An Image-Based, High-Throughput Screening Assay for Molecules that Induce Excess DNA Replication in Human Cancer Cells

被引:17
|
作者
Zhu, Wenge [1 ]
Lee, Chrissie Y. [1 ]
Johnson, Ronald L. [2 ]
Wichterman, Jennifer [2 ]
Huang, Ruili [2 ]
DePamphilis, Melvin L. [1 ]
机构
[1] NICHHD, NIH, Bethesda, MD 20892 USA
[2] NIH, NIH Chem Genom Ctr, Rockville, MD USA
关键词
PROTEIN-KINASE INHIBITORS; CDT1-GEMININ INTERACTION; IN-VITRO; TUBULIN POLYMERIZATION; BIOLOGICAL-ACTIVITIES; ANTIALCOHOLISM DRUG; PROTEASOME ACTIVITY; MITOTIC SLIPPAGE; BREAST-CANCER; BONE-MARROW;
D O I
10.1158/1541-7786.MCR-10-0570
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Previous studies have shown DNA re-replication can be induced in cells derived from human cancers under conditions in which it is not possible for cells derived from normal tissues. Because DNA re-replication induces cell death, this strategy could be applied to the discovery of potential anticancer therapeutics. Therefore, an imaging assay amenable to high-throughput screening was developed that measures DNA replication in excess of four genomic equivalents in the nuclei of intact cells and indexes cell proliferation. This assay was validated by screening a library of 1,280 bioactive molecules on both normal and tumor-derived cells where it proved more sensitive than current methods for detecting excess DNA replication. This screen identified known inducers of excess DNA replication, such as inhibitors of microtubule dynamics, and novel compounds that induced excess DNA replication in both normal and cancer cells. In addition, two compounds were identified that induced excess DNA replication selectively in cancer cells and one that induced endocycles selectively in cancer cells. Thus, this assay provides a new approach to the discovery of compounds useful for investigating the regulation of genome duplication and for the treatment of cancer. Mol Cancer Res; 9(3); 294-310. (C) 2011 AACR.
引用
收藏
页码:294 / 310
页数:17
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