H2Mab-19, an anti-human epidermal growth factor receptor 2 monoclonal antibody exerts antitumor activity in mouse oral cancer xenografts

被引:15
作者
Takei, Junko [1 ,2 ]
Kaneko, Mika Kato [1 ]
Ohishi, Tomokazu [3 ]
Kawada, Manabu [3 ]
Harada, Hiroyuki [2 ]
Kato, Yukinari [1 ,4 ]
机构
[1] Tohoku Univ, Dept Antibody Drug Dev, Grad Sch Med, Sendai, Miyagi 9808575, Japan
[2] Tokyo Med & Dent Univ, Grad Sch Med & Dent Sci, Dept Oral & Maxillofacial Surg, Tokyo 1138510, Japan
[3] Microbial Chem Res Fdn, Inst Microbial Chem BIKAKEN, Numazu, Shizuoka 4100301, Japan
[4] Tohoku Univ, New Ind Creat Hatchery Ctr, Sendai, Miyagi 9808575, Japan
基金
日本学术振兴会;
关键词
HSC-2; monoclonal antibody; antitumor activity; SQUAMOUS-CELL CARCINOMA; METASTATIC BREAST-CANCER; DRUG CONJUGATE; CHEMOTHERAPY PLUS; HUMAN PODOPLANIN; HER2; EXPRESSION; TRASTUZUMAB; HEAD; SURVIVAL; AMPLIFICATION;
D O I
10.3892/etm.2020.8765
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Human epidermal growth factor receptor 2 (HER2) is reported to be overexpressed in breast cancers and is associated with poor clinical outcome. Trastuzumab is a humanized anti-HER2 antibody that offers significant survival benefits to patients with HER2-overexpressing breast cancer. In this study, a novel anti-HER2 monoclonal antibody (mAb), H(2)Mab-19 (IgG(2b), kappa) was developed. Antibody-dependent cellular cytotoxicity (ADCC), complement-dependent cytotoxicity (CDC), and antitumor activity of H(2)Mab-19 were investigated using both breast cancer and oral cancer cell lines. H(2)Mab-19 demonstrated cytotoxicity in BT-474 (a human breast cancer cell line) and HSC-2 or SAS (human oral cancer cell lines). H(2)Mab-19 also possessed both ADCC and CDC activity against BT-474, HSC-2, and SAS cell lines. In comparison to control mouse IgG, H(2)Mab-19 significantly reduced tumor development in BT-474, HSC-2, and SAS xenografts. Collectively, these results suggest that treatment with H(2)Mab-19 may be a useful therapy for patients with HER2-expressing breast and oral cancers.
引用
收藏
页码:846 / 853
页数:8
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