Intracellular antibody-caspase-mediated cell killing: An approach for application in cancer therapy

被引:65
作者
Tse, E [1 ]
Rabbitts, TH [1 ]
机构
[1] MRC, Mol Biol Lab, Div Prot & Nucleic Acid Chem, Cambridge CB2 2QH, England
关键词
single-chain Fv; gene therapy; apoptosis; chromosomal translocation; leukemia;
D O I
10.1073/pnas.97.22.12266
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Antibodies have been expressed inside cells in an attempt to ablate the function of oncogene products. To make intracellular antibodies more generally applicable and effective in cancer therapy, we have: devised a method in which programmed cell death or apoptosis can be triggered by specific antibody-antigen interaction, When intracellular antibodies are linked to caspase 3, the "executioner" in the apoptosis pathway, and bind to the target antigen, the caspase 3 moieties are self-activated and thereby induce cell killing. We have used this strategy in a model system with two pairs:of intracellular antibodies and antigens. In vivo coexpression of an antibody-caspase 3 fusion with its antigenic target induced apoptosis that was specific for antibody, antigen, and active caspase 3. Moreover, the antibody-caspase 3 fusion protein was not toxic to cells in the absence of antigen. Therefore, intracellular antibody-mediated apoptosis should be useful as a specific therapeutic approach for the treatment of cancers, a situation where target cell killing is required.
引用
收藏
页码:12266 / 12271
页数:6
相关论文
共 29 条
[11]   SEGMENTAL AND DEVELOPMENTAL REGULATION OF A PRESUMPTIVE T-CELL ONCOGENE IN THE CENTRAL-NERVOUS-SYSTEM [J].
GREENBERG, JM ;
BOEHM, T ;
SOFRONIEW, MV ;
KEYNES, RJ ;
BARTON, SC ;
NORRIS, ML ;
SURANI, MA ;
SPILLANTINI, MG ;
RABBITTS, TH .
NATURE, 1990, 344 (6262) :158-160
[12]   THE DOMINATING EFFECT OF MUTANT P53 [J].
HANN, BC ;
LANE, DP .
NATURE GENETICS, 1995, 9 (03) :221-222
[13]   P53 MUTATIONS IN HUMAN CANCERS [J].
HOLLSTEIN, M ;
SIDRANSKY, D ;
VOGELSTEIN, B ;
HARRIS, CC .
SCIENCE, 1991, 253 (5015) :49-53
[14]   3-DIMENSIONAL STRUCTURE OF BETA-GALACTOSIDASE FROM ESCHERICHIA-COLI [J].
JACOBSON, RH ;
ZHANG, XJ ;
DUBOSE, RF ;
MATTHEWS, BW .
NATURE, 1994, 369 (6483) :761-766
[15]   Intracellular expression of single-chain variable fragments to inhibit early stages of the viral life cycle by targeting human immunodeficiency virus type 1 integrase [J].
LevyMintz, P ;
Duan, LX ;
Zhang, HZ ;
Hu, BC ;
Dornadula, G ;
Zhu, MH ;
Kulkosky, J ;
BizubBender, D ;
Skalka, AM ;
Pomerantz, RJ .
JOURNAL OF VIROLOGY, 1996, 70 (12) :8821-8832
[16]   Synthetic activation of caspases: Artificial death switches [J].
MacCorkle, RA ;
Freeman, KW ;
Spencer, DM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (07) :3655-3660
[17]   Expression of an antibody fragment at high levels in the bacterial cytoplasm [J].
Martineau, P ;
Jones, P ;
Winter, G .
JOURNAL OF MOLECULAR BIOLOGY, 1998, 280 (01) :117-127
[18]   PEF-BOS, A POWERFUL MAMMALIAN EXPRESSION VECTOR [J].
MIZUSHIMA, S ;
NAGATA, S .
NUCLEIC ACIDS RESEARCH, 1990, 18 (17) :5322-5322
[19]   Antibody scFv fragments without disulfide bonds made by molecular evolution [J].
Proba, K ;
Wörn, A ;
Honegger, A ;
Plückthun, A .
JOURNAL OF MOLECULAR BIOLOGY, 1998, 275 (02) :245-253
[20]   CHROMOSOMAL TRANSLOCATIONS IN HUMAN CANCER [J].
RABBITTS, TH .
NATURE, 1994, 372 (6502) :143-149