Gunaratnam Mekala, Neidle Stephen
The Cancer Research UK Biomolecular Structure Group, The School of Pharmacy, University of London, London, UK.
Methods Mol Biol. 2010;613:303-13. doi: 10.1007/978-1-60327-418-0_19.
The targeting of telomerase and telomere maintenance in human cancer cells can be achieved by small molecules that induce the 3'single-stranded ends of telomeric DNA to fold up into four-stranded quadruplex structures that inhibit the action of the telomerase enzyme complex. In this chapter, we describe a series of biochemical, biophysical, and cellular assays that are used to evaluate the activity of new compounds, and so assess whether they are suitable for examination in xenograft models of human cancer. These assays evaluate quadruplex stabilisation properties, short- and long-term cell viability, telomerase enzymatic activity, cellular senescence, and telomere length changes.
通过小分子可实现对人类癌细胞中端粒酶和端粒维持的靶向作用,这些小分子能诱导端粒DNA的3'单链末端折叠成四链体结构,从而抑制端粒酶复合物的作用。在本章中,我们描述了一系列生化、生物物理和细胞分析方法,用于评估新化合物的活性,进而判断它们是否适合在人类癌症异种移植模型中进行检测。这些分析方法可评估四链体稳定特性、短期和长期细胞活力、端粒酶活性、细胞衰老以及端粒长度变化。