| Literature DB >> 30183492 |
Zvezdan Pavlovic1, Jarrett J Adams1, Levi L Blazer1, Amandeep K Gakhal1, Nick Jarvik1, Zachary Steinhart2, Mélanie Robitaille2, Keith Mascall2, James Pan1, Stephane Angers2,3, Jason Moffat1,4,5, Sachdev S Sidhu1,4.
Abstract
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.Entities:
Keywords: Wnt signaling; anti-Frizzled synthetic antibodies; pancreatic ductal adenocarcinoma; phage display
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Year: 2018 PMID: 30183492 PMCID: PMC6284576 DOI: 10.1080/19420862.2018.1515565
Source DB: PubMed Journal: MAbs ISSN: 1942-0862 Impact factor: 5.857