Ogura T, Shindo H, Shinzato O, Namba M, Masuno T, Inoue T, Kishimoto S, Yamamura Y
Cancer Immunol Immunother. 1982;13(2):112-7. doi: 10.1007/BF00205310.
The local cellular response induced by intraperitoneal injection of mitomycin C was examined in terms of cell-mediated cytotoxicity for tumor cells. An in vitro cytolysis assay involving 125I-iododeoxyuridine-labeled tumor target cells revealed that treatment of normal ACI/N rats (200 g) with a single intraperitoneal injection of mitomycin C (50, 100, or 200 micrograms) induced tumoricidal macrophages in the peritoneal cavity. The tumoricidal activity was dependent on the dose of mitomycin C injected and it was detectable as early as 1 day after the intraperitoneal injection of mitomycin C. In addition to the increased tumoricidal activity, the functional activities of the peritoneal macrophages were found to be increased with respect both to uptake of 2-deoxy-D-glucose and to phagocytosis of latex beads. Additional experiments excluded the possibility that the tumor cell cytolysis was the result of direct cytotoxicity by mitomycin C that might have been incorporated in the peritoneal macrophages or of nutrient depletion in the medium during the cytolysis assay. Furthermore, endotoxin contamination of the mitomycin C, which might have produced the activated macrophages, was not detected. The mechanism by which mitomycin C injected intraperitoneally induced the tumoricidal macrophages locally remains uncertain; however, it is possible also in clinical situations.
通过肿瘤细胞的细胞介导细胞毒性来检测腹腔注射丝裂霉素C诱导的局部细胞反应。一项涉及125I-碘脱氧尿苷标记肿瘤靶细胞的体外细胞溶解试验显示,对正常ACI/N大鼠(200克)单次腹腔注射丝裂霉素C(50、100或200微克)可诱导腹腔内产生杀肿瘤巨噬细胞。杀肿瘤活性取决于注射的丝裂霉素C剂量,并且在腹腔注射丝裂霉素C后最早1天即可检测到。除了杀肿瘤活性增加外,还发现腹腔巨噬细胞的功能活性在2-脱氧-D-葡萄糖摄取和乳胶珠吞噬方面均有所增加。额外的实验排除了肿瘤细胞溶解是由可能已掺入腹腔巨噬细胞的丝裂霉素C直接细胞毒性或细胞溶解试验期间培养基中营养物质耗尽所致的可能性。此外,未检测到可能产生活化巨噬细胞的丝裂霉素C内毒素污染。腹腔注射丝裂霉素C在局部诱导杀肿瘤巨噬细胞的机制尚不确定;然而,在临床情况下也有可能。