Intrabody-based approaches to cancer therapy: Status and prospects

被引:33
作者
Williams, BR [1 ]
Zhu, ZP [1 ]
机构
[1] ImClone Syst Inc, Dept Antibody Technol, New York, NY 10014 USA
关键词
D O I
10.2174/092986706776872899
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
Continuing developments from the study of cancer at the molecular level are yielding increasing numbers of targets that may be used for therapeutic intervention. Advances in the field of antibody engineering over the past several decades have given scientists the capability of directing the highly specific interaction of antibodies with antigens inward, to the intracellular compartments of living cells. These intracellular antibodies, i.e., intrabodies, are being developed to bind to, neutralize, or modify the function or localization of cancer-related targets and thereby affect the malignant phenotype. This has resulted in a promising new tool for the study and treatment of cancer. Due to recent advances in the development of the antibody engineering technologies, increasing numbers of intrabodies are being exploited to a growing list of cancer-related, as well as other disease targets. There are still, however, many technical issues, particularly related to clinical applications of the intrabodics, that must be addressed before the full promise of this class of therapeutic agent is realized. This review will focus on the recent progress in the generation and use of intrabodies in the field of oncology. The technical issues associated with their further development will also be discussed.
引用
收藏
页码:1473 / 1480
页数:8
相关论文
共 109 条
[1]   Monoclonal antibody therapy of cancer [J].
Adams, GP ;
Weiner, LM .
NATURE BIOTECHNOLOGY, 2005, 23 (09) :1147-1157
[2]  
Alvarez RD, 2000, CLIN CANCER RES, V6, P3081
[3]   INTRACELLULAR NEUTRALIZATION OF SV40 TUMOR-ANTIGENS FOLLOWING MICRO-INJECTION OF SPECIFIC ANTIBODY [J].
ANTMAN, KH ;
LIVINGSTON, DM .
CELL, 1980, 19 (03) :627-635
[4]   RNA interference may be more potent than antisense RNA in human cancer cell lines [J].
Aoki, Y ;
Cioca, DP ;
Oidaira, H ;
Kamiya, J ;
Kiyosawa, K .
CLINICAL AND EXPERIMENTAL PHARMACOLOGY AND PHYSIOLOGY, 2003, 30 (1-2) :96-102
[5]   Role of tyrosine kinase inhibitors in cancer therapy [J].
Arora, A ;
Scholar, EM .
JOURNAL OF PHARMACOLOGY AND EXPERIMENTAL THERAPEUTICS, 2005, 315 (03) :971-979
[6]   Polyreactive anti-DNA monoclonal antibodies and a derived peptide as vectors for the intracytoplasmic and intranuclear translocation of macromolecules [J].
Avrameas, A ;
Ternynck, T ;
Nato, F ;
Buttin, G ;
Avrameas, S .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (10) :5601-5606
[7]   Escherichia coli maltose-binding protein as a molecular chaperone for recombinant intracellular cytoplasmic single-chain antibodies [J].
Bach, H ;
Mazor, Y ;
Shaky, S ;
Shoham-Lev, A ;
Berdichevsky, Y ;
Gutnick, DL ;
Benhar, I .
JOURNAL OF MOLECULAR BIOLOGY, 2001, 312 (01) :79-93
[8]   AUTOCRINE INHIBITION OF THE EPIDERMAL GROWTH-FACTOR RECEPTOR BY INTRACELLULAR EXPRESSION OF A SINGLE-CHAIN ANTIBODY [J].
BEERLI, RR ;
WELS, W ;
HYNES, NE .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1994, 204 (02) :666-672
[9]  
BEERLI RR, 1994, J BIOL CHEM, V269, P23931
[10]   Targeted cancer therapy using radiolabeled monoclonal antibodies [J].
Bethge, WA ;
Sandmaier, BM .
TECHNOLOGY IN CANCER RESEARCH & TREATMENT, 2005, 4 (04) :393-405