Harrison G S, Glode L M
Department of Medicine, School of Medicine, University of Colorado, Health Sciences Center, Denver, USA.
Oncology (Williston Park). 1997 Jun;11(6):845-50, 856; discussion 856-8, 861.
Gene therapy for prostate cancer faces hurdles similar to those being encountered for other cancers and nonmalignant processes. The greatest obstacle is the identification of efficient delivery systems, since numerous animal models and cell culture systems have shown potential efficacy when most cells express the introduced genetic material. Early prostate cancers are easily accessible to gene vector introduction, and the predictable metastatic patterns of this cancer may offer additional advantages for gene therapy. This article reviews gene vectors and gene products, as well as ongoing trials of gene therapy that have recently begun in prostate cancer.
前列腺癌的基因治疗面临着与其他癌症及非恶性疾病治疗中所遇到的类似障碍。最大的障碍是确定有效的递送系统,因为众多动物模型和细胞培养系统已表明,当大多数细胞表达导入的遗传物质时具有潜在疗效。早期前列腺癌易于进行基因载体导入,且这种癌症可预测的转移模式可能为基因治疗带来额外优势。本文综述了基因载体、基因产物,以及最近开始的前列腺癌基因治疗临床试验。