Orangi Mona, Pasdaran Ardalan, Shanehbandi Dariush, Kazemi Tohid, Yousefi Bahman, Hosseini Behnaz-Alsadat, Baradaran Behzad
Immunology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran; Tabriz University of Medical Sciences, International Branch of Aras, Tabriz, Iran.
Medical Plant Processing Research Center, Shiraz University of Medical Sciences, Shiraz, Iran; Department of Pharmacognosy, Faculty of Pharmacy, Guilan University of Medical Sciences, Rasht, Iran.
Evid Based Complement Alternat Med. 2016;2016:8540640. doi: 10.1155/2016/8540640. Epub 2016 Feb 29.
Herbs have played a positive role in medicine for thousands of years. In the current study, we investigated the cytotoxicity effects of Scrophularia oxysepala methanolic subfractions and the underlying mechanism responsible for cell death in human breast carcinoma (MCF-7 cells) and mouse fibrosarcoma (WEHI-164 cells). From 60% and 80% methanolic fractions, four subfractions (Fa, Fb, Fc, and Fd), yielded from size exclusion by Sephadex-LH20 column chromatography, were chosen. MTT assay revealed that all subfractions significantly reduced cell viability after 24 h and 36 h in a dose-dependent manner; it is worth noting that Fa and Fb subfractions had the highest cytotoxicity, with IC50 values of 52.9 and 61.2 μg/mL in MCF-7 at 24 h, respectively. ELISA, TUNEL, and DNA fragmentation assay revealed that antiproliferative effects of all subfractions were associated with apoptosis on cancer cells, without any significant effect on L929 normal cells. qRT-PCR data showed that, after 24 h treatment with IC50 concentrations of the subfractions, caspase-3 expression was increased in cancer cells while the expression of Bcl-2 was decreased. S. oxysepala methanolic subfractions induce apoptosis in MCF-7 and WEHI-164 cells and could be considered as a source of natural anticancer agents.
数千年来,草药在医学中发挥了积极作用。在当前的研究中,我们调查了玄参甲醇亚组分的细胞毒性作用以及人乳腺癌(MCF-7细胞)和小鼠纤维肉瘤(WEHI-164细胞)中细胞死亡的潜在机制。从60%和80%的甲醇组分中,选择通过Sephadex-LH20柱色谱法进行尺寸排阻得到的四个亚组分(Fa、Fb、Fc和Fd)。MTT分析显示,所有亚组分在24小时和36小时后均以剂量依赖性方式显著降低细胞活力;值得注意的是,Fa和Fb亚组分具有最高的细胞毒性,在24小时时,MCF-7细胞中的IC50值分别为52.9和61.2μg/mL。ELISA、TUNEL和DNA片段化分析显示,所有亚组分的抗增殖作用均与癌细胞凋亡相关,而对L929正常细胞无任何显著影响。qRT-PCR数据显示,用亚组分的IC50浓度处理24小时后,癌细胞中caspase-3的表达增加,而Bcl-2的表达降低。玄参甲醇亚组分可诱导MCF-7和WEHI-164细胞凋亡,可被视为天然抗癌剂的来源。