Rivedal E, Sanner T
Cancer Lett. 1985 Aug;28(1):9-17. doi: 10.1016/0304-3835(85)90086-2.
The phosphodiesterase inhibitors caffeine, theophylline, aminophylline and isobutyl-methylxanthine (IBMX) were found to inhibit induction of morphologically transformed hamster embryo cell colonies by sequential exposure to benzo[a]pyrene (BaP) and the tumor promoter TPA. Almost complete inhibition of cell transformation was observed when 50 micrograms/ml theophylline, aminophylline, IBMX, or 200 micrograms/ml caffeine was present together with the tumor promoter. The compounds had no effect on the transformation frequency when present together with the initiator, BaP, in the first exposure period. Substances that stimulate the adenylate cyclase and the addition of exogenous dibutyryl-cAMP had similar inhibitory effects.
磷酸二酯酶抑制剂咖啡因、茶碱、氨茶碱和异丁基甲基黄嘌呤(IBMX)被发现可抑制仓鼠胚胎细胞经连续暴露于苯并[a]芘(BaP)和肿瘤促进剂佛波酯(TPA)后形态转化细胞集落的诱导。当50微克/毫升的茶碱、氨茶碱、IBMX或200微克/毫升的咖啡因与肿瘤促进剂同时存在时,几乎完全抑制了细胞转化。在首次暴露期间,这些化合物与引发剂BaP同时存在时对转化频率没有影响。刺激腺苷酸环化酶的物质以及添加外源性二丁酰环磷腺苷(dibutyryl-cAMP)具有类似的抑制作用。