Dornish J M, Pettersen E O, Oftebro R
Department of Tissue Culture, Norwegian Radium Hospital, Montebello, Oslo.
Cancer Res. 1988 Feb 15;48(4):938-42.
The cell-inactivating effect induced by cinnamaldehyde in combination with cis-diamminedichloroplatinum(II) (cis-DDP) on human NHIK 3025 cells in culture was investigated. Cell inactivation was measured as a loss in the ability of single cells to give rise to macroscopic colonies following drug treatment. Although 2 h treatment of asynchronous cells with 0.3 mM cinnamaldehyde alone induced little cell inactivation, the drug combination of 0.3 mM cinnamaldehyde and 10 microM cis-DDP resulted in synergistic cell inactivation. Cinnamaldehyde potentiated the cell-inactivating effect of cis-DDP by a dose-modifying factor of 1.8. Drug synergism was found to occur only when cinnamaldehyde and cis-DDP were given in simultaneous combination. Treatment of synchronized cells demonstrated that cinnamaldehyde potentiated the inactivating effect of cis-DDP in all phases of the cell cycle. Cinnamic acid and cinnamyl alcohol were found to have no synergistic or potentiating effect on cell survival following treatment of cells with cis-DDP, thus indicating the importance of an aldehyde moiety for drug synergism.
研究了肉桂醛与顺二氯二氨合铂(II)(顺铂)联合使用对培养的人NHIK 3025细胞的细胞灭活作用。细胞灭活以药物处理后单细胞形成肉眼可见集落的能力丧失来衡量。虽然用0.3 mM肉桂醛单独处理异步细胞2小时几乎不会诱导细胞灭活,但0.3 mM肉桂醛与10 microM顺铂的药物组合导致协同细胞灭活。肉桂醛使顺铂的细胞灭活作用增强,剂量修正因子为1.8。发现仅当肉桂醛和顺铂同时联合使用时才会出现药物协同作用。对同步化细胞的处理表明,肉桂醛在细胞周期的所有阶段均增强了顺铂的灭活作用。在用顺铂处理细胞后,发现肉桂酸和肉桂醇对细胞存活没有协同或增强作用,因此表明醛基部分对药物协同作用的重要性。