| Literature DB >> 28920432 |
Ji-Ting Hou1, Kyung-Phil Ko, Hu Shi2, Wen Xiu Ren, Peter Verwilst, Seyoung Koo, Jin Yong Lee2, Sung-Gil Chi, Jong Seung Kim.
Abstract
As significantly expressed during cell division, polo-like kinase 1 (PLK1) plays crucial roles in numerous mitotic events and has attracted interest as a potential therapeutic marker in oncological drug discovery. We prepared two small molecular fluorescent probes, 1 and 2, conjugated to SBE13 (a type II PLK1 inhibitor) to investigate the PLK1-targeted imaging of cancer cells and tumors. Enzymatic docking studies, molecular dynamics simulations, and in vitro and in vivo imaging experiments all supported the selective targeting and visualization of PLK1 expressing cells by probes 1 and 2, and probe 2 was successfully demonstrated to image PLK1-upregulated tumors with remarkable signal-to-background ratios. These findings represent the first example of small-molecule based fluorescent imaging of tumors using PLK1 as a target, which could provide new avenues for tumor diagnosis and precision therapeutics.Entities:
Keywords: PLK1; SBE13; fluorescence; high SBR ratio; targeted imaging
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Year: 2017 PMID: 28920432 DOI: 10.1021/acssensors.7b00544
Source DB: PubMed Journal: ACS Sens ISSN: 2379-3694 Impact factor: 7.711