Takahashi K, Watanuki Y, Yamazaki M, Abe S
Research Development Corporation of Japan, Tokyo.
Br J Cancer. 1988 Feb;57(2):170-3. doi: 10.1038/bjc.1988.35.
When an antitumour mannoglucan prepared from Microellobosporia grisea, MGA was administered i.v. to C3H/He mice bearing the solid MH134 hepatoma, a cytotoxic factor was induced that was detectable in the tumour homogenate by an 8 h cytolysis assay against L-929 fibroblasts. Without MGA treatment, the cytotoxic factor was not detectable in the tumour homogenate. MGA induced the cytotoxic factor in tumour tissue specifically, its level reaching a maximum (24 U ml-1) 3 h after administration of MGA: little if any cytotoxic factor was detectable in homogenates of normal tissues or sera after MGA-treatment. The molecular size of the cytotoxic factor was estimated to be 70-80 kD by gel filtration. It seemed to be a type of tumour necrosis factor because its activity was inhibited by antiserum against murine tumour necrosis factor. From these results, the selective induction of the cytotoxic factor was concluded to be important in the mechanism of the antitumour activity of MGA.
当将由灰微球孢制备的抗肿瘤甘露葡聚糖(MGA)静脉注射给携带实体MH134肝癌的C3H/He小鼠时,可诱导出一种细胞毒性因子,通过针对L-929成纤维细胞的8小时细胞溶解试验可在肿瘤匀浆中检测到该因子。未经MGA处理时,在肿瘤匀浆中检测不到细胞毒性因子。MGA特异性地在肿瘤组织中诱导细胞毒性因子,在给予MGA后3小时其水平达到最高(24 U/ml):MGA处理后,在正常组织或血清的匀浆中几乎检测不到细胞毒性因子。通过凝胶过滤估计细胞毒性因子的分子大小为70 - 80 kD。它似乎是一种肿瘤坏死因子,因为其活性被抗小鼠肿瘤坏死因子的抗血清所抑制。从这些结果可以得出结论,细胞毒性因子的选择性诱导在MGA的抗肿瘤活性机制中很重要。