Mironescu S G, Epstein S M, DiPaolo J A
Cancer Res. 1982 Apr;42(4):1274-8.
The cyclic nucleotides, cyclic adenosine 3':5'-monophosphate (cAMP) and cyclic guanosine 3':5'-monophosphate (cGMP) or their dibutyryl and monobrominated derivatives, may either increase or decrease morphological transformation of Syrian hamster embryo cells exposed to N-methyl-N'-nitro-N'-nitrosoguanidine (MNNG). The effect on transformation is primarily a function of the parent cyclic nucleotide and the duration of exposure to the nucleotides. At concentrations of 5 mM or larger for a minimum 24-hr exposure cAMP, cGMP, and their congeners reduced the colony-forming ability of nontransformed Syrian hamster embryo cells not exposed to MNNG; however, cGMP and its derivatives caused less toxicity than cAMP or its analogs. cAMP and its monobrominated and dibutyrylated derivatives decreased the transformation frequency associated with MNNG irrespective of whether the various adenylnucleotides were administered before or after MNNG. The greatest inhibitory effect of MNNG-induced transformation was obtained with N6,O2-dibutyryl cyclic adenosine 3':5'-monophosphate followed in order by 8-bromocyclic adenosine 3':5'-monophosphate and cAMP. At equimolar doses, the dibutyryl and brominated analogs of cGMP but not unsubstituted cGMP enhanced transformation when administered prior to exposure of the Syrian hamster embryo cells to MNNG but reduced the transformation frequency when added after MNNG. The enhancing and inhibitory effects of the guanine cyclic nucleotide-induced alteration of MNNG-associated transformation frequencies were dose and time dependent and occurred in the order N6,O2-dibutyryl cyclic guanosine 3':5'-monophosphate greater than 8-bromocyclic guanosine 3':5-'monophosphate much greater than cGMP. Butyric acid neither diminished nor increased MNNG-induced transformation frequency. The latter suggests that butyrate ions formed by metabolism of the cyclic nucleotide analogs were not a factor in the observed alterations of transformation frequency.
环核苷酸,即环磷酸腺苷(cAMP)和环磷酸鸟苷(cGMP)或它们的二丁酰基和单溴化衍生物,可能会增加或降低暴露于N-甲基-N'-硝基-N'-亚硝基胍(MNNG)的叙利亚仓鼠胚胎细胞的形态转化。对转化的影响主要取决于母体环核苷酸以及核苷酸的暴露持续时间。在浓度为5 mM或更高且至少暴露24小时的情况下,cAMP、cGMP及其同系物降低了未暴露于MNNG的未转化叙利亚仓鼠胚胎细胞的集落形成能力;然而,cGMP及其衍生物的毒性比cAMP或其类似物小。无论各种腺苷核苷酸是在MNNG之前还是之后给药,cAMP及其单溴化和二丁酰化衍生物都降低了与MNNG相关的转化频率。N⁶,O²-二丁酰基环磷酸腺苷对MNNG诱导的转化具有最大的抑制作用,其次是8-溴环磷酸腺苷和cAMP。在等摩尔剂量下,cGMP的二丁酰基和溴化类似物(但不是未取代的cGMP)在叙利亚仓鼠胚胎细胞暴露于MNNG之前给药时会增强转化,但在MNNG之后添加时会降低转化频率。鸟嘌呤环核苷酸诱导的MNNG相关转化频率改变的增强和抑制作用是剂量和时间依赖性的,并且发生的顺序为N⁶,O²-二丁酰基环磷酸鸟苷大于8-溴环磷酸鸟苷远大于cGMP。丁酸既没有降低也没有增加MNNG诱导的转化频率。后者表明,由环核苷酸类似物代谢形成的丁酸根离子不是观察到的转化频率改变的一个因素。