Sonoda J, Hibasami H, Yamada H, Fujinami S, Nakashima K, Ogihara Y
Department of Orthopedic Surgery, Mie University, Japan.
Anticancer Res. 1995 May-Jun;15(3):907-9.
The antitumor effect of a polyamine biosynthetic pathway inhibitor methylglyoxal bis(cyclopentylamidinohydrazone) (MGBCP) on human osteosarcoma cell lines such as KHOS-240S, MG-63 and G-292 cells, and its effect in combination with anticancer drugs such as methotrexate (MTX), adriamycin (ADM) and 4-hydroperoxyfosfamide (HIFO) have been investigated. The growth of these cultured osteosarcoma cells was inhibited by MGBCP in a dose-dependent manner. Spermidine and spermine levels were dose-dependently depressed in these MGBCP-treated osteosarcoma cells. The antitumor effect of MGBCP was additively potentiated by combined treatment with MTX, ADM and HIFO, respectively.
多胺生物合成途径抑制剂甲基乙二醛双(环戊基脒腙)(MGBCP)对人骨肉瘤细胞系如KHOS - 240S、MG - 63和G - 292细胞的抗肿瘤作用及其与抗癌药物如甲氨蝶呤(MTX)、阿霉素(ADM)和4 - 氢过氧磷酰胺(HIFO)联合使用的效果已被研究。MGBCP以剂量依赖性方式抑制这些培养的骨肉瘤细胞的生长。在这些经MGBCP处理的骨肉瘤细胞中,亚精胺和精胺水平呈剂量依赖性降低。MGBCP分别与MTX、ADM和HIFO联合治疗时,其抗肿瘤作用呈相加增强。