The development of telomerase inhibitors: the G-quartet approach.

Anti-cancer drug design Pub Date : 1999-08-01
J L Mergny, P Mailliet, F Lavelle, J F Riou, A Laoui, C Hélène
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Abstract

Human telomeres, which consist of repeated TTAGGG sequences, have recently become the focus of intense and highly competitive biological research. This scientific interest lies in their unique biological functions: telomeres are essential for genome integrity and appear to play an important role in cellular aging and cancer. As telomerase appears to be selectively expressed in tumors versus normal cells, this enzyme represents a good target for inhibition. Different types of telomerase inhibitors have recently been described. We will present briefly the different strategies that have been proposed to achieve efficient telomerase inhibition, with a special emphasis on G-quartet ligands.

端粒酶抑制剂的发展:G-quartet方法。
人类端粒由重复的TTAGGG序列组成,近年来成为激烈而竞争激烈的生物学研究的焦点。这种科学兴趣在于它们独特的生物学功能:端粒对基因组完整性至关重要,似乎在细胞衰老和癌症中起着重要作用。由于端粒酶在肿瘤细胞和正常细胞中选择性表达,因此端粒酶是一个很好的抑制靶点。不同类型的端粒酶抑制剂最近被描述。我们将简要介绍已提出的不同策略,以实现有效的端粒酶抑制,特别强调g -四方配体。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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