Bhisey R A, Ramchandani A G, Sirsat S M
Carcinogenesis. 1984 Feb;5(2):135-41. doi: 10.1093/carcin/5.2.135-a.
The effects of a single application of 1.8 nmol 12-O-tetradecanoylphorbol-13-acetate (TPA) on precursor incorporation into RNA, DNA and protein in the epidermis, dermis and subcutis from 3-methylcholanthrene (MCA) injected precancerous mouse skin were studied at various time points between 3 and 96 h. In the precancerous tissues, the rates of incorporation of [3H]uridine into RNA did not alter appreciably from those in the control tissues; while the rates of [3H]methylthymidine incorporation into DNA were elevated with peaks appearing between 6 and 12 h, at 24 h and at 72 h in epidermis, dermis and subcutis. The rate of incorporation of [14C]leucine into protein was markedly elevated in all the three tissues which showed 3-4 sharp peaks. The maximum stimulation ranged between 14 and 20 times that of the control. A single application of TPA to the precancerous mouse skin induced early stimulation of precursor incorporation into all the three macromolecules in epidermis, dermis and subcutis. The increased stimulation was maintained for 36-72 h. The patterns of incorporation of [3H]methylthymidine into DNA gave rise to 2-3 peaks of elevated uptake in each tissue up to 36-48 h. A lowered rate of DNA synthesis between 48 and 60 h was followed by a peak at 72 h. In each group, epidermal mitotic activity correlated well with spurts of precursor incorporation into cellular DNA. The observations indicate that TPA recruits more cells into the DNA synthetic phase and accelerates selective growth of preneoplastic cells during tumor progression.
研究了单次应用1.8 nmol 12 - O - 十四烷酰佛波醇 - 13 - 乙酸酯(TPA)对注射3 - 甲基胆蒽(MCA)的癌前小鼠皮肤的表皮、真皮和皮下组织中前体掺入RNA、DNA和蛋白质的影响,观察时间点为3至96小时之间的不同时段。在癌前组织中,[3H]尿苷掺入RNA的速率与对照组织相比无明显变化;而[3H]甲基胸苷掺入DNA的速率升高,在表皮、真皮和皮下组织中,峰值分别出现在6至12小时、24小时和72小时。[14C]亮氨酸掺入蛋白质的速率在所有三个组织中均显著升高,出现3 - 4个尖峰。最大刺激程度为对照的14至20倍。单次给癌前小鼠皮肤应用TPA可早期刺激表皮、真皮和皮下组织中前体掺入所有三种大分子。增强的刺激持续36至72小时。[3H]甲基胸苷掺入DNA的模式在每个组织中直至36至48小时产生2至3个摄取升高的峰。48至60小时DNA合成速率降低,随后在72小时出现一个峰。在每组中,表皮有丝分裂活性与前体掺入细胞DNA的激增密切相关。这些观察结果表明,TPA在肿瘤进展过程中使更多细胞进入DNA合成期,并加速癌前细胞的选择性生长。