Oncology Research, MedImmune, LLC, Gaithersburg, Maryland.
Champions Oncology Inc., Baltimore, Maryland.
Mol Cancer Ther. 2015 Jul;14(7):1637-49. doi: 10.1158/1535-7163.MCT-14-1040. Epub 2015 May 6.
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.
ADAM17 是 HER 通路配体的主要脱落酶。我们报告了一种强效和特异的 ADAM17 抑制性抗体 MEDI3622 的发现,它在许多依赖于 EGFR 的肿瘤模型中诱导肿瘤消退或停滞。MEDI3622 的抑制活性与一系列肿瘤模型中的 EGFR 活性以及一系列聚焦的头颈部患者来源异种移植模型中的 EGFR 活性相关。在 OE21 食管模型和 COLO205 结直肠模型中,MEDI3622 的抗肿瘤活性优于 EGFR/HER 通路抑制剂,提示除了 EGFR 通路之外还有其他活性。MEDI3622 与西妥昔单抗联合应用于 OE21 模型具有相加作用,并根除了肿瘤。蛋白质组学分析揭示了新的 ADAM17 底物,这些底物在 HER 通路之外发挥作用,可能有助于单克隆抗体的抗肿瘤活性。