An Agonistic Antibody to EPHA2 Exhibits Antitumor Effects on Human Melanoma Cells

被引:21
|
作者
Sakamoto, Atsushi [1 ]
Kato, Kazunori [2 ,3 ]
Hasegawa, Toshio [1 ]
Ikeda, Shigaku [1 ,2 ]
机构
[1] Juntendo Univ, Grad Sch Med, Dept Dermatol & Allergol, Tokyo, Japan
[2] Juntendo Univ, Grad Sch Med, Atopy Res Ctr, Tokyo, Japan
[3] Toyo Univ, Dept Biomed Engn, 2100 Kujirai, Kawagoe, Saitama 3508585, Japan
关键词
EPHA2; melanoma; monoclonal antibody; immunotoxin; invasion; GENE-THERAPY; IN-VIVO; CANCER; RECEPTOR; EPHRIN; INHIBITION; GROWTH; MAPK; IMMUNOTHERAPY; ANGIOGENESIS;
D O I
10.21873/anticanres.12592
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background/Aim: EPH receptor A2 (EPHA2) is highly expressed in aggressive types of human cancer, and is expected to be an excellent target molecule for antibody treatments. In this study, we investigated the therapeutic potential of antibody to EPHA2 against melanoma in vitro. Materials and Methods: We generated three monoclonal antibodies (mAbs) to EPHA2 and examined cell-surface expression by flow cytometry. To investigate the ability to inhibit tumor cell migration therapy with mAbs to EPHA2, we performed a wound scratch assay and invasion assay. We investigated the therapeutic effects of immunotoxins consisting of toxin-conjugated EPHA2 mAbs. Results: All human melanoma cell lines studied expressed EPHA2. Like natural ligand ephrin-A1, one of EPHA2 mAbs, SHM16, inhibited metastatic behavior of cells, such as migration and invasion. In addition, drastic growth inhibition and cytotoxicity were found using immunotoxin-conjugated SHM16. Conclusion: These observations indicate a promising role for EPHA2 as a target in antibody treatments for melanoma, and demonstrate the potential therapeutic effects of an agonistic antibody to EPHA2.
引用
收藏
页码:3273 / 3282
页数:10
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