Raikow R B, OKunewick J P, Buffo M J, Kociban D L
Cancer Res. 1985 Feb;45(2):555-7.
The influence of cyclophosphamide (CY) on Friend virus leukemogenesis was studied in SJL/J, C57BL/10J, and C57BL/10J X SJL/J F1 (hereafter called B10SJF1) mice. All three differ in their susceptibility to the viral oncogenic effect. Immunosuppressive doses of CY, which by themselves produced no cancer, were followed 2 days later by injection of Friend leukemia virus. The virus doses were the same as used previously. Although in other experiments preinjection of various chemical carcinogens augmented leukemogenesis by Friend leukemia virus in SJL/J mice, in the present study, pretreatment by CY had no such effect. In contrast, CY increased Friend erythroleukemia incidence from 15 to 100% in B10SJF1 mice and from 0 to 85% in C57BL/10J mice. The disease in C57BL/10J mice had a 190-day incubation period, which is approximately 5 times that in the SJL/J and B10SJF1 mice. During this latent period, the C57BL/10J mice harbored infectious Friend leukemia virus in their plasma.
研究了环磷酰胺(CY)对SJL/J、C57BL/10J和C57BL/10J×SJL/J F1(以下简称B10SJF1)小鼠中Friend病毒白血病发生的影响。这三种小鼠对病毒致癌作用的易感性各不相同。给予免疫抑制剂量的CY(其本身不会引发癌症),两天后注射Friend白血病病毒。病毒剂量与之前使用的相同。尽管在其他实验中,预先注射各种化学致癌物会增强SJL/J小鼠中Friend白血病病毒的白血病发生,但在本研究中,CY预处理没有这种效果。相反,CY使B10SJF1小鼠中Friend红白血病的发病率从15%提高到100%,使C57BL/10J小鼠中Friend红白血病的发病率从0提高到85%。C57BL/10J小鼠的疾病潜伏期为190天,约为SJL/J和B10SJF1小鼠潜伏期的5倍。在这个潜伏期内,C57BL/10J小鼠的血浆中携带传染性Friend白血病病毒。