Wnt pathway inhibition via the targeting of Frizzled receptors results in decreased growth and tumorigenicity of human tumors

Austin Gurney(OncoMed (United States)), Fumiko Axelrod(OncoMed (United States)), Christopher J. Bond(OncoMed (United States)), Jennifer Cain(OncoMed (United States)), Cécile Chartier(OncoMed (United States)), Lucas Donigan(OncoMed (United States)), Marcus Fischer(OncoMed (United States)), Aurélie Chaudhari(OncoMed (United States)), May Ji(OncoMed (United States)), Ann M. Kapoun(OncoMed (United States)), Andrew Lam(OncoMed (United States)), Sasha Lazetic(OncoMed (United States)), Shirley Ma(OncoMed (United States)), Satyajit K. Mitra(OncoMed (United States)), Inkyung Park(OncoMed (United States)), Kellie Pickell(OncoMed (United States)), Aaron K. Sato(OncoMed (United States)), Sanjeev Satyal(OncoMed (United States)), Michelle Stroud(OncoMed (United States)), Hoang Tran(OncoMed (United States)), Wan-Ching Yen(OncoMed (United States)), John Lewicki(OncoMed (United States)), Timothy Hoey(OncoMed (United States))
Proceedings of the National Academy of Sciences
July 2, 2012
Cited by 624Open Access
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Abstract

The Wnt/β-catenin pathway, which signals through the Frizzled (Fzd) receptor family and several coreceptors, has long been implicated in cancer. Here we demonstrate a therapeutic approach to targeting the Wnt pathway with a monoclonal antibody, OMP-18R5. This antibody, initially identified by binding to Frizzled 7, interacts with five Fzd receptors through a conserved epitope within the extracellular domain and blocks canonical Wnt signaling induced by multiple Wnt family members. In xenograft studies with minimally passaged human tumors, this antibody inhibits the growth of a range of tumor types, reduces tumor-initiating cell frequency, and exhibits synergistic activity with standard-of-care chemotherapeutic agents.


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