赫拉
细胞粘附
钙粘蛋白
化学
粘附
抗体
细胞
癌症
癌细胞
癌症研究
生物化学
生物
免疫学
有机化学
遗传学
作者
Paulina X. Medina Rangel,Elena Moroni,Franck Merlier,Levi A. Gheber,Razi Vago,Bernadette Tse Sum Bui,Karsten Haupt
标识
DOI:10.1002/anie.201910373
摘要
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.
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