Literature DB >> 30942519

Crenolanib-Derived Probes Suitable for Cell- and Tissue-Based Protein Profiling and Single-Cell Imaging.

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.
© 2019 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

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


  1 in total

1.  Quantitative Proteomics Reveals Cellular Off-Targets of a DDR1 Inhibitor.

Authors:  Jiaqian Xu; Zhang Zhang; Ligen Lin; Hongyan Sun; Lorenzo V White; Ke Ding; Zhengqiu Li
Journal:  ACS Med Chem Lett       Date:  2020-02-05       Impact factor: 4.345

  1 in total

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