| Literature DB >> 30942519 |
Yu Chang1, Dongsheng Zhu2,3, Haijun Guo1, Xingfeng Yin4, Ke Ding1, Zhengqiu Li1.
Abstract
Crenolanib (CP-868,596), a potent inhibitor of FLT3 and PDGFRα/β, is currently under phase III clinical investigation for the treatment of acute myeloid leukemia. However, the protein targets of Crenolanib in cancer cells remain obscure, which results in difficulties in understanding the mechanism of actions and side effects. To alleviate this issue, in this study, a photoaffinity probe and two fluorescent probes were created based on Crenolanib, followed by competitive protein profiling and bioimaging studies, with the aim of characterizing the cellular targets. A series of unknown protein hits, such as MAPK1, SHMT2, SLC25A11, and HIGD1A, were successfully identified by means of pull-down/LC-MS/MS; these might provide valuable clues for understanding drug action and potential toxicities. Moreover, the fluorescent probes are suitable for imaging drug distribution at the single-cell level.Entities:
Keywords: cancer; fluorescence; imaging agents; inhibitors; proteomics
Year: 2019 PMID: 30942519 DOI: 10.1002/cbic.201900067
Source DB: PubMed Journal: Chembiochem ISSN: 1439-4227 Impact factor: 3.164