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The anti-EGFR monoclonal antibody blocks cisplatin-induced activation of EGFR signaling mediated by HB-EGF
Authors:Takeshi Yoshida  Tsutomu Iwasa  Kazuhiko Nakagawa
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
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.
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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