Saydjari R, Townsend C M, Barranco S C, Thompson J C
Life Sci. 1987 Jan 26;40(4):359-66. doi: 10.1016/0024-3205(87)90137-8.
The growth and survival of mouse (MC-26) colon carcinoma in vitro and in vivo are significantly reduced by inhibitors of polyamine biosynthesis. alpha-Difluoromethylornithine (DFMO), is a specific and irreversible inhibitor of ornithine decarboxylase (ODC); the rate-limiting enzyme in polyamine biosynthesis. DFMO treatment inhibits the growth of MC-26 colon cancer cells and decreases MC-26 cell survival both in vitro and in vivo. In the present study, we examined the effects of cyclosporine (CsA) on growth, survival, and polyamine levels in MC-26 colon cancer in vitro. CsA had inhibitory effects on MC-26 colon cancer growth which were similar to DFMO; these effects were blocked by the addition of the polyamine, putrescine. The combination of CsA (8.3 X 10(-4) mM) and DFMO (0.5 mM or 1.0 mM) inhibited MC-26 cell survival to a greater extent than either agent alone. These results suggest that CsA given in combination with other agents which inhibit polyamine synthesis may be useful for the treatment of colon cancer.
多胺生物合成抑制剂可显著降低小鼠(MC - 26)结肠癌在体外和体内的生长及存活率。α-二氟甲基鸟氨酸(DFMO)是鸟氨酸脱羧酶(ODC)的一种特异性不可逆抑制剂;ODC是多胺生物合成中的限速酶。DFMO处理可抑制MC - 26结肠癌细胞的生长,并降低其在体外和体内的存活率。在本研究中,我们检测了环孢素(CsA)对体外培养的MC - 26结肠癌生长、存活及多胺水平的影响。CsA对MC - 26结肠癌生长具有抑制作用,这与DFMO相似;添加多胺腐胺可阻断这些作用。CsA(8.3×10⁻⁴ mM)与DFMO(0.5 mM或1.0 mM)联合使用比单独使用任一药物更能抑制MC - 26细胞存活。这些结果表明,CsA与其他抑制多胺合成的药物联合使用可能对结肠癌治疗有用。