Ohtaki S
Cancer Res. 1978 Dec;38(12):4698-710.
The long latent period required for tumor induction with Simian virus 40 (SV40) in the subcutis of hamsters can be used to investigate whether host factor(s) participate in oncogenesis. Several treatments were applied during this period, and the results were compared with those of the same treatment applied in another series of experiments, homologous SV40 tumor grafting in hamsters. The results obtained were as follows: (a) the latent period for SV40 tumor induction in the female was shorter than that in the male; tumor development was delayed significantly by oophorectomy but was little affected by orchiectomy. Tumor development was markedly delayed in animals of both sexes by estrone given at birth but was accelerated by testosterone given in the adult male; (b) by each of these hormonal modifications, growth of transplanted SV40 tumors was influenced in a different way from that of tumor induction; (c) immunosuppressive treatments, such as thymectomy, administration of antilymphocyte sera, cyclophosphamide, or cortisone acetate delayed and decreased tumor development when applied in the latent period, and the degree or pattern of this effect varied from one procedure to another, depending on the sex and age of the animals; (d) in contrast, tumor growth was markedly accelerated in thymectomized or cortisone-treated hosts irrespective of sex. The different and almost reverse effect of the same procedure in the two phases of tumorigenesis may indicate two discriminating mechanisms operating in the host during these phases. This different effect may be due to virtual absence of any "mature" neoplastic cell in the latent period, except for a few weeks before the appearance of a palpable tumor. These results suggest that the long period of latency may be spent to complete SV40-induced neoplastic conversion of cells, receiving some help by host factors.
猴空泡病毒40(SV40)在仓鼠皮下诱发肿瘤所需的长潜伏期可用于研究宿主因素是否参与肿瘤发生。在此期间进行了几种处理,并将结果与另一系列实验(仓鼠同源SV40肿瘤移植)中相同处理的结果进行了比较。获得的结果如下:(a)雌性中SV40诱发肿瘤的潜伏期比雄性短;卵巢切除显著延迟肿瘤发展,但睾丸切除对其影响很小。出生时给予雌酮会使两性动物的肿瘤发展明显延迟,但成年雄性给予睾酮则会加速肿瘤发展;(b)通过这些激素调节中的每一种,移植的SV40肿瘤的生长受到的影响与肿瘤诱发的影响方式不同;(c)免疫抑制处理,如胸腺切除、给予抗淋巴细胞血清、环磷酰胺或醋酸可的松,在潜伏期应用时会延迟并减少肿瘤发展,这种效应的程度或模式因处理方法而异,取决于动物的性别和年龄;(d)相反,无论性别如何,胸腺切除或用可的松处理的宿主中的肿瘤生长都明显加速。同一程序在肿瘤发生的两个阶段产生的不同且几乎相反的效应可能表明在这些阶段宿主中存在两种不同的作用机制。这种不同的效应可能是由于在潜伏期几乎不存在任何“成熟”的肿瘤细胞,除了在可触及肿瘤出现前的几周。这些结果表明,长潜伏期可能用于完成SV40诱导的细胞肿瘤转化,并得到宿主因素的一些帮助。