Chu E, Koeller D M, Johnston P G, Zinn S, Allegra C J
NCI-Navy Medical Oncology Branch, Bethesda, Maryland 20889.
Mol Pharmacol. 1993 Apr;43(4):527-33.
The effects of fluorouracil (5-FU) and interferon-gamma (IFN-gamma) on the regulation of thymidylate synthase (TS) gene expression were investigated in the human colon cancer H630 cell line. By Western immunoblot analysis, TS protein levels in H630 cells were increased 3-, 5.5-, 5-, and 2.5-fold after 8-, 16-, 24-, and 36-hr exposure to 1 microM 5-FU, respectively. When H630 cells were exposed to varying concentrations of 5-FU (0.3-10 microM) for 24 hr, increases in TS protein up to 5.5-fold were observed. A 24-hr exposure to 1 microM 5-FU resulted in a 4.5-fold increase in the level of TS protein, whereas in 5-FU/IFN-gamma-treated cells TS protein was increased by only 1.8-fold, compared with control cells. IFN-gamma treatment alone did not affect TS protein levels, relative to control. Northern blot analysis revealed no changes in TS mRNA levels when H630 cells were exposed either to 1 microM 5-FU for 8-36 hr, to varying concentrations of 5-FU (0.3-10 microM) for 24 hr, or to the combination of 5-FU and IFN-gamma. Pulse-labeling studies with [35S]methionine demonstrated a 3.5-fold increase in net synthesis of TS in cells treated with 1 microM 5-FU, whereas the level of newly synthesized TS increased only 1.5-fold in cells treated with 5-FU/IFN-gamma, compared with control cells. Pulse-chase studies revealed that the half-lives of TS protein in control and 5-FU-treated cells were equivalent. These findings demonstrate that the increase in TS protein after 5-FU exposure and the subsequent inhibitory effect of IFN-gamma on TS protein expression are both regulated at the post-transcriptional level.
在人结肠癌H630细胞系中研究了氟尿嘧啶(5-FU)和γ-干扰素(IFN-γ)对胸苷酸合成酶(TS)基因表达调控的影响。通过蛋白质免疫印迹分析,H630细胞在分别暴露于1μM 5-FU 8、16、24和36小时后,TS蛋白水平分别增加了3倍、5.5倍、5倍和2.5倍。当H630细胞暴露于不同浓度的5-FU(0.3 - 10μM)24小时时,观察到TS蛋白增加高达5.5倍。暴露于1μM 5-FU 24小时导致TS蛋白水平增加4.5倍,而与对照细胞相比,在5-FU/IFN-γ处理的细胞中TS蛋白仅增加1.8倍。相对于对照,单独的IFN-γ处理不影响TS蛋白水平。Northern印迹分析显示,当H630细胞暴露于1μM 5-FU 8 - 36小时、不同浓度的5-FU(0.3 - 10μM)24小时或5-FU与IFN-γ的组合时,TS mRNA水平没有变化。用[35S]甲硫氨酸进行的脉冲标记研究表明,用1μM 5-FU处理的细胞中TS的净合成增加了3.5倍,而与对照细胞相比,用5-FU/IFN-γ处理的细胞中新合成的TS水平仅增加了1.5倍。脉冲追踪研究表明,对照细胞和5-FU处理细胞中TS蛋白的半衰期相当。这些发现表明,5-FU暴露后TS蛋白的增加以及IFN-γ随后对TS蛋白表达的抑制作用均在转录后水平受到调控。