| Literature DB >> 25948294 |
Jonathan Rios-Doria1, Darrin Sabol1, Jon Chesebrough1, Dave Stewart1, Linda Xu1, Ravinder Tammali1, Li Cheng1, Qun Du1, Kevin Schifferli1, Ray Rothstein1, Ching Ching Leow1, Jenny Heidbrink-Thompson1, Xiaofang Jin1, Changshou Gao1, Jay Friedman2, Brandy Wilkinson2, Melissa Damschroder1, Andrew J Pierce1, Robert E Hollingsworth1, David A Tice1, Emil F Michelotti3.
Abstract
ADAM17 is the primary sheddase for HER pathway ligands. We report the discovery of a potent and specific ADAM17 inhibitory antibody, MEDI3622, which induces tumor regression or stasis in many EGFR-dependent tumor models. The inhibitory activity of MEDI3622 correlated with EGFR activity both in a series of tumor models across several indications as well in as a focused set of head and neck patient-derived xenograft models. The antitumor activity of MEDI3622 was superior to that of EGFR/HER pathway inhibitors in the OE21 esophageal model and the COLO205 colorectal model suggesting additional activity outside of the EGFR pathway. Combination of MEDI3622 and cetuximab in the OE21 model was additive and eradicated tumors. Proteomics analysis revealed novel ADAM17 substrates that function outside of the HER pathways and may contribute toward the antitumor activity of the monoclonal antibody. ©2015 American Association for Cancer Research.Entities:
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Year: 2015 PMID: 25948294 DOI: 10.1158/1535-7163.MCT-14-1040
Source DB: PubMed Journal: Mol Cancer Ther ISSN: 1535-7163 Impact factor: 6.261