McCachren S S, Nichols J, Kaufman R E, Niedel J E
Blood. 1986 Aug;68(2):412-6.
The human promyelocytic leukemia cell line HL-60 is induced to differentiate along a myelocytic pathway by dibutyryl cyclic adenosine monophosphate (dbcAMP). Other cAMP analogs are ineffective as inducing agents. The effect of these compounds on expression of c-myc was investigated using a DNA probe for c-myc to detect RNA transcripts. The dose response and time to commitment for reduction in c-myc expression with dbcAMP was similar to the findings for phenotypic changes. Bromo-cyclic AMP and butyrate alone caused no changes in c-myc expression in 24 hours, but demonstrated dramatic synergism together, suggesting that butyrate contributes in part to the effects of dbcAMP. Evidence for mechanisms of action of cAMP other than activation of the cAMP-dependent protein kinase is reviewed.
人早幼粒细胞白血病细胞系HL-60可被二丁酰环磷酸腺苷(dbcAMP)诱导沿髓细胞途径分化。其他环磷酸腺苷类似物作为诱导剂无效。使用c-myc的DNA探针检测RNA转录本,研究了这些化合物对c-myc表达的影响。dbcAMP降低c-myc表达的剂量反应和达到分化的时间与表型变化的结果相似。单独的溴代环磷酸腺苷和丁酸盐在24小时内不会引起c-myc表达的变化,但共同作用时表现出显著的协同作用,表明丁酸盐部分促成了dbcAMP的作用。本文综述了除激活环磷酸腺苷依赖性蛋白激酶外,环磷酸腺苷作用机制的证据。