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前体药物癌症基因治疗。

Prodrug cancer gene therapy.

作者信息

Altaner Cestmir

机构信息

Cancer Research Institute, Slovak Academy of Sciences, Vlarska 7, 83391 Bratislava, Slovakia.

出版信息

Cancer Lett. 2008 Nov 8;270(2):191-201. doi: 10.1016/j.canlet.2008.04.023. Epub 2008 May 27.

Abstract

There is no effective treatment for late stage and metastatic cancers of colorectal, prostate, pancreatic, breast, glioblastoma and melanoma cancers. Novel treatment modalities are needed for these late stage patients because cytotoxic chemotherapy offers only palliation, usually accompanied with systemic toxicities and poor quality of life. Gene directed enzyme prodrug therapy (GDEPT), which concentrates the cytotoxic effect in the tumor site may be one alternative. This review provides an explanation of the GDEPT principle, focusing on the development, application and potential of various GDEPTs. Current gene therapy limitations are in efficient expression of the therapeutic gene and in tumor-specific targeting. Therefore, the current status of research related to the enhancement of in situ GDEPT delivery and tumor-specific targeting of vectors is assessed. Finally, GDEPT versions of stem cell based gene therapy as another potential treatment modality for progressed tumors and metastases are discussed. Combinations of traditional, targeted, and stem cell directed gene therapy could significantly advance the treatment of cancer.

摘要

对于结直肠癌、前列腺癌、胰腺癌、乳腺癌、胶质母细胞瘤和黑色素瘤的晚期及转移性癌症,目前尚无有效的治疗方法。由于细胞毒性化疗仅能提供姑息治疗,通常伴有全身毒性且生活质量较差,因此这些晚期患者需要新的治疗方式。基因导向酶前药疗法(GDEPT)可将细胞毒性作用集中于肿瘤部位,可能是一种选择。本综述对GDEPT原理进行了解释,重点关注各种GDEPT的发展、应用和潜力。当前基因治疗的局限性在于治疗基因的有效表达和肿瘤特异性靶向。因此,评估了与增强原位GDEPT递送和载体的肿瘤特异性靶向相关的研究现状。最后,讨论了基于干细胞的基因治疗的GDEPT版本作为进展期肿瘤和转移瘤的另一种潜在治疗方式。传统、靶向和干细胞导向基因治疗的联合应用可显著推进癌症治疗。

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