The anti-EGFR monoclonal antibody blocks cisplatin-induced activation of EGFR signaling mediated by HB-EGF |
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Authors: | Takeshi Yoshida Tsutomu Iwasa Kazuhiko Nakagawa |
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Affiliation: | a Department of Medical Oncology, Kinki University School of Medicine, 377-2 Ohno-higashi, Osaka-Sayama, Osaka 589-8511, Japan b Kinki University School of Medicine, Sakai Hospital, 2-7-1 Harayamadai, Minami-ku Sakai, Osaka 590-0132, Japan |
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Abstract: | Cisplatin is a key agent in combination chemotherapy for various types of solid tumor. We now show that cisplatin activates signaling by the epidermal growth factor receptor (EGFR) by inducing cleavage of heparin-binding epidermal growth factor-like growth factor (HB-EGF). Matuzumab, a monoclonal antibody to EGFR, inhibited cisplatin-induced EGFR signaling, likely through competition with the soluble form of HB-EGF for binding to EGFR. Matuzumab enhanced the antitumor effect of cisplatin in nude mice harboring human non-small cell lung cancer xenografts. Our findings shed light on the mechanism by which monoclonal antibodies to EGFR might augment the efficacy of cisplatin. |
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Keywords: | EGF, epidermal growth factor EGFR, EGF receptor mAb, monoclonal antibody NSCLC, non-small cell lung cancer HB-EGF, heparin-binding EGF-like growth factor HRP, horseradish peroxidase TUNEL, terminal deoxynucleotidyl transferase-mediated dUTP nick-end labeling |
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