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出 处:《环境与健康杂志》2005年第4期261-263,共3页Journal of Environment and Health
摘 要:目的探讨邻苯二甲酸二丁酯(DBP)的拟雌激素活性。方法对雌激素敏感的人乳腺癌MCF-7细胞在RPMI1640培养基中采用开放式单层贴壁培养,开始实验前将细胞用PBS洗涤后改为在无酚红RPMI1640培养基中培养5d,实验设溶剂对照、雌激素阳性对照和邻苯二甲酸二丁酯各剂量组(10-7~10-3mol/L),采用四唑盐(MTT)法、生长曲线、有丝分裂指数和细胞克隆形成试验对MCF-7细胞增殖情况进行分析。结果与溶剂对照组相比,10-5mol/LDBP处理24h就可促进MCF-7细胞增殖,提高增殖指数;随着培养时间延长至96h,其他浓度DBP也表现出促进细胞增殖的效果,且浓度在10-5mol/L时,细胞增殖活性达到最大;在对数生长期,DBP可提高MCF-7细胞的有丝分裂指数;10-5mol/LDBP处理48h就可增强MCF-7细胞形成细胞克隆的能力。结论邻苯二甲酸二丁酯可促进雌激素依赖性乳腺癌MCF-7细胞的增殖,可能具有拟雌激素作用。Objective To determine the estrogenic activity of dibutyl phthalate DBP. Methods The tested compound was dibutyl phthalate. Human estrogen-dependent MCF-7 breast cancer cells were cultured in RPMI 1640 medium containing 10% fetal bovine serum FBS. Five days before the addition of the tested compounds the cells were rinsed by phosphate balanced solution PBS and the medium was substituted with a phenol red-free RPMI 1640 medium containing 5% dextral charcoal-stripped FBS. The respective tested compound was added in fresh medium and the control cells received only the vehicle ethanol. The proliferation of MCF-7 cells was analyzed by the MTT assay growth curves mitotic index and coloning efficiency. Results Compared with the control the proliferation of tested cells treated with DBP like estradiol was markedly enhanced and the activity of the cell proliferation reached the maximum at 10-5 mol/L DBP. During log phase the mitotic index of the test cells treated with DBP and estradiol was significantly increased. The cell coloning efficiency was enhanced which was treated by 10-5 mol/L DBP only for 48 hours. The results showed the time-dependent and dose-dependent model. Conclusion Dibutyl phthalate may enhance the proliferation of human breast cancer MCF-7 cells in vitro that demonstrates an estrogenic activity of dibutyl phthalate.
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