Mario Niepel, Marc Hafner, Mirra Chung, Peter K. Sorger
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引用次数: 32
Abstract
Measuring the potencies of small-molecule drugs in cell lines is a critical aspect of preclinical pharmacology. Such experiments are also prototypical of high-throughput experiments in multi-well plates. The procedure is simple in principle, but many unrecognized factors can affect the results, potentially making data unreliable. The procedures for measuring drug response described here were developed by the NIH LINCS program to improve reproducibility. Key features include maximizing uniform cell growth during the assay period, accounting for the effects of cell density on response, and correcting sensitivity measures for differences in proliferation rates. Two related protocols are described: one involves an endpoint measure well-suited to large-scale studies and the second is a time-dependent measurement that reveals changes in response over time. The methods can be adapted to other types of plate-based experiments. © 2017 by John Wiley & Sons, Inc.
肿瘤培养细胞的药物敏感性和耐药性测定
在细胞系中测量小分子药物的效力是临床前药理学的一个重要方面。这种实验也是多孔板高通量实验的典型。该过程原则上很简单,但许多未被认识到的因素会影响结果,可能使数据不可靠。本文描述的药物反应测量程序是由NIH LINCS项目开发的,以提高可重复性。主要特点包括在测定期间最大限度地均匀细胞生长,考虑细胞密度对反应的影响,以及校正增殖率差异的敏感性措施。描述了两种相关的方案:一种涉及非常适合大规模研究的终点测量,另一种是随时间变化的测量,揭示了反应随时间的变化。该方法可适用于其他类型的平板实验。©2017 by John Wiley &儿子,Inc。
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