He Y, Shimogori T, Kashiwagi K, Shirahata A, Igarashi K
Faculty of Pharmaceutical Sciences, Chiba University.
J Biochem. 1995 Apr;117(4):824-9. doi: 10.1093/oxfordjournals.jbchem.a124782.
The inhibitory effect on cell growth of a combination of alpha-difluoromethylornithine (DFMO) and an inhibitor of aminopropyl transferase was examined. N-(3-aminopropyl)cyclohexylamine (APCHA) and trans-4-methylcyclohexylamine (4MCHA) were used as inhibitors of spermine and spermidine synthases, respectively. Combination of DFMO and APCHA showed strong inhibitory effects on the growth of FM3A cultured cells and P388 leukemia cells in mice, compared with DFMO alone. The prolongation of survival time of P388 leukemia-bearing mice by DFMO (1,500 mg/kg) was 1.12-fold, while that by DFMO (1,500 mg/kg) plus APCHA (25 mg/kg) was 1.30-fold. The prolongation of survival time nearly paralleled the decrease of P388 leukemia cells in mice. However, the antiproliferative effect of DFMO was not strengthened by 4MCHA in the above two experimental systems. In the FM3A cell culture system, both putrescine and spermidine contents were decreased by DFMO, but spermine content did not decrease significantly. When APCHA was added to the medium with DFMO, spermine content was decreased greatly but a compensatory increase in spermidine was observed. Spermidine content in P388 leukemia cells was also decreased by DFMO, the increase in spermine was suppressed but a compensatory increase in spermidine was observed. Nevertheless, the spermidine content remained significantly low compared with the value in non-treated P388 leukemia cells. Thus, the results indicate that the antiproliferative effect of DFMO was strengthened by APCHA due to the decrease in spermine content, and that the decrease in total amount of spermidine and spermine, especially the decrease in spermine, is necessary for inhibition of cell growth.
研究了α-二氟甲基鸟氨酸(DFMO)与氨基丙基转移酶抑制剂联合使用对细胞生长的抑制作用。分别使用N-(3-氨基丙基)环己胺(APCHA)和反式-4-甲基环己胺(4MCHA)作为精胺和亚精胺合酶的抑制剂。与单独使用DFMO相比,DFMO与APCHA联合使用对小鼠FM3A培养细胞和P388白血病细胞的生长具有强烈的抑制作用。DFMO(1500mg/kg)使荷P388白血病小鼠的存活时间延长1.12倍,而DFMO(1500mg/kg)加APCHA(25mg/kg)使存活时间延长1.30倍。存活时间的延长与小鼠体内P388白血病细胞数量的减少几乎平行。然而,在上述两个实验系统中,4MCHA并未增强DFMO的抗增殖作用。在FM3A细胞培养系统中,DFMO使腐胺和亚精胺含量均降低,但精胺含量没有显著降低。当在含有DFMO的培养基中加入APCHA时,精胺含量大幅降低,但观察到亚精胺有代偿性增加。DFMO也使P388白血病细胞中的亚精胺含量降低,精胺的增加受到抑制,但观察到亚精胺有代偿性增加。然而,与未处理的P388白血病细胞相比,亚精胺含量仍显著较低。因此,结果表明,由于精胺含量降低,APCHA增强了DFMO的抗增殖作用,并且亚精胺和精胺总量的减少,尤其是精胺的减少,是抑制细胞生长所必需的。