Sym004: A Novel Synergistic Anti-Epidermal Growth Factor Receptor Antibody Mixture with Superior Anticancer Efficacy

被引:177
作者
Pedersen, Mikkel Wandahl [1 ]
Jacobsen, Helle Jane [1 ]
Koefoed, Klaus [1 ]
Hey, Adam [1 ]
Pyke, Charles [1 ]
Haurum, John Sorensen [1 ]
Kragh, Michael [1 ]
机构
[1] Symphogen AS, Dept Antibody Pharmacol, DK-2800 Lyngby, Denmark
关键词
MONOCLONAL-ANTIBODY; FACTOR EGF; ACTIVATION; INHIBITION; COMBINATIONS; COMPLEXES; CELLS; GENE;
D O I
10.1158/0008-5472.CAN-09-1417
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Epidermal growth factor receptor (EGFR) is a validated therapeutic target in cancer and EGFR antagonists with greater effectiveness than existing clinical agents remain of interest. Here, we report a novel approach based on Sym004, a mixture of two anti-EGFR monoclonal antibodies directed against distinct nonoverlapping epitopes in EGFR extracellular domain III. Like anti-EGFR monoclonal antibodies in current clinical use, Sym004 inhibits cancer cell growth and survival by blocking ligand-binding receptor activation and phosphorylation and downstream receptor signaling. However, unlike the other antibodies, Sym004 induces rapid and efficient removal of the receptor from the cancer cell surface by triggering EGFR internalization and degradation. Compared with reference anti-EGFR monoclonal antibodies, Sym004 exhibited more pronounced growth inhibition in vitro and superior efficacy in vivo. Together, these findings illustrate a strategy to target EGFR more effectively than existing clinical antibodies. Cancer Res; 70(2); 588-97. (C)2010 AACR.
引用
收藏
页码:588 / 597
页数:10
相关论文
共 26 条
[1]  
Arteaga CL, 2001, J CLIN ONCOL, V19, p32S
[2]   Epidermal growth factor and membrane trafficking: EGF receptor activation of endocytosis requires Rab5a [J].
Barbieri, MA ;
Roberts, RL ;
Gumusboga, A ;
Highfield, H ;
Alvarez-Dominguez, C ;
Wells, A ;
Stahl, PD .
JOURNAL OF CELL BIOLOGY, 2000, 151 (03) :539-550
[3]   Persistent elimination of ErbB-2/HER2-overexpressing tumors using combinations of monoclonal antibodies: Relevance of receptor endocytosis [J].
Ben-Kasus, Tsipi ;
Schechter, Bilha ;
Lavi, Sara ;
Yarden, Yosef ;
Sela, Michael .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2009, 106 (09) :3294-3299
[4]   HETEROGENEITY OF HUMAN-COLON CARCINOMA [J].
BRATTAIN, MG ;
LEVINE, AE ;
CHAKRABARTY, S ;
YEOMAN, LC ;
WILLSON, JKV ;
LONG, B .
CANCER AND METASTASIS REVIEWS, 1984, 3 (03) :177-191
[5]   Amphiregulin acts as an autocrine growth factor in two human polarizing colon cancer lines that exhibit domain selective EGF receptor mitogenesis [J].
Damstrup, L ;
Kuwada, SK ;
Dempsey, PJ ;
Brown, CL ;
Hawkey, CJ ;
Poulsen, HS ;
Wiley, HS ;
Coffey, RJ .
BRITISH JOURNAL OF CANCER, 1999, 80 (07) :1012-1019
[6]   Epidermal growth factor (EGF) receptor kinase-independent signaling by EGF [J].
Deb, TB ;
Su, L ;
Wong, L ;
Bonvini, E ;
Wells, A ;
David, M ;
Johnson, GR .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (18) :15554-15560
[7]   Synergistic down-regulation of receptor tyrosine kinases by combinations of mAbs: Implications for cancer immunotherapy [J].
Friedman, LM ;
Rinon, A ;
Schechter, B ;
Lyass, L ;
Lavi, S ;
Bacus, SS ;
Sela, M ;
Yarden, Y .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (06) :1915-1920
[8]  
Hirabayashi K, 1999, CANCER RES, V59, P4325
[9]   Differential regulation of EGF receptor internalization and degradation by multiubiquitination within the kinase domain [J].
Huang, FT ;
Kirkpatrick, D ;
Jiang, XJ ;
Gygi, S ;
Sorkin, A .
MOLECULAR CELL, 2006, 21 (06) :737-748
[10]   Antibody-dependent cellular cytotoxicity mediated by cetuximab against lung cancer cell lines [J].
Kurai, Jun ;
Chikumi, Hiroki ;
Hashimoto, Kiyoshi ;
Yamaguchi, Kosuke ;
Yamasaki, Akira ;
Sako, Takanori ;
Touge, Hirokazu ;
Makino, Haruhiko ;
Takata, Miyako ;
Miyata, Masanori ;
Nakamoto, Masaki ;
Burioka, Naoto ;
Shimizu, Eiji .
CLINICAL CANCER RESEARCH, 2007, 13 (05) :1552-1561