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首页> 外文期刊>Molecular cancer therapeutics >A Monoclonal Antibody to ADAM17 Inhibits Tumor Growth by Inhibiting EGFR and Non-EGFR-Mediated Pathways
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A Monoclonal Antibody to ADAM17 Inhibits Tumor Growth by Inhibiting EGFR and Non-EGFR-Mediated Pathways

机译:对Adam17的单克隆抗体通过抑制EGFR和非EGFR介导的途径来抑制肿瘤生长

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摘要

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. (C) 2015 AACR.
机译:Adam17是她的途径配体的原发性Sheddase。 我们报告了有效和特异性的AdAm17抑制抗体Medi3622的发现,其在许多Egfr依赖性肿瘤模型中诱导肿瘤回归或瘀滞。 Medi3622的抑制活性与EGFR活性在几个适应症的一系列肿瘤模型中相关,也是一组聚焦的头部和颈部患者衍生的异种移植模型。 Medi3622的抗肿瘤活性优于OE21食管模型中的EGFR / HER途径抑制剂的抑制剂和Colo205结肠直肠模型,表明EGFR途径外的附加活性。 OE21模型中Medi3622和西列昔单抗的组合是添加剂和消除的肿瘤。 蛋白质组学分析揭示了新的Adam17底物,其在途径外工作,并且可能朝着单克隆抗体的抗肿瘤活性有助于。 (c)2015年AACR。

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