hIMB1636-MMAE, a Novel TROP2-Targeting Antibody-Drug Conjugate Exerting Potent Antitumor Efficacy in Pancreatic Cancer

被引:3
|
作者
Sun, Li-ping [1 ]
Bai, Wei-qi [2 ]
Zhou, Dan-dan [1 ]
Wu, Xiao-fan [2 ]
Zhang, Lan-wen [1 ]
Cui, A-long [2 ]
Xie, Zi-hui [1 ]
Gao, Rui-juan [1 ]
Zhen, Yong-su [1 ]
Li, Zhuo-Rong [2 ]
Miao, Qing-fang [1 ]
机构
[1] Chinese Acad Med Sci & Peking Union Med Coll, Inst Med Biotechnol, NHC Key Lab Biotechnol Antibiot, Beijing 100050, Peoples R China
[2] Chinese Acad Med Sci & Peking Union Med Coll, Inst Med Biotechnol, Dept Organ Chem, Beijing 100050, Peoples R China
基金
中国国家自然科学基金; 北京市自然科学基金;
关键词
SACITUZUMAB GOVITECAN IMMU-132; IN-VITRO; EXPRESSION; TARGET; TROP-2; TUMORS; PROGNOSIS; APOPTOSIS; THERAPY;
D O I
10.1021/acs.jmedchem.3c01210
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Herein, we first prepared a novel anti-TROP2 antibody-drug conjugate (ADC) hIMB1636-MMAE using hIMB1636 antibody chemically coupled to monomethyl auristatin E (MMAE) via a Valine-Citrulline linker and then reported its characteristics and antitumor activity. With a DAR of 3.92, it binds specifically to both recombinant antigen (K-D similar to 0.687 nM) and cancer cells and could be internalized by target cells and selectively kill them with IC50 values at nanomolar/subnanomolar levels by inducing apoptosis and G2/M phase arrest. hIMB1636-MMAE also inhibited cell migration, induced ADCC effects, and had bystander effects. It displayed significant tumor-targeting ability and excellent tumor-suppressive effects in vivo, resulting in 5/8 tumor elimination at 12 mg/kg in the T3M4 xenograft model or complete tumor disappearance at 10 mg/kg in BxPc-3 xenografts in nude mice. Its half-life in mice was about 87 h. These data suggested that hIMB1636-MMAE was a promising candidate for the treatment of pancreatic cancer with TROP2 overexpression.
引用
收藏
页码:14700 / 14715
页数:16
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