作者: D. D. Bigner , M. H. Werner , S. H. Bigner , P. A. Humphrey
DOI: 10.1007/BF00687431
关键词: In vivo 、 Growth factor receptor inhibitor 、 Cancer research 、 Molecular biology 、 Monoclonal antibody 、 Epidermal growth factor receptor 、 Cell division 、 Epidermal growth factor 、 Biology 、 Receptor 、 Cell
摘要: Epidermal growth factor (EGF) has been shown to stimulate DNA synthesis and cell division in normal glia. At least half of malignant human gliomas (MHG) express high levels the EGF receptor (EGFR), which are above those detected brain. The demonstration that antibodies against EGFR inhibit squamous carcinoma line A-431, with large numbers EGFR, vitro vivo raises possibility these agents could be used therapeutically either alone or conjugated other agents. We have measured effects an anti-EGFR monoclonal antibody, 528 (Ab-528), on four well-characterized glioma lines, D-263 MG, D-247 U-343 MGa Cl 2∶6, D-37 2.9×104, 1.5×105, 8.6×105 1.59×106 EGFRs per cell, respectively. significantly increased number MG by 65% 74%, respectively, had no effect decreased 2∶6 39%. was inhibited 19% Ab-528, but Ab-528 MHG lines. all EGF-mediated effects. These studies demonstrate that, although little antiproliferative activity MGH, it successfully competes reduce biological EGF-EGFR binding. Therefore, this antibody potentially target radioisotopes via for diagnosis therapy.