Kagawa K, Yamashita T, Tsubura E, Yamamura Y
Cancer Res. 1984 Feb;44(2):665-70.
The antimetastatic activity of Nocardia rubra cell wall skeleton (N-CWS) with or without cyclophosphamide was examined in an experimental model of pulmonary metastasis induced by Lewis lung carcinoma in C57BL/6 mice. Lewis lung carcinoma cells were implanted into the footpads of mice, and the implanted tumors were removed 9 to 10 days later. Pulmonary metastatic nodules began to develop a few days after the implanted tumor was removed. The inhibitory effect of N-CWS was evaluated from the number of pulmonary surface nodules about 3 weeks after tumor implantation. The antimetastatic activity of N-CWS depended upon the dose, time, and route of its injection. Injection of N-CWS i.v. after removal of the implanted tumor caused the greatest inhibition of development of pulmonary metastases. Therapy with N-CWS plus cyclophosphamide prolonged significantly the survival of mice with metastases. The cytotoxic activities of peritoneal macrophages and macrophages in the lung against Lewis lung carcinoma cells were enhanced in mice treated with N-CWS. Injection i.v. of peritoneal macrophages activated with N-CWS inhibited pulmonary metastases. The role of macrophages in inhibition of micrometastasis in the lung is discussed.
在C57BL/6小鼠Lewis肺癌诱导的肺转移实验模型中,研究了有无环磷酰胺情况下红色诺卡氏菌细胞壁骨架(N-CWS)的抗转移活性。将Lewis肺癌细胞接种到小鼠足垫,9至10天后切除接种的肿瘤。切除接种肿瘤几天后开始出现肺转移结节。从肿瘤接种约3周后的肺表面结节数量评估N-CWS的抑制作用。N-CWS的抗转移活性取决于其注射剂量、时间和途径。切除接种肿瘤后静脉注射N-CWS对肺转移的发展抑制作用最大。N-CWS加环磷酰胺治疗显著延长了有转移小鼠的生存期。用N-CWS治疗的小鼠中,腹膜巨噬细胞和肺巨噬细胞对Lewis肺癌细胞的细胞毒活性增强。静脉注射经N-CWS激活的腹膜巨噬细胞可抑制肺转移。讨论了巨噬细胞在抑制肺微转移中的作用。