Kim J H, Kim S H, Brown S L, Freytag S O
Henry Ford Hospital, Department of Radiation Oncology, Detroit, Michigan 48202-4689.
Cancer Res. 1994 Dec 1;54(23):6053-6.
The activation of antiviral drugs as a consequence of thymidine kinase expression has been shown in recent years to have potential as a treatment for malignant tumors. It was hypothesized that the property of the drugs that make them effective against viruses and proliferating cells, namely their ability to interfere with the integrity of the DNA, may be exploited to sensitize cells to radiation damage. The antiviral drug, BVdUrd, structurally a pyrimidine analogue, was found to enhance selectively the radiation cytotoxicity of human tumor cells transduced with the HSV-tk thymidine kinase gene. Human glioma cells from the U-251 lineage transduced with HSV-tk and exposed to 40 micrograms/ml of BVdUrd for 24 h prior to irradiation were more sensitive to radiation compared with control cells under the same conditions; the sensitization enhancement ratio was 1.9. The results suggest that the addition of radiation will improve the effectiveness of HSV-tk gene therapy for the treatment of brain tumors.
近年来已表明,由于胸苷激酶表达而激活的抗病毒药物具有作为恶性肿瘤治疗方法的潜力。据推测,这些药物对病毒和增殖细胞有效的特性,即它们干扰DNA完整性的能力,可被利用来使细胞对辐射损伤敏感。抗病毒药物BVdUrd在结构上是一种嘧啶类似物,已发现它能选择性增强用单纯疱疹病毒胸苷激酶(HSV-tk)基因转导的人肿瘤细胞的辐射细胞毒性。在用HSV-tk转导并在照射前24小时暴露于40微克/毫升BVdUrd的U-251谱系的人胶质瘤细胞,与相同条件下的对照细胞相比,对辐射更敏感;增敏增强比为1.9。结果表明,添加辐射将提高HSV-tk基因疗法治疗脑肿瘤的有效性。