| Literature DB >> 31659849 |
Paulina X Medina Rangel1, Elena Moroni1, Franck Merlier1, Levi A Gheber2, Razi Vago2, Bernadette Tse Sum Bui1, Karsten Haupt1.
Abstract
One of the most promising strategies to treat cancer is the use of therapeutic antibodies that disrupt cell-cell adhesion mediated by dysregulated cadherins. The principal site where cell-cell adhesion occurs encompasses Trp2 found at the N-terminal region of the protein. Herein, we employed the naturally exposed highly conserved peptide Asp1-Trp2-Val3-Ile4-Pro5-Pro6-Ile7, as epitope to prepare molecularly imprinted polymer nanoparticles (MIP-NPs) to recognize cadherins. Since MIP-NPs target the site responsible for adhesion, they were more potent than commercially available therapeutic antibodies for inhibiting cell-cell adhesion in cell aggregation assays, and for completely disrupting three-dimensional tumor spheroids as well as inhibiting invasion of HeLa cells. These biocompatible supramolecular anti-adhesives may potentially be used as immunotherapeutic or sensitizing agents to enhance antitumor effects of chemotherapy.Entities:
Keywords: adherin; cancer therapy; cell adhesion; molecularly imprinted polymer; therapeutic antibodies
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Year: 2019 PMID: 31659849 DOI: 10.1002/anie.201910373
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336