Gómez-Fabre P M, de Pedro E, Medina M A, Núñez de Castro I, Márquez J
Departamento de Bioquímica y Biología Molecular, Facultad de Ciencias, Universidad de Málaga, Spain.
Cancer Lett. 1997 Feb 26;113(1-2):141-4. doi: 10.1016/s0304-3835(96)04591-0.
The cytotoxic agents chlorpheniramine and dehydrodidemnin B decreased the cell growth of estrogen receptor-negative human breast cancer cells MDA-MB231 and estrogen receptor-positive MCF-7, after 48 h treatment. Both agents reduced ornithine decarboxylase activity, but polyamine levels were increased in MDA-MB231 cells treated with dehydrodidemnin B. MCF-7 cells when treated with dehydrodidemnin B showed significant increases in spermidine and spermine contents. The results suggest that besides other effects, the cytotoxicity of DDB could be explained in part by the over-accumulation of spermidine and spermine.
细胞毒性药物氯苯那敏和脱氢半胱氨酸B在处理48小时后,降低了雌激素受体阴性的人乳腺癌细胞MDA - MB231和雌激素受体阳性的MCF - 7的细胞生长。两种药物都降低了鸟氨酸脱羧酶的活性,但在用脱氢半胱氨酸B处理的MDA - MB231细胞中多胺水平升高。用脱氢半胱氨酸B处理的MCF - 7细胞中,亚精胺和精胺含量显著增加。结果表明,除其他作用外,脱氢半胱氨酸B的细胞毒性部分可由亚精胺和精胺的过度积累来解释。