Rezaei-Seresht Hasan, Cheshomi Hamid, Falanji Farahnaz, Movahedi-Motlagh Fatemeh, Hashemian Maryam, Mireskandari Erfan
Traditional and Complementary Medicine Research Center, Sabzevar University of Medical Sciences, Sabzevar, Iran.
Cellular and Molecular Research Center, Faculty of Medicine, Sabzevar University of Medical Sciences, Sabzevar, Iran.
Avicenna J Phytomed. 2019 Nov-Dec;9(6):574-586. doi: 10.22038/AJP.2019.13475.
Phenolic compounds have been considered inhibitors of various cancers.
In this study, caffeic acid and gallic acid were appraised for their possible effects on apoptotic genes expression in a breast cancer cell line . We also evaluated ligand interaction and ligand binding with estrogen receptor alpha by molecular docking. To determine half maximal inhibitory concentration, MCF-7 cells were treated with different concentrations of caffeic acid and gallic acid by 3-(4, 5-dimethylthiazol-2-yl)-2, 5-diphenyltetrazolium bromide assay. Furthermore, morphological changes in cells and alterations in , and gene expression were studied by real-time RT-PCR. Also, protein network and different interactions between the desired genes were analyzed using GeneMANIA database.
Evaluation of cell survival by MTT assay revealed that the half-maximal inhibitory concentration values for caffeic acid and gallic acid against MCF-7 cells, were 159 and 18 µg/ml, respectively. These compounds were found to affect , and gene expression; this alteration in gene expression probably occurred along with the activation of intrinsic apoptotic signaling pathway.
Via apoptosis induction, caffeic acid and gallic acid have induce toxic effects and morphological changes in breast cancer cells, suggesting their possible future application as antitumor agents.
酚类化合物被认为是多种癌症的抑制剂。
在本研究中,评估了咖啡酸和没食子酸对乳腺癌细胞系中凋亡基因表达的可能影响。我们还通过分子对接评估了配体相互作用以及配体与雌激素受体α的结合。为了确定半数最大抑制浓度,采用3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四氮唑溴盐法用不同浓度的咖啡酸和没食子酸处理MCF-7细胞。此外,通过实时逆转录聚合酶链反应研究细胞的形态变化以及、和基因表达的改变。同时,使用GeneMANIA数据库分析蛋白质网络以及所需基因之间的不同相互作用。
通过MTT法评估细胞存活率显示,咖啡酸和没食子酸对MCF-7细胞的半数最大抑制浓度值分别为159和18μg/ml。发现这些化合物会影响、和基因表达;基因表达的这种改变可能与内源性凋亡信号通路的激活同时发生。
通过诱导凋亡,咖啡酸和没食子酸对乳腺癌细胞具有诱导毒性作用和形态变化,表明它们未来可能作为抗肿瘤药物应用。