a Terrence Donnelly Centre for Cellular and Biomolecular Research , University of Toronto , Toronto , Canada.
b Department of Pharmaceutical Sciences, Leslie Dan Faculty of Pharmacy , University of Toronto , Toronto , Canada.
MAbs. 2018 Nov-Dec;10(8):1157-1167. doi: 10.1080/19420862.2018.1515565. Epub 2018 Sep 25.
Secreted Wnt ligands play a major role in the development and progression of many cancers by modulating signaling through cell-surface Frizzled receptors (FZDs). In order to achieve maximal effect on Wnt signaling by targeting the cell surface, we developed a synthetic antibody targeting six of the 10 human FZDs. We first identified an anti-FZD antagonist antibody (F2) with a specificity profile matching that of OMP-18R5, a monoclonal antibody that inhibits growth of many cancers by targeting FZD7, FZD1, FZD2, FZD5 and FZD8. We then used combinatorial antibody engineering by phage display to develop a variant antibody F2.A with specificity broadened to include FZD4. We confirmed that F2.A blocked binding of Wnt ligands, but not binding of Norrin, a ligand that also activates FZD4. Importantly, F2.A proved to be much more efficacious than either OMP-18R5 or F2 in inhibiting the growth of multiple RNF43-mutant pancreatic ductal adenocarcinoma cell lines, including patient-derived cells.
分泌型 Wnt 配体通过细胞表面卷曲受体(FZDs)调节信号转导,在许多癌症的发生和发展中起主要作用。为了通过靶向细胞表面来实现对 Wnt 信号的最大作用,我们开发了一种针对 10 个人类 FZDs 中的 6 个的合成抗体。我们首先鉴定了一种抗 FZD 拮抗剂抗体(F2),其特异性与 OMP-18R5 相匹配,OMP-18R5 是一种通过靶向 FZD7、FZD1、FZD2、FZD5 和 FZD8 抑制许多癌症生长的单克隆抗体。然后,我们通过噬菌体展示技术进行组合抗体工程,开发了一种变体抗体 F2.A,其特异性扩展到包括 FZD4。我们证实 F2.A 阻断了 Wnt 配体的结合,但不阻断 Norrin 的结合,Norrin 也是一种激活 FZD4 的配体。重要的是,F2.A 在抑制包括源自患者的细胞在内的多个 RNF43 突变胰腺导管腺癌细胞系的生长方面比 OMP-18R5 或 F2 更有效。