A fully human recombinant IgG-like bispecific antibody to both the epidermal growth factor receptor and the insulin-like growth factor receptor for enhanced antitumor activity

被引:141
作者
Lu, D
Zhang, HF
Koo, H
Tonra, J
Balderes, P
Prewett, M
Corcoran, E
Mangalampalli, V
Bassi, R
Anselma, D
Patel, D
Kang, XQ
Ludwig, DL
Hicklin, DJ
Bohlen, P
Witte, L
Zhu, ZP
机构
[1] ImClone Syst Inc, Dept Antibody Technol, New York, NY 10014 USA
[2] ImClone Syst Inc, Dept Mol & Cell Biol, New York, NY 10014 USA
[3] ImClone Syst Inc, Dept Expt Therapeut, New York, NY 10014 USA
[4] ImClone Syst Inc, Dept Prot Sci, New York, NY 10014 USA
[5] ImClone Syst Inc, Res Dept, New York, NY 10014 USA
关键词
D O I
10.1074/jbc.M500815200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Both the epidermal growth factor receptor ( EGFR) and the insulin-like growth factor receptor (IGFR) have been implicated in the tumorigenesis of a variety of cancers. Here we propose that simultaneous targeting of both receptors with a bispecific antibody would lead to enhanced antitumor activity. To this end, we produced a recombinant human IgG-like bispecific antibody, a Di-diabody, using the variable regions from two antagonistic antibodies: IMC-11F8 to EGFR and IMC-A12 to IGFR. The Di-diabody binds to both EGFR and IGFR and effectively blocked both EGF- and IGF-stimulated receptor activation and tumor cell proliferation. The Di-diabody also inherited the biological properties from both of its parent antibodies; it triggers rapid and significant IGFR internalization and degradation and mediates effective antibody-dependent cellular cytotoxicity in a variety of tumor cells. Finally, the Di-diabody strongly inhibited the growth of two different human tumor xenografts in vivo. Our results underscore the benefits of simultaneous targeting of two tumor targets with bispecific antibodies.
引用
收藏
页码:19665 / 19672
页数:8
相关论文
共 51 条
[1]   Novel tetravalent and bispecific IgG-like antibody molecules combining single-chain diabodies with the immunoglobulin γl Fc or CH3 region [J].
Alt, M ;
Müller, R ;
Kontermann, RE .
FEBS LETTERS, 1999, 454 (1-2) :90-94
[2]  
[Anonymous], P AM ASS CANC RES
[3]   Targeting HERI/EGFR: A molecular approach to cancer therapy [J].
Arteaga, C .
SEMINARS IN ONCOLOGY, 2003, 30 (03) :3-14
[4]   Overview of epidermal growth factor receptor biology and its role as a therapeutic target in human neoplasia [J].
Arteaga, CL .
SEMINARS IN ONCOLOGY, 2002, 29 (05) :3-9
[5]   Herceptin® alone or in combination with chemotherapy in the treatment of HER2-positive metastatic breast cancer:: Pivotal trials [J].
Baselga, J .
ONCOLOGY, 2001, 61 :14-21
[6]   The IGF-I receptor in cancer research [J].
Baserga, R .
EXPERIMENTAL CELL RESEARCH, 1999, 253 (01) :1-6
[7]  
Benini S, 2001, CLIN CANCER RES, V7, P1790
[8]  
Bonner JA, 2004, J CLIN ONCOL, V22, p489S
[9]   The anti-proliferative effect of suramin towards tamoxifen-sensitive and resistant human breast cancer cell lines in relation to expression of receptors for epidermal growth factor and insulin-like growth factor-I: Growth stimulation in the presence of tamoxifen [J].
Boylan, M ;
van den Berg, HW ;
Lynch, M .
ANNALS OF ONCOLOGY, 1998, 9 (02) :205-211
[10]  
Burtrum D, 2003, CANCER RES, V63, P8912