Armuth V, Berenblum I, Adolf W, Opferkuch H J, Schmidt R, Sorg B, Hecker E
J Cancer Res Clin Oncol. 1979 Sep;95(1):19-28. doi: 10.1007/BF00411105.
Phorbol and six structurally related compounds representing the polyfunctional diterpenes of the tigliane, ingenane, and lathyrane types were tested for systemic promoting and leukemogenic activity in SWR mice. For systemic initiation soon after birth, 15 microgram dimethylnitrosamine (DMN) was injected s.c. The diterpenes were administered i.p. either with or without prior systemic initiation with DMN. Systemic promotion was expressed for liver by induction of adenomas with all the diterpenes tested, some of them being more potent than phorbol. The relatively high dose of DMN used as initiator prevented an evaluation of promoting action in relation to lung carcinogenesis. The leukemogenic effect of phorbol in SWR mice was confirmed at three different dose levels. The other diterpenes tested had no significant leukemogenic activity. The leukemogenic action of phorbol was totally inhibited by prior DMN injection. The lack of correlation between promoting action in skin, systemic promoting action in liver and leukemogenic action, among the diterpenes tested, is discussed.
对佛波醇以及六种结构相关的化合物进行了测试,这些化合物代表了大戟烷型、瑞香烷型和山黧豆烷型的多官能二萜,检测它们在SWR小鼠体内的全身促癌和致白血病活性。为在出生后不久进行全身引发,皮下注射15微克二甲基亚硝胺(DMN)。二萜类化合物腹腔注射,无论是否事先用DMN进行全身引发。通过检测的所有二萜类化合物诱导肝脏腺瘤来体现全身促癌作用,其中一些比佛波醇更有效。用作引发剂的相对高剂量DMN妨碍了对其与肺癌发生相关的促癌作用的评估。在三个不同剂量水平上证实了佛波醇对SWR小鼠的致白血病作用。检测的其他二萜类化合物没有显著的致白血病活性。预先注射DMN可完全抑制佛波醇的致白血病作用。讨论了在所检测的二萜类化合物中,皮肤促癌作用、肝脏全身促癌作用和致白血病作用之间缺乏相关性。