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Pharmacological intervention strategies for affecting telomerase activity: Future prospects to treat cancer and degenerative disease

机译:影响端粒酶活性的药理干预策略:治疗癌症和退行性疾病的未来前景

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摘要

Telomerase enzyme is a ribonucleoprotein maintaining the length of the telomeres by adding G-rich repeats to the end of the eukaryotic chromosomes. Normal human somatic cells, cultured in vitro, have a strictly limited proliferative potential undergoing senescence after about 50-70 population doublings. In contrast, most of the tumor cells have unlimited replicative potential. Although the mechanisms of immortalization are not understood completely at a genetic level, the key role of the telomere/telomerase system in the process is clear. The DNA replication machinery is not able to replicate fully the DNA at the very end of the chromosomes; therefore, about 50-200 nucleotides are lost during each of the replication cycles resulting in a gradual decrease of telomere length. Critically short telomere induces senescence, subsequent crisis and cell death. In tumor cells, however, the telomerase enzyme prevents the formation of critically short telomeres, adding GGTTAG repeats to the 3' end of the chromosomes immortalizing the cells. Immortality is one of the hallmarks of cancer. Besides the catalytic activity dependent telomere maintenance, catalytic activity-independent effects of telomerase may also be involved in the regulation of cell cycle. The telomere/telomerase system offers two possibilities to intervene the proliferative activity of the cell: (1) inhibition the telomere maintenance by inhibiting the telomerase activity; (2) activating the residual telomerase enzyme or inducing telomerase expression. Whilst the former approach could abolish the limitless replicative potential of malignant cells, the activation of telomerase might be utilized for treating degenerative diseases.Here, we review the current status of telomerase therapeutics, summarizing the activities of those pharmacological agents which either inhibit or activate the enzyme. We also discuss the future opportunities and challenges of research on pharmacological intervention of telomerase activity.
机译:端粒酶是一种核糖核蛋白,可通过向真核染色体末端添加富含G的重复序列来维持端粒的长度。体外培养的正常人体细胞在繁殖约50-70倍后具有衰老的严格限制的增殖潜能。相反,大多数肿瘤细胞具有无限的复制潜力。尽管永生化的机制在遗传水平上尚未完全了解,但是端粒/端粒酶系统在此过程中的关键作用是清楚的。 DNA复制机制无法在染色体的最末端完全复制DNA。因此,在每个复制周期中损失约50-200个核苷酸,导致端粒长度逐渐减少。极短的端粒会引起衰老,随后的危机和细胞死亡。然而,在肿瘤细胞中,端粒酶阻止了临界短端粒的形成,在染色体的3'末端添加了GGTTAG重复序列,使细胞永生。永生是癌症的标志之一。除了催化活性依赖的端粒维持之外,端粒酶的催化活性独立作用也可能参与细胞周期的调节。端粒/端粒酶系统提供了两种干预细胞增殖活性的可能性:(1)通过抑制端粒酶活性来抑制端粒的维持; (2)激活残留的端粒酶或诱导端粒酶表达。虽然前一种方法可以消除恶性细胞的无限复制潜力,但端粒酶的激活可用于治疗退行性疾病。在此,我们回顾了端粒酶治疗的现状,总结了抑制或激活端粒酶的药理活性。酶。我们还将讨论端粒酶活性的药理干预研究的未来机遇和挑战。

著录项

  • 来源
    《Biochimie》 |2008年第1期|p.156-172|共17页
  • 作者

    I. Tarkanyi; J. Aradi;

  • 作者单位
  • 收录信息 美国《科学引文索引》(SCI);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 生物化学;
  • 关键词

  • 入库时间 2022-08-18 01:24:10

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