癌症研究
癌细胞
癌症
弹头
肿瘤微环境
医学
病理
肿瘤细胞
生物
内科学
工程类
航空航天工程
作者
Steven Seaman,Zhongyu Zhu,Saurabh Saha,Xiaoyan M. Zhang,Mi Yang,Mary Beth Hilton,Karen Morris,Christopher Szot,Holly Morris,Deborah A. Swing,Lino Tessarollo,Sean W. Smith,Sylvia J. Degrado,Dmitry Borkin,Nareshkumar Jain,Julia Scheiermann,Yang Feng,Yanping Wang,Jinyu Li,Dean J. Welsch
出处
期刊:Cancer Cell
[Cell Press]
日期:2017-04-01
卷期号:31 (4): 501-515.e8
被引量:342
标识
DOI:10.1016/j.ccell.2017.03.005
摘要
Targeting the tumor vasculature with antibody-drug conjugates (ADCs) is a promising anti-cancer strategy that in order to be realized must overcome several obstacles, including identification of suitable targets and optimal warheads. Here, we demonstrate that the cell-surface protein CD276/B7-H3 is broadly overexpressed by multiple tumor types on both cancer cells and tumor-infiltrating blood vessels, making it a potentially ideal dual-compartment therapeutic target. In preclinical studies CD276 ADCs armed with a conventional MMAE warhead destroyed CD276-positive cancer cells, but were ineffective against tumor vasculature. In contrast, pyrrolobenzodiazepine-conjugated CD276 ADCs killed both cancer cells and tumor vasculature, eradicating large established tumors and metastases, and improving long-term overall survival. CD276-targeted dual-compartment ablation could aid in the development of highly selective broad-acting anti-cancer therapies.
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