首页> 外文期刊>International Journal of Environmental Research and Public Health >Preclinical Assessment of Vernonia amygdalina Leaf Extracts as DNA Damaging Anti-cancer Agent in the Management of Breast Cancer
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Preclinical Assessment of Vernonia amygdalina Leaf Extracts as DNA Damaging Anti-cancer Agent in the Management of Breast Cancer

机译:杏仁核病中的紫花苜蓿叶提取物作为DNA破坏性抗癌剂在乳腺癌治疗中的临床前评估

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Breast cancer is the leading cause of death among women between 40 and 55 years of age and is the second overall cause of death among women. Fortunately, the mortality rate from breast cancer has decreased in recent years due to an increased emphasis on early detection and more effective treatments. Despite early detection, conventional and chemotherapeutic methods of treatment, about 7% of women still died every year. Hence, the aim of the present study was to assess the therapeutic efficacy of vernonia amygdalina (VA) leaf extracts as anti-cancer agent against human breast cancer in vitro using the MTT [3-(4, 5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide] and alkaline single cell gel electrophoresis (Comet) assays, respectively. In this experiment, human breast adenocarcinoma (MCF-7) cells were treated with different doses of VA leaf extracts for 48 hours. Data obtained from the MTT assay showed that VA significantly ((P < 0.05) reduced the viability of MCF-7 cells in a dose-dependent manner upon 48 hours of exposure. Data generated from the comet assay also indicated a slight dose-dependent increase in DNA damage in MCF-7 cells associated with VA treatment. We observed a slight increase in comet tail-length, tail arm and tail moment, as well as in percentages of DNA cleavage at all doses tested, showing an evidence that VA-induced minimal genotoxic damage in MCF-7 cells. Taken together, our findings suggest that VA treatment moderately (P < 0.05) reduces cellular viability and induces minimal DNA damage in MCF-7 cells. These findings provide evidence that VA extracts represent a DNA-damaging anti-cancer agent against breast cancer and its mechanisms of action functions, at least in part, through minimal DNA damage and moderate toxicity in tumors cells.
机译:乳腺癌是40至55岁女性死亡的主要原因,也是女性死亡的第二大总体原因。幸运的是,由于越来越重视早期发现和更有效的治疗方法,近年来乳腺癌的死亡率有所下降。尽管有早期发现,常规治疗和化学治疗方法,每年仍有约7%的妇女死亡。因此,本研究的目的是使用MTT [3-(4,5-dimethylthiazol-2-yl)在体外评估紫花杏仁核(VA)叶提取物作为抗癌剂对人乳腺癌的治疗效果。 -2,5-二苯基四唑溴化物]和碱性单细胞凝胶电泳(Comet)分析。在该实验中,用不同剂量的VA叶提取物处理人乳腺癌细胞(MCF-7)48小时。从MTT试验获得的数据表明,暴露48小时后,VA以剂量依赖性方式显着降低(P <0.05)MCF-7细胞的活力,从彗星试验产生的数据也表明剂量依赖性略有增加VA处理对MCF-7细胞DNA损伤的影响,我们观察到彗星尾巴长度,尾臂和尾矩以及所有测试剂量下的DNA裂解百分比均略有增加,这表明VA诱导综上所述,我们的研究结果表明,适度(P <0.05)VA处理可降低MCF-7细胞的细胞活力并诱导最小的DNA损伤,这些发现提供了VA提取物代表DNA损伤的证据。抗乳腺癌的抗癌药及其作用机理至少部分通过对肿瘤细胞的DNA损伤最小和中等毒性来发挥作用。

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