Conditional gene targeting for cancer gene therapy

被引:59
作者
Haviv, YS
Curiel, DT
机构
[1] Univ Alabama, Div Human Gene Therapy, Dept Med, Birmingham, AL 35294 USA
[2] Univ Alabama, Dept Surg, Birmingham, AL 35294 USA
[3] Univ Alabama, Dept Pathol, Birmingham, AL 35294 USA
[4] Univ Alabama, Gene Therapy Ctr, Birmingham, AL 35294 USA
关键词
cancer gene therapy; gene expression; regulatory elements;
D O I
10.1016/S0169-409X(01)00225-3
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Current treatment of solid tumors is limited by severe adverse effects, resulting in a narrow therapeutic index. Therefore, cancer gene therapy has emerged as a targeted approach that would significantly reduce undesired side effects in normal tissues. This approach requires a clear understanding of the molecular biology of both the malignant clone and the biological vectors that serve as vehicles to target cancer cells. In this review we discuss novel approaches for conditional gene expression in cancer cells. Targeting transgene expression to malignant tissues requires the use of specific regulatory elements including promoters based on tumor biology, tissue-specific promoters and inducible regulatory elements. We also discuss the regulation of both replication and transgene expression by conditionally-replicative viruses. These approaches have the potential to restrict the expression of transgenes exclusively to tissues of interest and thereby to increase the therapeutic index of future vectors for cancer gene therapy. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:135 / 154
页数:20
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