首页> 外文期刊>Journal of Cancer Treatment and Research >Ethyl Acetate Extract of Senna alata (L) Roxb Increases Cytotoxicity in the Human Breast, Prostate and Colorectal Cancer Cells
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Ethyl Acetate Extract of Senna alata (L) Roxb Increases Cytotoxicity in the Human Breast, Prostate and Colorectal Cancer Cells

机译:番泻叶(L)Roxb的乙酸乙酯提取物增加人乳腺癌,前列腺癌和结肠直肠癌细胞的细胞毒性。

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The objective of this study is to evaluate the effects of ethyl acetate extract of Senna alata (L) Roxb on some human carcinomas - MCF 7 (human breast), C4-2WT (prostate), HT 29 and HTC 116 (colorectal) cell lines. Screening assays carried out to determine cytotoxicity include: - MTT (3- (4, 5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide), clonogenic cell survival, Trypan Blue exclusion and methylene blue assays. Evaluation of the results showed that the extract strongly decreased the proliferation of the carcinoma cells in a dose-dependent manner. The minimum concentration of the extract required for 50% inhibition (GI_(50)) of the different cell lines calculated after MTT test were as follows: MCF-7 = 5.90 μg/ml, HCT 29 = 4.97 μg/ml, HCT 116 =11.86 μg/ml and C4-2WT = 9.48 μg/ml. Trypan Blue exclusion assay showed a decrease in the number of viable cells and an increase in the number of non-viable cells over 72 hrs post-treatment with the extract. Methylene blue assay showed that the number of viable cells, when their optical densities were measured over 72 hrs post-treatment, was reduced compared with the control. For clonogenic cell survival, there was an increase in cell proliferation and colony formation in the control cultures. However, cells treated with GI_(50) and 2X (twice) GI_(50) concentration of the extract showed a decrease in the number of colonies formed. The results indicate the cytotoxic potentials of the extract and therefore, suggests the use of ethyl acetate leaf extract of Senna alata (L) Roxb in preparing recipes for the management of cancer-related ailments.
机译:这项研究的目的是评估番泻叶Roxb乙酸乙酯提取物对某些人类癌症的影响-MCF 7(人类乳腺癌),C4-2WT(前列腺),HT 29和HTC 116(结肠直肠)细胞系。进行确定细胞毒性的筛选测定包括:-MTT(3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四唑溴化物),克隆形成细胞存活率,锥虫蓝排除法和亚甲基蓝测定法。结果评估表明,提取物以剂量依赖性方式强烈降低了癌细胞的增殖。在MTT试验后计算得出的不同细胞系的50%抑制(GI_(50))所需的最低提取物浓度如下:MCF-7 = 5.90μg/ ml,HCT 29 = 4.97μg/ ml,HCT 116 = 11.86μg/ ml,C4-2WT = 9.48μg/ ml。锥虫蓝排除试验显示,提取物处理后72小时内,活细胞数量减少,无活细胞数量增加。亚甲基蓝测定显示,与对照相比,当在处理后72小时内测量其光密度时,活细胞的数量减少了。对于克隆细胞存活,对照培养物中细胞增殖和集落形成增加。但是,用提取物的GI_(50)和2X(两倍)GI_(50)浓度处理的细胞显示形成的菌落数量减少。结果表明该提取物具有潜在的细胞毒性,因此,建议使用番泻叶(L)Roxb的乙酸乙酯叶提取物制备与癌症相关的疾病的治疗方法。

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