牛油果挥发油对MCF7人乳腺癌细胞系及雌性wistar大鼠的化学成分及抗增殖作用

S. Bagheri, Davood Javidmehr, M. Ghaffari, Ehsan Ghoderti-Shatori
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引用次数: 4

摘要

背景:乳腺癌是女性癌症相关死亡的主要原因,其发病率在世界范围内呈上升趋势。在体内和体外研究中,asafetida均显示出良好的抗乳腺癌活性。材料与方法:为评价荷叶花精油(EOA)的细胞毒作用,将高侵袭性人乳腺癌细胞系MCF7细胞暴露于不同浓度的EOA(2、4、6、8和10 μl/ml)中不同时间(24、48和72 h),采用3-(4,5-二甲基噻唑-2-基)-2,5-二苯基溴化四唑(MTT)法分析细胞活力。实验采用0.1、1、10、100 μl/kg的剂量给雌性Wistar大鼠口服EOA油28 d,测定其体内毒性。实验结束后,进行血液学和血清生化指标评估,并与未治疗组进行比较。结果:MTT实验结果显示,EOA显著降低MCF7细胞活力,且呈时间和浓度依赖性,表明EOA对乳腺癌细胞具有较强的细胞毒作用。在慢性毒性研究中,雌性Wistar大鼠在任何给药剂量下,血液学和生化参数均未发生变化。结论:EOA对乳腺癌细胞具有细胞毒作用,无一般毒性,是一种很有前景的乳腺癌辅助治疗药物。
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Chemical compositions and antiproliferative effect of essential oil of asafoetida on MCF7 human breast cancer cell line and female wistar rats
Background: Breast cancer is a leading cause of cancer-associated mortality in women, and the incidence is on the rise worldwide. Asafoetida has shown a good anti-cancer activity against breast cancer in both in vivo and in vitro studies. Materials and Methods: For the evaluation of the cytotoxic effect of essential oil of asafoetida (EOA), MCF7 cells, a highly invasive variant of human breast cancer cell line, were exposed to different concentrations of EOA (2, 4, 6, 8, and 10 μl/ml) over different periods (24, 48, and 72 h), followed by cell viability analysis using 3-(4,5-Dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide (MTT) assay. For determining thein vivo toxicity of EOA, the oil was administered orally at doses of 0.1, 1, 10, and 100 μl/kg for 28 days in female Wistar rats. After completion of the experiment, hematological and serum biochemical parameters were evaluated and compared to the untreated group. Results: MTT assay results showed that EOA significantly decreased the viability of MCF7 cells in a time- and concentration-dependent manner, demonstrating a strong cytotoxic effect of EOA on breast cancer cells. In chronic toxicity study, the female Wistar rats showed no change in hematological and biochemical parameters at any of the administered dose. Conclusions: The cytotoxic effect of EOA on breast cancer cells, without general toxicity, makes it a promising compound as adjuvant therapy for breast cancer.
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