Mirmalek Seyed Abbas, Faraji Sholeh, Ranjbaran Sanaz, Aryan Hoda, Arani Hamid Zaferani, Jangholi Ehsan, Marzouni Hadi Zare, Salimi-Tabatabaee Seyed Alireza
Department of Surgery, Tehran Medical Sciences, Islamic Azad University, Tehran, Iran.
Young Researchers and Elite Club, Tehran Medical Sciences, Islamic Azad University, Tehran, Iran.
Arch Med Sci. 2020 Mar 19;19(4):1092-1098. doi: 10.5114/aoms.2020.93789. eCollection 2023.
Breast cancer is the major leading cause of death from cancer among women. Given the drug resistance seen during the treatment of this disease, it is very important to identify new therapies and new anticancer drugs. Some studies indicate the cytotoxic effects of cyanidin 3-glycoside (C3G). Therefore, this study aims to evaluate the anticancer effect of C3G in the treatment of the MCF-7 cell line.
In this study, the MCF-7 cell line was treated with different concentrations of C3G for 24 and 48 h. Assessment of cell death was performed by MTT assay. The cell apoptosis rate was measured using an Annexin V/propidium iodide assay through flow cytometry. The expression levels of , , , , , and genes were evaluated using polymerase chain reaction, and Western blotting was performed for CYP1 to confirm the results.
Our findings showed that C3G has dose-dependent cytotoxic effects on the MCF-7 cell line. According to flow cytometry results, the apoptosis of the cells 24 h after exposure to C3G was more than 51.5%. Moreover, after 24 h of exposure to the half-maximal inhibitory concentration of C3G, the expression of , , , , and genes increased, and the expression of gene decreased. The Western blotting showed that CYP1 protein increased 2-fold compared to the control sample.
The results of this study demonstrated that C3G has apoptotic and cytotoxic effects on breast cancer cells. Therefore, it is likely that this substance could be a suitable option for cancer therapy.
乳腺癌是女性癌症死亡的主要原因。鉴于在这种疾病治疗过程中出现的耐药性,识别新的治疗方法和新型抗癌药物非常重要。一些研究表明矢车菊素3-糖苷(C3G)具有细胞毒性作用。因此,本研究旨在评估C3G在治疗MCF-7细胞系中的抗癌作用。
在本研究中,用不同浓度的C3G处理MCF-7细胞系24小时和48小时。通过MTT法评估细胞死亡情况。使用膜联蛋白V/碘化丙啶法通过流式细胞术测量细胞凋亡率。使用聚合酶链反应评估、、、、、和基因的表达水平,并进行CYP1的蛋白质印迹以确认结果。
我们的研究结果表明,C3G对MCF-7细胞系具有剂量依赖性细胞毒性作用。根据流式细胞术结果,暴露于C3G 24小时后细胞凋亡率超过51.5%。此外,在暴露于C3G半数最大抑制浓度24小时后,、、、和基因的表达增加,而基因的表达下降。蛋白质印迹显示,与对照样品相比,CYP1蛋白增加了2倍。
本研究结果表明,C3G对乳腺癌细胞具有凋亡和细胞毒性作用。因此,这种物质很可能是癌症治疗的合适选择。