Takahashi Y, Urade M, Kishimoto H, Arimoto T, Yanagisawa T, Yoshioka W
Dept. of Dentistry and Oral Surgery, Hyogo College of Medicine.
Gan To Kagaku Ryoho. 1995 Jun;22(7):883-7.
Combined effect of bleomycin (BLM) and N-solanyl-N, N'-bis (3, 4-di-methoxy-benzyl)-ethylenediamine (SDB-ethylenediamine), a synthetic isoprenoid was studied on 3 oral squamous carcinoma cell lines (SCCTF, SCCKN, SCCRY) and clonal cell lines from SCCRY in vitro and on transplantable nude mouse tumors. The cytotoxicity of SDB-ethylenediamine varied among those cell lines in vitro. SDB-ethylenediamine potentiated more than 2-fold the cytotoxic effect of BLM in 6 cell lines, but no distinct correlation was found between cytotoxicity of SDB-ethylenediamine and potentiation by BLM. Compared with verapamil, the cytotoxic effect of BLM was potentiated 3.9-fold by SDB-ethylenediamine in SCCTF. The growth of the transplantable nude mouse tumors (SCCRY and SCCTF) was strongly suppressed when BLM was combined with SDB-ethylenediamine. Correlation between BLM resistance and potentiation of BLM by SDB-ethylenediamine was not observed in this experiment.
研究了博来霉素(BLM)与合成类异戊二烯N-茄呢基-N,N'-双(3,4-二甲氧基苄基)乙二胺(SDB-乙二胺)对3种口腔鳞状癌细胞系(SCCTF、SCCKN、SCCRY)以及SCCRY的克隆细胞系的体外联合作用,以及对可移植裸鼠肿瘤的作用。SDB-乙二胺在这些细胞系中的体外细胞毒性各不相同。SDB-乙二胺在6种细胞系中使BLM的细胞毒性增强了2倍以上,但SDB-乙二胺的细胞毒性与BLM的增效作用之间未发现明显相关性。与维拉帕米相比,在SCCTF中,SDB-乙二胺使BLM的细胞毒性增强了3.9倍。当BLM与SDB-乙二胺联合使用时,可移植裸鼠肿瘤(SCCRY和SCCTF)的生长受到强烈抑制。在本实验中未观察到BLM耐药性与SDB-乙二胺对BLM的增效作用之间的相关性。