Huang F L, Hasuma T, Cho-Chung Y S
Cancer Res. 1984 Apr;44(4):1595-9.
Carcinogenic doses of 7,12-dimethylbenz(alpha)anthracene (DMBA) failed to induce mammary carcinoma in the rats that have received N6,O2'-dibutyryl cyclic adenosine 3',5'-monophosphate (DBcAMP) (Cancer Res., 43: 2736, 1983). We now report that the anticarcinogenic effect of DBcAMP correlates with its effect on DNA binding of the carcinogen and on gene expression. Cultured mammary epithelial cells in exponential phase of growth were used to determine the effect of DBcAMP on DMBA binding to DNA. DBcAMP inhibited the DMBA binding in carcinogen-susceptible mammary cells of 50-day-old rats, but it had no effect on the binding in the DMBA-resistant mammary cells of 35- and 110-day-old rats. The inhibitory effect of DBcAMP was appreciable at the concentration of 10(-7) M, one tenth the concentration of [3H]DMBA. DBcAMP at 10(-6) M concentration exhibited the maximal inhibition of DMBA binding; i.e., binding in DMBA-susceptible mammary cells was reduced to the level of binding observed in DMBA-resistant mammary cells. Polyadenylate-containing RNAs isolated from mammary glands of DMBA-susceptible rats (50-day-old) yielded translation products in vitro which bear a greater resemblance to translation products of growing DMBA-induced tumors than they do to products of messenger RNAs from regressing tumors or DMBA-resistant mammary glands of 110-day-old rats. DBcAMP administered to the susceptible rats resulted in changes in the translation products of the mammary glands; the translation products of the glands became similar to those of DMBA-resistant mammary glands or regressing tumors. DMBA feeding 1 day after DBcAMP treatment could not reverse this effect of DBcAMP. These data suggest that the role of cyclic adenosine 3',5'-monophosphate at the genomic level is responsible for the anticarcinogenesis of mammary cells.
致癌剂量的7,12-二甲基苯并(α)蒽(DMBA)未能在接受N6,O2'-二丁酰环腺苷3',5'-单磷酸(DBcAMP)的大鼠中诱发乳腺癌(《癌症研究》,43: 2736, 1983)。我们现在报告,DBcAMP的抗癌作用与其对致癌物DNA结合及基因表达的影响相关。处于指数生长期的培养乳腺上皮细胞被用于确定DBcAMP对DMBA与DNA结合的影响。DBcAMP抑制了50日龄大鼠致癌物敏感乳腺细胞中的DMBA结合,但对35日龄和110日龄大鼠的DMBA抗性乳腺细胞中的结合没有影响。DBcAMP在10(-7) M浓度时具有明显的抑制作用,该浓度是[3H]DMBA浓度的十分之一。10(-6) M浓度的DBcAMP对DMBA结合表现出最大抑制作用;即致癌物敏感乳腺细胞中的结合减少到了在DMBA抗性乳腺细胞中观察到的结合水平。从DMBA敏感大鼠(50日龄)乳腺中分离出的含聚腺苷酸的RNA在体外产生的翻译产物,与正在生长的DMBA诱导肿瘤的翻译产物的相似性,高于与消退肿瘤或110日龄大鼠的DMBA抗性乳腺的信使RNA产物的相似性。给敏感大鼠施用DBcAMP导致乳腺的翻译产物发生变化;乳腺的翻译产物变得与DMBA抗性乳腺或消退肿瘤的翻译产物相似。在DBcAMP处理1天后喂食DMBA无法逆转DBcAMP的这种作用。这些数据表明,环腺苷3',5'-单磷酸在基因组水平的作用是乳腺细胞抗癌发生的原因。