James K, Cullen R T, Milne I, Norval M
Br J Cancer. 1978 Feb;37(2):269-81. doi: 10.1038/bjc.1978.36.
The injection (s.c. or i.p.) of 10(6) live or lethally irradiated methylcholanthrene-induced fibrosarcoma cells into CBA/Ca mice one or 2 days before i.v. challenge with the same tumour inhibited the formation of artificial lung tumour metastases. In addition, it also frequently enhanced the cytostatic effect of peritoneal exudate cells on monolayers of the same tumour. The effects on lung tumour metastasis were not noted if X-irradiated tumour was injected i.v., or if s.c. administration was delayed until one day after i.v. challenge. Similar effects on tumour growth were also observed in C3Hf/Bu mice and (CBA/Ca x A/HeJ) F1 hybrids which were pretreated (s.c.) with tumour shortly before i.v. challenge with the same tumour. Further studies in CBA/Ca mice suggested that the protective effect was tumour-specific, for the growth of i.v. injected tumour was not significantly inhibited by pretreatement with a number of other MC-induced or spontaneous tumours from the same and different strains.
在静脉注射相同肿瘤细胞前1天或2天,给CBA/Ca小鼠皮下或腹腔注射10(6)个活的或经致死剂量照射的甲基胆蒽诱导的纤维肉瘤细胞,可抑制人工肺肿瘤转移灶的形成。此外,它还常常增强腹腔渗出细胞对同一肿瘤单层细胞的细胞抑制作用。如果静脉注射经X射线照射的肿瘤细胞,或者皮下给药延迟至静脉注射攻击后1天,则未观察到对肺肿瘤转移的影响。在C3Hf/Bu小鼠和(CBA/Ca×A/HeJ)F1杂种小鼠中,在静脉注射相同肿瘤细胞前不久经皮下用肿瘤进行预处理,也观察到对肿瘤生长的类似影响。对CBA/Ca小鼠的进一步研究表明,这种保护作用具有肿瘤特异性,因为用来自相同和不同品系的许多其他甲基胆蒽诱导的或自发的肿瘤进行预处理,并未显著抑制静脉注射肿瘤的生长。