SPATIAL AND TEMPORAL CONTROL OF GENE-THERAPY USING IONIZING-RADIATION

被引:287
作者
HALLAHAN, DE
MAUCERI, HJ
SEUNG, LP
DUNPHY, EJ
WAYNE, JD
HANNA, NN
TOLEDANO, A
HELLMAN, S
KUFE, DW
WEICHSELBAUM, RR
机构
[1] UNIV CHICAGO,DEPT RADIAT & CELLULAR ONCOL,CHICAGO,IL 60637
[2] UNIV CHICAGO,PRITZKER SCH MED,CHICAGO,IL 60637
[3] UNIV CHICAGO,DEPT SURG,CHICAGO,IL 60637
[4] UNIV CHICAGO,DEPT ANESTHESIA & CRIT CARE,CHICAGO,IL 60637
[5] DANA FARBER CANC INST,DIV CANC PHARMACOL,BOSTON,MA 02115
关键词
D O I
10.1038/nm0895-786
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
Activation of transcription of the Egr-1 gene by X-rays is regulated by the promoter region of this gene. We linked the radiation-inducible promoter region of the Egr-1 gene to the gene encoding the radiosensitizing and tumoricidal cytokine, tumour necrosis factor-alpha (TNF-alpha) and used a replication-deficient adenovirus to deliver the Egr-TNF construct to human tumours growing in nude mice. Combined treatment with AdS.EgrTNF and 5,000 cGy (rad) resulted in increased intratumoral TNF-a production and increased tumour control compared with treatment with Ad5.Egr-TNF alone or with radiation alone. The increase in tumour control was achieved without an increase in normal tissue damage when compared to tissue injury from radiation alone. Control of gene transcription by ionizing radiation in vivo represents a novel method of spatial and temporal regulation of gene-based medical treatments.
引用
收藏
页码:786 / 791
页数:6
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