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Updated: Feb 9, 2026

Generation of Induced Pluripotent Stem Cells from Human Melanoma Tumor-infiltrating Lymphocytes
Published on: November 11, 2016
An Agonistic Antibody to EPHA2 Exhibits Antitumor Effects on Human Melanoma Cells
Atsushi Sakamoto1, Kazunori Kato2,3, Toshio Hasegawa1
1Department of Dermatology and Allergology, Juntendo University Graduate School of Medicine, Tokyo, Japan.
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.
Insights
Antibodies targeting EPH receptor A2 (EPHA2) show promise for melanoma treatment. One antibody, SHM16, inhibited cancer cell migration and, when conjugated to toxins, caused significant cell death.
Area of Science:
- Oncology
- Immunology
- Molecular Biology
Background:
- EPH receptor A2 (EPHA2) is overexpressed in aggressive human cancers.
- EPHA2 is a potential target for antibody-based cancer therapies.
Purpose of the Study:
- To evaluate the therapeutic potential of EPHA2 antibodies against melanoma.
- To investigate EPHA2 as a therapeutic target in melanoma treatment.
Main Methods:
- Generated three monoclonal antibodies (mAbs) against EPHA2.
- Assessed EPHA2 expression using flow cytometry.
- Evaluated anti-metastatic effects via wound scratch and invasion assays.
- Tested immunotoxins composed of EPHA2 mAbs conjugated to toxins.
Main Results:
- All tested melanoma cell lines expressed EPHA2.
- One EPHA2 mAb, SHM16, inhibited melanoma cell migration and invasion, similar to its natural ligand ephrin-A1.
- SHM16-based immunotoxins demonstrated significant melanoma cell growth inhibition and cytotoxicity.
Conclusions:
- EPHA2 is a promising therapeutic target for melanoma.
- An agonistic antibody to EPHA2, SHM16, exhibits significant anti-melanoma potential.
- EPHA2-targeted immunotoxins offer a viable therapeutic strategy for melanoma.
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