Lorence R M, Katubig B B, Reichard K W, Reyes H M, Phuangsab A, Sassetti M D, Walter R J, Peeples M E
Department of Pathology, Rush-Prebyterian-St. Luke's Medical Center, Chicago, IL 60612-3833.
Cancer Res. 1994 Dec 1;54(23):6017-21.
We have recently demonstrated that a single local injection of the avian pathogen Newcastle disease virus (NDV; strain 73-T) causes complete regression of human neuroblastoma xenografts in athymic mice (R. M. Lorence, K. W. Reichard, B. B. Katubig, H. M. Reyes, A. Phuangsab, B. R. Mitchell, C. J. Cascino, R. J. Walter, and M. E. Peeples. J. Natl. Cancer Inst., 86: 1228-1233, 1994). In this report, we tried to determine if this in vivo antineoplastic effect of NDV extends to human sarcomas. Athymic mice with s.c. HT1080 fibrosarcoma xenografts (7-14 mm) were randomly divided into two groups and treated i.t. with a single injection of either 10(7) plaque-forming units of NDV or phosphate-buffered saline. Complete tumor regression occurred in 8 of 10 mice treated with NDV while unabated tumor growth occurred in all 9 mice treated with phosphate-buffered saline (P < 0.001). To determine if complete tumor regression was long lasting, the 8 mice were monitored for 1 year, during which time no tumor recurred. To test the antitumor effects of NDV on tumors derived from a fresh human sarcoma, a similar experiment was performed in athymic mice using TH15145 synovial sarcoma xenografts at their first and second passages. Of 9 mice with TH15145 xenografts, a single i.t. injection of NDV (10(7) plaque-forming units) caused complete regression of 3 tumors and > 80% regression in 3 more tumors. In contrast, tumors in all 5 mice treated with phosphate-buffered saline exhibited unabated growth (P < 0.03 for > 80% tumor regression). Since HT1080 fibrosarcoma cells express the N-ras oncogene, we explored the effects that transfection of this oncogene has on the sensitivity to NDV. Cultured human fibroblasts that were made tumorigenic following N-ras-transfection were found to be 1000-fold more sensitive to NDV than normal fibroblasts in a cytotoxicity assay. Oncogene expression by the HT1080 fibrosarcoma may therefore contribute to the long-lasting complete regression of this sarcoma following a single local injection of NDV.
我们最近证实,向无胸腺小鼠体内局部单次注射禽源病原体新城疫病毒(NDV;73-T株)可使人类神经母细胞瘤异种移植物完全消退(R.M.洛伦斯、K.W.赖卡德、B.B.卡图比格、H.M.雷耶斯、A.蓬萨布、B.R.米切尔、C.J.卡斯奇诺、R.J.沃尔特和M.E.皮普尔斯,《国家癌症研究所杂志》,86:1228 - 1233,1994年)。在本报告中,我们试图确定NDV的这种体内抗肿瘤作用是否也适用于人类肉瘤。将皮下接种有HT1080纤维肉瘤异种移植物(7 - 14毫米)的无胸腺小鼠随机分为两组,分别经瘤内注射10⁷蚀斑形成单位的NDV或磷酸盐缓冲盐水进行处理。用NDV处理的10只小鼠中有8只肿瘤完全消退,而用磷酸盐缓冲盐水处理的所有9只小鼠肿瘤均持续生长(P < 0.001)。为确定肿瘤完全消退是否持久,对这8只小鼠进行了为期1年的监测,在此期间无肿瘤复发。为测试NDV对源自新鲜人类肉瘤的肿瘤的抗肿瘤作用,在无胸腺小鼠中使用传代1次和2次的TH15145滑膜肉瘤异种移植物进行了类似实验。在9只接种TH15145异种移植物的小鼠中,单次瘤内注射NDV(10⁷蚀斑形成单位)使3个肿瘤完全消退,另有三个肿瘤消退超过80%。相比之下,用磷酸盐缓冲盐水处理的所有5只小鼠的肿瘤均持续生长(肿瘤消退超过80%时P < 0.03)。由于HT1080纤维肉瘤细胞表达N-ras癌基因,我们研究了该癌基因转染对NDV敏感性的影响。在细胞毒性试验中,发现经N-ras转染后具有致瘤性的培养人成纤维细胞对NDV的敏感性比正常成纤维细胞高1000倍。因此,HT1080纤维肉瘤的癌基因表达可能是该肉瘤经单次局部注射NDV后实现持久完全消退的原因。