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在肾细胞癌小鼠模型中,端粒酶特异性、复制型腺病毒(OBP-301)和 IL-2 联合治疗具有强大的抗肿瘤作用。

Potent antitumor effects of combined therapy with a telomerase-specific, replication-competent adenovirus (OBP-301) and IL-2 in a mouse model of renal cell carcinoma.

机构信息

Department of Urology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, 2-5-1 Shikata-cho, Okayama, Japan.

出版信息

Cancer Gene Ther. 2010 Jul;17(7):484-91. doi: 10.1038/cgt.2010.5. Epub 2010 Feb 19.

DOI:10.1038/cgt.2010.5
PMID:20168351
Abstract

OBP-301 (a telomerase-specific, replication-competent adenovirus with hTERT promoter) was constructed in a previous study and it showed a strong anticancer effect by inducing cell lysis in human lung and prostate cancer cells. This study investigated the effectiveness of a combination therapy of OBP-301 and interleukin-2 (IL-2) in a mouse model of renal cell carcinoma (RCC). The cell-killing effect of OBP-301 was confirmed in vitro in the RENCA cancer cells. In in vivo experiment, luciferase-expressing RENCA cells were implanted in the left kidney and lung of BALB/c mice to prepare the RCC metastatic model. The animals were randomly divided into four treatment groups: PBS, IL-2 alone, OBP-301 alone and the combination. The analyses of orthotopic tumor weight, lung metastasis and luciferin-stained tumor images 14 days after each treatment showed significant tumor growth inhibition in the combination group in comparison with that in the OBP-301- or IL-2-treated groups. In addition, the percentage of regulatory T-cells (Tregs) in the combination group was significantly suppressed in comparison with that in the PBS and single-agent treatment groups. The outcomes of this study suggest that tumor-specific oncolytic immunovirotherapy may become an attractive strategy for the treatment of human RCC.

摘要

OBP-301(一种具有 hTERT 启动子的端粒酶特异性、复制能力的腺病毒)在之前的研究中构建,它通过诱导人肺和前列腺癌细胞裂解显示出强烈的抗癌作用。本研究探讨了 OBP-301 和白细胞介素-2(IL-2)联合治疗肾细胞癌(RCC)小鼠模型的有效性。在体外实验中,在 RENCA 癌细胞中证实了 OBP-301 的细胞杀伤作用。在体内实验中,将表达荧光素酶的 RENCA 细胞植入 BALB/c 小鼠的左肾和肺中,制备 RCC 转移模型。动物随机分为四组:PBS、IL-2 单独、OBP-301 单独和联合治疗组。在每种治疗后 14 天分析原位肿瘤重量、肺转移和荧光素标记肿瘤图像显示,与 OBP-301 或 IL-2 治疗组相比,联合治疗组的肿瘤生长明显受到抑制。此外,与 PBS 和单药治疗组相比,联合治疗组的调节性 T 细胞(Tregs)百分比明显受到抑制。本研究的结果表明,肿瘤特异性溶瘤免疫治疗可能成为治疗人类 RCC 的一种有吸引力的策略。

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