阿魏提取物对PC12和MCF7癌细胞的抗增殖作用

M. Abroudi, Amir Ganji Fard, G. Dadashizadeh, Omid Gholami, D. Mahdian
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引用次数: 8

摘要

背景:阿魏(Ferula assa-foetida)是伞形科的一种草本植物,具有广泛的生物活性,对多种癌症具有防腐、抗菌、抗炎、抗肿瘤等活性。在这些特征中,抗肿瘤活性近年来变得越来越重要,但仍需要更多的研究来解决其潜在的机制。目的:研究阿魏对PC12和MCF7细胞的抑制增殖作用,并探讨其作用机制。材料和方法:细胞在含10%胎牛血清、100单位/ml青霉素、100µg/ml链霉素的DMEM培养基中培养。用不同浓度的阿魏乙醇提取物孵育细胞。MTT染色检测细胞毒性,PI染色检测细胞凋亡。结果:MTT实验结果显示,与对照组相比,10、7、5、2.5 μM浓度的阿魏乙醇提取物对PC12和MCF7细胞的活性和诱导凋亡均有显著影响。结论:本研究确定不同浓度阿魏通过诱导凋亡抑制PC12和MCF7细胞的生长,降低细胞活力,并呈时间和剂量依赖性。然而,阿魏提取物诱导细胞凋亡的机制还有待进一步研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Antiproliferative Effects of Ferula assa-foetida’s Extract on PC12 and MCF7 Cancer Cells
Background: Ferula assa-foetida is a herbaceous plant of the Umbelliferae family having a broad spectrum of biological activities such as antiseptic, antibacterial, anti-inflammation, and, anti-tumor activity against a wide range of cancers. Among these features, antitumor activity has become more important in recent years and it still demands more investigations to address the underlying mechanisms. Purpose: This current study was conducted to evaluate the anti-proliferative effect of Ferula assa-foetida on PC12 and MCF7 cells as well as examining its mechanisms. Materials and Methods: Cells were cultured in DMEM medium with 10% fetal bovine serum, 100 units/ml penicillin, and 100 µg/ml streptomycin. Cells incubated with different concentrations of the ethanolic extract of Ferula assa-foetida. Notably, cytotoxicity and apoptosis assay were measured by MTT and PI staining, respectively. Results: The MTT results showed that the ethanolic extract of Ferula assa-foetida in concentrations of 10, 7, 5, and 2.5 μM on both PC12 and MCF7 cells had a significant effect in cell viability and apoptosis induction in comparison to control group. Conclusion: In this study, it was determined that Ferula assa-fetida through the induction of apoptosis prevented the growth of PC12 and MCF7 cells and made a reduction in cell viability with different concentrations in a time- and dose-dependent manner. However, more studies are needed to reveal the mechanisms of Ferula assa-foetida’s extract in apoptosis induction.
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