| Literature DB >> 32052897 |
Pai Liu1,2, Weiqiang Fu1, Peter Verwilst2,3, Miae Won2, Jinwoo Shin2, Zhengxu Cai1, Bin Tong1, Jianbing Shi1, Yuping Dong1, Jong Seung Kim2.
Abstract
Heteroatom-containing spiropolymers were constructed in a facile manner by a catalyst-free multicomponent spiropolymerization route. P1a2b as the most potent of these spiropolymers, demonstrates cluster-triggered emission resulting from strong interactions with the MDM2 protein. By preventing the anti-apoptotic p53/MDM2 interaction, P1a2b triggers apoptosis in cancerous cells, while demonstrating a good biocompatibility and non-toxicity in non-cancerous cells. The combined results from solution and cell-based cluster-triggered emission studies, docking, protein expression experiments and cytotoxicity data strongly support the MDM2-binding hypothesis and indicate a potential application as a fluorescent cancer marker as well as therapeutic for this spiropolymer.Entities:
Keywords: MDM2 inhibitor; cell apoptosis; clusterization-triggered emission; spiropolymerization; theranostics
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Year: 2020 PMID: 32052897 DOI: 10.1002/anie.201916524
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336