Combining a targeted radiotherapy and gene therapy approach for adenocarcinoma of prostate

被引:0
作者
N E Fullerton
M Boyd
R J Mairs
W N Keith
O Alderwish
M M Brown
A Livingstone
D Kirk
机构
[1] Centre for Oncology & Applied Pharmacology,Department of Urology
[2] University of Glasgow,undefined
[3] Cancer Research UK Beatson Laboratories,undefined
[4] Gartnavel General Hospital,undefined
来源
Prostate Cancer and Prostatic Diseases | 2004年 / 7卷
关键词
gene therapy; targeted radiotherapy; [; I]MIBG; bystander effect; telomerase;
D O I
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中图分类号
学科分类号
摘要
A targeted radiotherapy/gene therapy approach for prostate cancer, using the radiopharmaceutical [131I]meta-iodobenzylguanidine ([131I]MIBG), would restrict the effects of radiotherapy to malignant cells, thereby increasing efficacy and decreasing morbidity of radiotherapy. Prostate cancer cells were transfected with a transgene encoding the noradrenaline transporter (NAT) under the control of tumour-specific telomerase promoters, enabling them to actively take up [131I]MIBG. This led to tumour-specific cell kill. This strategy has the advantage of generating a radiological bystander effect, leading to the destruction of neighbouring tumour cells that have escaped transfection. This targeted approach could be a promising tumour-specific treatment option for prostate cancer.
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页码:355 / 363
页数:8
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