O'Brien T G, Simsiman R C, Boutwell R K
Cancer Res. 1975 Jul;35(7):1662-70.
A single topical application of 1.0 mg of crotol oil or 17 nmoles of 12-O-tetradecanoyl-phorbol-13-acetate (TPA) resulted in a rapid, transient stimulation of mouse epidermal ornithine decarboxylase activity. The activity reached a peak (230-fold greater than control after TPA) at 4 to 5 hr after croton oil or TPA treatment and returned to control level by 12 hr. The stimulation of S-adenosyl-L-methionine decarboxylase activity was less pronounced, reaching a peak of activity (6- to 7-fold greater than control) at 9 to 12 hr after TPA or croton oil and slowly declining to control level. The stimulation of both enzyme activities was dependent on the dose of TPA applied and correlated well with the promoting ability of these doses on mouse skin. Phorbol, the nonpromoting parent alcohol of TPA, did not affect the enzymes activities. Cycloheximide pretreatment abolished the increase in enzyme activities after TPA application. By measuring the decline of enzyme activity following cycloheximide treatment, enzyme half-lives of 17 and 41 min were obtained for ornithine and S-adenosyl-L-methionine decarboxylase, respectively. 5-Azacytidine pretreatment prevented the stimulation of enzyme activities by TPA, while actinomycin D had no effect. Cordycepin (3'-deoxyadenosine) partially blocked the rise in enzyme activities.
单次局部应用1.0毫克巴豆油或17纳摩尔的12 - O - 十四烷酰佛波醇 - 13 - 乙酸酯(TPA)可导致小鼠表皮鸟氨酸脱羧酶活性迅速、短暂地升高。在巴豆油或TPA处理后4至5小时,该活性达到峰值(TPA处理后比对照高230倍),并在12小时时恢复到对照水平。S - 腺苷 - L - 甲硫氨酸脱羧酶活性的升高不太明显,在TPA或巴豆油处理后9至12小时达到活性峰值(比对照高6至7倍),然后缓慢下降至对照水平。两种酶活性的升高均取决于所应用的TPA剂量,并且与这些剂量对小鼠皮肤的促癌能力密切相关。佛波醇是TPA的非促癌母体醇,不影响酶活性。环己酰亚胺预处理消除了TPA应用后酶活性的增加。通过测量环己酰亚胺处理后酶活性的下降,分别得到鸟氨酸脱羧酶和S - 腺苷 - L - 甲硫氨酸脱羧酶的酶半衰期为17分钟和41分钟。5 - 氮杂胞苷预处理可防止TPA对酶活性的刺激,而放线菌素D则无影响。虫草素(3'-脱氧腺苷)部分阻断了酶活性的升高。