An anti-TROP2 monoclonal antibody TrMab-6 exerts antitumor activity in breast cancer mouse xenograft models

被引:14
作者
Tanaka, Tomohiro [1 ]
Ohishi, Tomokazu [2 ]
Asano, Teizo [1 ]
Takei, Junko [1 ,3 ]
Nanamiya, Ren [1 ]
Hosono, Hideki [1 ]
Sano, Masato [1 ]
Harada, Hiroyuki [3 ]
Kawada, Manabu [2 ]
Kaneko, Mika K. [1 ]
Kato, Yukinari [1 ,4 ]
机构
[1] Tohoku Univ, Dept Antibody Drug Dev, Grad Sch Med, Aoba Ku, Sendai, Miyagi 9808575, Japan
[2] Microbial Chem Res Fdn, Inst Microbial Chem BIKAKEN, Numazu, Shizuoka 4100301, Japan
[3] Tokyo Med & Dent Univ, Grad Sch Med & Dent Sci, Dept Oral & Maxillofacial Surg, Bunkyo Ku, Tokyo 1138510, Japan
[4] Tohoku Univ, New Ind Creat Hatchery Ctr, Aoba Ku, 2-1 Seiryo Machi, Sendai, Miyagi 9808575, Japan
基金
日本学术振兴会;
关键词
TROP2; monoclonal antibody; ADCC; CDC; antitumor activity; breast cancer; SOLID TUMORS; TROP2; OVEREXPRESSION; EXPRESSION; EPCAM; PROGNOSIS; INVASION; IMPACT; COULD;
D O I
10.3892/or.2021.8083
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Trophoblast cell surface antigen 2 (TROP2), reported to be overexpressed in several types of cancer, is involved in cell proliferation, invasion, metastasis, and poor prognosis of many types of cancer. Previously, a highly sensitive anti-TROP2 monoclonal antibody (clone TrMab-6; mouse IgG(2b), kappa) was developed using a Cell-Based Immunization and Screening (CBIS) method. TrMab-6 was useful for investigations using flow cytometry, western blot, and immunohistochemistry. The aim of the present study was to investigate whether TrMab-6 possesses in vitro antibody-dependent cellular cytotoxicity (ADCC) or complement-dependent cytotoxicity (CDC) activities or in vivo antitumor activities using mouse xenograft models of TROP2-overexpressed CHO-K1 (CHO/TROP2) and breast cancer cell lines, including MCF7, MDA-MB-231, and MDA-MB-468. In vitro experiments revealed that TrMab-6 strongly induced ADCC and CDC activities against CHO/TROP2 and the three breast cancer cell lines, whereas it did not show those activities against parental CHO-K1 and MCF7/TROP2-knockout cells. Furthermore, in vivo experiments on CHO/TROP2 and MCF7 xenografts revealed that TrMab-6 significantly reduced tumor growth, whereas it did not show antitumor activities against parental CHO-K1 and MCF7/TROP2-knockout xenografts. The findings suggest that TrMab-6 is a promising treatment option for TROP2-expressing breast cancers.
引用
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页数:10
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