In vitro and in vivo evaluation of a novel anti-EGFR antibody labeled with 89Zr and 177Lu

被引:2
|
作者
Liu, Wei [1 ,2 ]
Li, Kehong [1 ,2 ]
Deng, Hao [1 ,2 ]
Wang, Jing [2 ]
Zhao, Peng [2 ]
Liao, Wei [2 ]
Zhuo, Liangang [2 ]
Wei, Hongyuan [1 ,2 ]
Yang, Xia [2 ,3 ,4 ]
Chen, Yue [1 ]
机构
[1] Southwest Med Univ, Dept Nucl Med, Affiliated Hosp, Luzhou 646000, Peoples R China
[2] China Acad Engn Phys, Inst Nucl Phys & Chem, Mianyang 621900, Sichuan, Peoples R China
[3] Collaborat Innovat Ctr Radiat Med Jiangsu, Higher Educ Inst, Suzhou 215123, Peoples R China
[4] Key Lab Nucl Med & Mol Imaging Sichuan Prov, Mianyang 621999, Sichuan, Peoples R China
基金
中国国家自然科学基金;
关键词
EGFR; Antibody; Lung cancer; Zr-89; Lu-177; EPIDERMAL-GROWTH-FACTOR; CELL LUNG-CANCER; MONOCLONAL-ANTIBODY; RADIOIMMUNOTHERAPY; RECEPTOR; PROGNOSIS; CETUXIMAB; HEAD;
D O I
10.1007/s10967-021-08174-0
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
There is an urgent need to develop more specific targeted therapies for lung cancer treatment due to the its low survival rate. EGFR is a transmembrane tyrosine kinase protein that is overexpressed in lung cancer. Herein, a novel anti-EGFR antibody, 5A7, was modified with chelators for zirconium-89 (Zr-89) and lutetium-177 (Lu-177) labeling. The radiolabeled 5A7 could specifically bind to A549 tumor according to the in vitro and in vivo evaluation. Furthermore, the Lu-177 labeled 5A7 antibody could inhibit tumor growth significantly in A549 bearing xenografts. The radiolabeled anti-EGFR 5A7 antibody has high potential to be used for PET imaging and radiotherapy.
引用
收藏
页码:747 / 754
页数:8
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