立为产生染色体和基因组不稳定性的主要驱动力。癌细胞已具有通过端粒长度维持机制(主要是通过端粒酶激活)克服衰老命运的能力。h TERT表达通过多种遗传和表观遗传机制(包括h TERT扩增,h TERT结构变异,h TERT)在肿瘤中上调。启动子突变和通过h TERT启动子甲基化的表观遗传修饰。遗传(h TERT启动子突变)和表观遗传(h TERT启动子甲基化和miRNA)事件在依赖h TERT激活的癌症中具有临床意义。知道端粒对于细胞自我更新至关重要,负责端粒维持的机制在癌症疾病中具有至关重要的作用,并且可能是重要的肿瘤生物标志物。因此,与其量化TERT的表达及其与端粒酶激活的相关性,不如对TERT上调负责的机制的发现和评估提供重要的信息,这些信息可用于肿瘤学的诊断,预后和治疗监测。此外,对这些机制的更好的理解可能会促进其转化为有效的靶向癌症治疗。

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