Jabbari Nasim, Ghoran Salar Hafez, Semsari Haniyeh, Hussen Bashdar Mahmud, Babaei Esmaeil
University of Tabriz, Faculty of Natural Science, Department of Animal Biology, Tabriz, Iran.
Golestan University, Faculty of Science, Department of Chemistry, Gorgan, Iran.
Turk J Pharm Sci. 2022 Jun 27;19(3):239-245. doi: 10.4274/tjps.galenos.2021.03502.
Gemini surfactant nanocurcumin (Gemini-Cur) is a novel formulation of Curcumin (Cur) with dramatic suppressive effects on cancer cells. Here, we investigated the cancer effects of Gemini-Cur in a human gastric adenocarcinoma cell-line (AGS) through the evaluation of the expression of long non-coding RNAs colon cancer-associated transcript-2 () and its downstream as known oncogenic modulators of tumorigenesis.
The AGS cells were treated with Gemini-Cur and pure Cur in a time- and dose-dependent manner. The toxicity of Gemini-Cur was studied using 3-(4,5-Dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide and scratch tests. Furthermore, real-time polymerase chain reaction and Western blotting techniques were employed to evaluate the expression of genes.
Gemini-Cur significantly affected the viability of AGS cells in a dose- and time-dependent manner with inhibitory concentration 50 values of 59.32, 40.88, and 19.63 µM during 24, 48, and 72 h, respectively. Our findings showed that Gemini-Cur effectively decreased the expression levels of and genes. Western blotting analysis also confirmed the down-regulation of in treated samples compared to controls.
Gemini-Cur attenuates the proliferation of AGS cells partly through modulation of the -related pathway.
Gemini表面活性剂纳米姜黄素(Gemini-Cur)是姜黄素(Cur)的一种新型制剂,对癌细胞具有显著的抑制作用。在此,我们通过评估长链非编码RNA结肠癌相关转录本2( )及其下游作为已知肿瘤发生致癌调节因子的表达,研究了Gemini-Cur对人胃腺癌细胞系(AGS)的癌症影响。
AGS细胞以时间和剂量依赖性方式用Gemini-Cur和纯Cur处理。使用3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四氮唑溴盐和划痕试验研究Gemini-Cur的毒性。此外,采用实时聚合酶链反应和蛋白质印迹技术评估基因的表达。
Gemini-Cur以剂量和时间依赖性方式显著影响AGS细胞的活力,在24、48和72小时期间的半数抑制浓度值分别为59.32、40.88和19.63 μM。我们的研究结果表明,Gemini-Cur有效降低了 和 基因的表达水平。蛋白质印迹分析也证实,与对照相比,处理样品中 表达下调。
Gemini-Cur部分通过调节 相关途径减弱AGS细胞的增殖。