A Robust High-Content Imaging Approach for Probing the Mechanism of Action and Phenotypic Outcomes of Cell-Cycle Modulators

被引:22
|
作者
Sutherland, Jeffrey J. [1 ]
Low, Jonathan [2 ]
Blosser, Wayne [2 ]
Dowless, Michele [2 ]
Engler, Thomas A. [3 ]
Stancato, Louis F. [2 ]
机构
[1] Eli Lilly & Co, Lilly Corp Ctr, Lilly Res Labs Informat Technol, Indianapolis, IN 46285 USA
[2] Eli Lilly & Co, Canc Biol & Patient Tailoring, Indianapolis, IN 46285 USA
[3] Eli Lilly & Co, Discovery Chem Res & Technol, Indianapolis, IN 46285 USA
关键词
SMALL-MOLECULE INHIBITOR; IN-VITRO; DEPENDENT KINASES; CENTROMERE DYNAMICS; ANTICANCER DRUGS; TOPOISOMERASE-I; AURORA KINASES; POLO; VIVO; TARGET;
D O I
10.1158/1535-7163.MCT-10-0720
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
High-content screening is increasingly used to elucidate changes in cellular biology arising from treatment with small molecules and biological probes. We describe a cell classifier for automated analysis of multiparametric data from immunofluorescence microscopy and characterize the phenotypes of 41 cell-cycle modulators, including several protein kinase inhibitors in preclinical and clinical development. This method produces a consistent assessment of treatment-induced phenotypes across experiments done by different biologists and highlights the prevalence of nonuniform and concentration-dependent cellular response to treatment. Contrasting cell phenotypes from high-content screening to kinase selectivity profiles from cell-free assays highlights the limited utility of enzyme potency ratios in understanding the mechanism of action for cell-cycle kinase inhibitors. Our cell-level approach for assessing phenotypic outcomes is reliable, reproducible and capable of supporting medium throughput analyses of a wide range of cellular perturbations. Mol Cancer Ther; 10(2); 242-54. (C)2011 AACR.
引用
收藏
页码:242 / 254
页数:13
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