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In vitro cytotoxic and apoptotic effect of Mimusops elengi Linn. methanolic bark extract

机译:Mimusops elengi Linn的体外细胞毒性和凋亡作用。甲醇树皮提取物

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The ayurvedic system of medicine recommends Mimusops elengi Linn. (Sapotaceae) for the treatment of tumors. The study is needed as cancer is the second most common cause for death in the world; most of the traditional drugs have shown resistance, low-cost approaches, and higher toxicity of the existing compound. The present study aims to determine the mode of cell death induced by the methanol extract of ME in human cancer cell lines. Among M.elengi (ME) crude extract and fractions screened for potential anticancer activity, MED and MEE fractions (dichloromethane and ethyl acetate) were found to have promising cytotoxic activities in all cell lines studied by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay and Suforhodamine B (SRB). MEE found to have more potent activity in cervical cancer (HeLa), colon cancer (HCT15), lung (A549), breast cancer (BT549), glioblastoma (U343 cells). Interestingly, ME was less cytotoxic in normal cell line (HBL-100) indicate the specific activity towards cancer cells. AO/EB staining and Hoechst-33342 staining indicate membrane blebbing, condensed and fragmented nuclei upon treatment with MEE and MED in HeLa, A549 and U343 cells. Fragmented DNA ladder and genomic DNA fragmentation were observed with DNA fragmentation assay based on gel electrophoresis and COMET assay by fluorescent microscopy. Similarly, cell cycle analysis by flow cytometer indicates distortion of normal cell cycle and increased subG0 phase. ME was found genotoxic by micronuclei formation. These results indicate that both MED and MEE fractions induces apoptosis but not necrosis cells in the cancer cells.
机译:阿育吠陀医学系统推荐Mimusops elengi Linn。 (Sapotaceae)用于治疗肿瘤。由于癌症是世界上第二大最常见的死亡原因,因此需要进行这项研究。大多数传统药物已显示出对现有化合物的耐药性,低成本方法和更高的毒性。本研究旨在确定由ME的甲醇提取物在人癌细胞系中诱导的细胞死亡模式。在M.elengi(ME)粗提取物和筛选出潜在抗癌活性的馏分中,发现MED和MEE馏分(二氯甲烷和乙酸乙酯)在3-(4,5-二甲基噻唑-2)研究的所有细胞系中均具有可观的细胞毒活性。 -yl)-2,5-二苯基溴化四氮唑(MTT)分析和亚磺胺大黄B(SRB)。 MEE在宫颈癌(HeLa),结肠癌(HCT15),肺癌(A549),乳腺癌(BT549),胶质母细胞瘤(U343细胞)中具有更强的活性。有趣的是,ME在正常细胞系(HBL-100)中的细胞毒性较小,表明其对癌细胞具有比活性。 AO / EB染色和Hoechst-33342染色表明在HeLa,A549和U343细胞中用MEE和MED处理后,膜起泡,细胞核浓缩和碎片化。通过基于凝胶电泳的DNA片段化分析和通过荧光显微镜的COMET分析,观察到片段化的DNA阶梯和基因组DNA片段化。同样,通过流式细胞仪进行的细胞周期分析表明正常细胞周期发生畸变,subG0期增加。通过微核形成发现ME具有遗传毒性。这些结果表明MED和MEE级分均诱导癌细胞中的凋亡,但不诱导坏死细胞。

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