A Cell-Based High-Throughput Assay for the Screening of Small-Molecule Inhibitors of p53-MDM2 Interaction

被引:13
作者
Li, Jing [1 ]
Zhang, Shuyong [1 ]
Gao, Linghuan [1 ]
Chen, Ying [1 ]
Xie, Xin [1 ]
机构
[1] Chinese Acad Sci, Shanghai Inst Mat Med, Stake Key Lab Drug Res, Natl Ctr Drug Screening, Shanghai 201203, Peoples R China
关键词
p53; MDM2; small-molecule inhibitor; protein-protein interaction; high-throughput screening; PROTEIN-PROTEIN INTERACTION; P53; FUNCTION; MDM2; ACTIVATION; TRANSACTIVATION; DATABASE; CANCER; DOMAIN; TUMORS; RITA;
D O I
10.1177/1087057111399191
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The p53 tumor suppressor is a potent transcription factor that regulates cell growth inhibition and apoptosis. The oncoprotein MDM2 suppresses p53 activity by direct inhibition of its transcriptional activity and enhances the degradation of p53 via the ubiquitin-proteosome pathway. Overexpression of MDM2, found in many human tumors, impairs p53-mediated cell death effectively. Inhibition of the p53-MDM2 interaction can stabilize p53 and may offer a novel strategy for cancer therapy. To search for new inhibitors of the p53-MDM2 interaction, the authors developed a cell-based high-throughput assay system based on mammalian two-hybrid technology. They also used a dual-luciferase reporter system to rule out false-positive hits due to the cytotoxic effect of compounds. Using this assay, they screened a library consisting of 3840 compounds and identified one compound that activates p53 pathway and induces growth arrest in tumor cells.( Journal of Biomolecular Screening. 2011; 16: 450-456)
引用
收藏
页码:450 / 456
页数:7
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