Kunimoto T, Baba H, Nitta K
Chemotherapy Division, National Cancer Center Research Institute, Tokyo, Japan.
Hum Cell. 1990 Jun;3(2):124-30.
A potent tumor-regressing activity was found in the serum of mice with S180 tumor undergoing rapid regression caused by antitumor polysaccharides. Beta (1-3) glucan including CM-TAK and lentinan and mannoglucan MGA induced such activity. It causes a rapid decrease in the number of tumor cells accompanied with a marked increase in neutrophiles in solid tumors. The entity of the activity was named as tumor-regressing factor (TRF) and was partially purified revealing a proteinaceous nature with an approximate molecular weight of 250,000. The factor was induced in a serum of tumor-bearing mice in various host-tumor combinations after the tumor growth had been established but only weakly in normal mice. The sensitivity of tumors to the factor was also dependent on the stage of tumor growth. The serum of normal mice or tumor-bearing mice without polysaccharide treatment exhibited similar activity as TRF after definite chromatographic step. The chromatographic behavior of the revealed activity was closely similar to that of the induced factor. It was postulated that a TRF-like activity exists in normal serum in a inactivated form being bound by antagonist(s) and the appropriate chromatography might remove the antagonist resulting in the active form of the factor. The concept was confirmed by reconstituting the chromatographic fractions, the revealed activity was again obscured after mixing with a certain fraction.
在由抗肿瘤多糖导致S180肿瘤快速消退的小鼠血清中发现了一种强大的肿瘤消退活性。包括CM-TAK和香菇多糖在内的β(1-3)葡聚糖以及甘露葡聚糖MGA可诱导这种活性。它会导致肿瘤细胞数量迅速减少,同时实体瘤中的嗜中性粒细胞显著增加。这种活性物质被命名为肿瘤消退因子(TRF),并经过部分纯化,显示出蛋白质性质,分子量约为250,000。该因子在肿瘤生长确立后,在各种宿主-肿瘤组合的荷瘤小鼠血清中被诱导产生,但在正常小鼠中诱导程度较弱。肿瘤对该因子的敏感性也取决于肿瘤生长阶段。经过特定色谱步骤后,正常小鼠或未接受多糖治疗的荷瘤小鼠血清表现出与TRF相似的活性。所揭示活性的色谱行为与诱导因子的色谱行为非常相似。据推测,正常血清中存在一种以失活形式存在的TRF样活性,它与拮抗剂结合,适当的色谱法可能会去除拮抗剂,从而产生该因子的活性形式。通过重组色谱馏分证实了这一概念,与某一组分混合后,所揭示的活性再次消失。