Abe S, Kubota T, Otani Y, Furukawa T, Watanabe M, Kumai K, Kitajima M
Department of Surgery, School of Medicine, Keio University, Shinjuku-ku, Tokyo 160-8582, Japan.
Jpn J Cancer Res. 2000 Nov;91(11):1192-8. doi: 10.1111/j.1349-7006.2000.tb00904.x.
UCN-01 (7-hydroxystaurosporine) is a newly developed cell cycle inhibitor known to have several modes of action, including inhibition of cyclin-dependent kinase, induction of p21 and suppression of pRb phosphorylation. In order to test a combination therapy of UCN-01 and 5-fluorouracil (5-FU), growth inhibition of CRL 1420 (MIA PaCa-2; undifferentiated pancreatic carcinoma) by four different treatments was measured using the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl-2H-tetrazolium bromide (MTT) assay. The treatments used were UCN-01 alone, 5-FU alone, 5-FU followed by UCN-01 (5-FU/UCN-01) and UCN-01 followed by 5-FU (UCN-01/5-FU). We also assessed changes in thymidylate synthetase (TS) mRNA levels, TS activity, and 5-FU incorporation by RNA (F-RNA) for each treatment. Although treatment with UCN-01 alone, 5-FU alone, and 5-FU/UCN-01 inhibited CRL 1420 growth in a concentration-dependent manner, treatment with UCN-01/5-FU inhibited the growth of CRL 1420 synergistically at less than 1 microg/ml drug concentration. The down-regulation of TS mRNA by UCN-01 resulted in stable total TS and decreased free TS, and UCN-01/ 5-FU resulted in enhanced thymidylate synthetase inhibition rate (TSIR) compared to UCN-01 alone and 5-FU/UCN-01. This increased TSIR due to UCN-01 pretreatment was accompanied by elevated F-RNA concentrations in the UCN-01/5-FU treatment. The suppression of TS mRNA and TS activity by UCN-01 may lead to higher sensitivity of tumor cells to 5-FU and may explain the synergistic antitumor effect of UCN-01/5-FU. In conclusion, low concentrations of UCN-01 (from 0.01 to 1 microg/ml) may be clinically useful, affording low cytotoxicity of UCN-01, while enhancing the antitumor effect of 5-FU.
UCN - 01(7 - 羟基星孢菌素)是一种新开发的细胞周期抑制剂,已知具有多种作用模式,包括抑制细胞周期蛋白依赖性激酶、诱导p21以及抑制pRb磷酸化。为了测试UCN - 01与5 - 氟尿嘧啶(5 - FU)的联合治疗效果,使用3 -(4,5 - 二甲基噻唑 - 2 - 基)- 2,5 - 二苯基 - 2H - 四氮唑溴盐(MTT)法测定了四种不同处理对CRL 1420(MIA PaCa - 2;未分化胰腺癌)细胞生长的抑制作用。所采用的处理方式分别为单独使用UCN - 01、单独使用5 - FU、5 - FU后使用UCN - 01(5 - FU/UCN - 01)以及UCN - 01后使用5 - FU(UCN - 01/5 - FU)。我们还评估了每种处理方式下胸苷酸合成酶(TS)mRNA水平、TS活性以及5 - FU掺入RNA(F - RNA)的变化。尽管单独使用UCN - 01、单独使用5 - FU以及5 - FU/UCN - 01均以浓度依赖性方式抑制CRL 1420细胞生长,但在药物浓度低于1微克/毫升时,UCN - 01/5 - FU联合处理对CRL 1420细胞生长具有协同抑制作用。UCN - 01导致TS mRNA下调,使总TS稳定且游离TS减少,与单独使用UCN - 01和5 - FU/UCN - 01相比,UCN - 01/5 - FU联合处理导致胸苷酸合成酶抑制率(TSIR)提高。UCN - 01预处理导致TSIR升高,同时UCN - 01/5 - FU处理中的F - RNA浓度也升高。UCN - 01对TS mRNA和TS活性的抑制可能导致肿瘤细胞对5 - FU的敏感性增加,这可能解释了UCN - 01/5 - FU联合治疗的协同抗肿瘤作用。总之,低浓度的UCN - 01(0.01至1微克/毫升)可能在临床上有用,既能降低UCN - 01的细胞毒性,又能增强5 - FU的抗肿瘤效果。