Bergamo A, Cocchietto M, Capozzi I, Mestroni G, Alessio E, Sava G
Fondazione CD Callerio, Institutes of Biological Research, Trieste, Italy.
Anticancer Drugs. 1996 Aug;7(6):697-702. doi: 10.1097/00001813-199608000-00011.
Treatment of MCa mammary carcinoma metastases by i.p. administration of a total dose of 450 mg/kg Na[trans-RuCl4(DMSO)lm], after successful surgical removal of primary tumor mass, causes a significant prolongation of the host's life-time expectancy. This effect, related to lung metastasis inhibition, seems not attributable to a direct inhibition of tumor cells since antimetastatic effects can be achieved also when drug treatment occurs before tumor cell injection into the host. Also, the activity of Na[trans-RuCl4(DMSO)lm] seems independent of its concentration in tumor cells. Rather it must be stressed that the fate of this compound in the blood, following i.v. administration, is fast and only a very low percent of the total dose reaches the tumor target in the lungs. These data emphasize the possibility that Na[trans-RuCl4(DMSO)lm] increases the resistance of the host against metastasis formation, possibly by the already shown mechanism of potentiation of the extracellular matrix and reduction of blood stream invasion by tumor cells.
在成功手术切除原发性肿瘤块后,通过腹腔注射总剂量为450 mg/kg的Na[trans-RuCl4(DMSO)lm]来治疗MCa乳腺癌转移,可显著延长宿主的预期寿命。这种与肺转移抑制相关的效应似乎并非归因于对肿瘤细胞的直接抑制,因为在将肿瘤细胞注入宿主之前进行药物治疗时也能实现抗转移效果。此外,Na[trans-RuCl4(DMSO)lm]的活性似乎与其在肿瘤细胞中的浓度无关。必须强调的是,静脉注射后该化合物在血液中的命运很快,总剂量中只有非常低的百分比到达肺部的肿瘤靶点。这些数据强调了Na[trans-RuCl4(DMSO)lm]可能通过已显示的增强细胞外基质和减少肿瘤细胞对血流侵袭的机制来增加宿主对转移形成的抵抗力。