Carmel R J, Brown J M
Cancer Res. 1977 Jan;37(1):145-51.
A study was made of the effect of various cytotoxic drugs on the ability of i.v.-injected KHT sarcoma cells to form lung colonies in syngeneic C3H mice. Some enhancement of the number of lung colonies following an i.v. injection was seen following pretreatment of the mice with actinomycin D and mithramycin, while pretreatment with vinblastine, bleomycin, methotrexate, cytosine arabinoside, or 5-fluorouracil had little or no effect on lung colony formation. Pretreatment of the mice with cyclophosphamide, however, greatly increased lung colony formation (by a factor of approximately 100). This enhancement in lung colony formation was maximal when the drug was given 24 hr prio to the injection of tumor cells, but was seen as early as 2 hr and persisted as long as 8 weeks prior to the tumor cell injection. The degree of enhancement of lung colony formation was related to the dose of cyclophosphamide and was present in weaning as well as adult mice. This enhancement was not significantly reversed by anticoagulation with either aspirin or warfarin. Immunosuppression by whole-body irradiation did not affect the number of lung colonies seen in cyclophosphamide-treated mice. The mechanism by which cyclophosphamide enhances metastatic tumor growth within the lung is not known. The major effect, however, does not appear to be mediated either by specific immunological or clotting factors.
研究了各种细胞毒性药物对静脉注射的KHT肉瘤细胞在同基因C3H小鼠肺部形成集落能力的影响。在用放线菌素D和光辉霉素预处理小鼠后,静脉注射后肺部集落数量有所增加,而用长春碱、博来霉素、甲氨蝶呤、阿糖胞苷或5-氟尿嘧啶预处理对肺部集落形成几乎没有影响。然而,用环磷酰胺预处理小鼠后,肺部集落形成大大增加(约增加100倍)。当在注射肿瘤细胞前24小时给予该药物时,肺部集落形成的增强最为明显,但早在注射肿瘤细胞前2小时就可见到,并且在注射肿瘤细胞前长达8周持续存在。肺部集落形成的增强程度与环磷酰胺的剂量有关,在断奶小鼠和成年小鼠中均存在。用阿司匹林或华法林进行抗凝并不能显著逆转这种增强作用。全身照射引起的免疫抑制并不影响环磷酰胺处理小鼠肺部的集落数量。环磷酰胺增强肺部转移性肿瘤生长的机制尚不清楚。然而,主要作用似乎不是由特定的免疫或凝血因子介导的。