首页> 美国卫生研究院文献>BioMed Research International >A Study on Cytotoxic and Apoptotic Potential of a Triterpenoid Saponin (3-O-α-L-Arabinosyl Oleanolic Acid) Isolated from Schumacheria castaneifolia Vahl in Human Non-Small-Cell Lung Cancer (NCI-H292) Cells
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A Study on Cytotoxic and Apoptotic Potential of a Triterpenoid Saponin (3-O-α-L-Arabinosyl Oleanolic Acid) Isolated from Schumacheria castaneifolia Vahl in Human Non-Small-Cell Lung Cancer (NCI-H292) Cells

机译:分离自美人鱼鳞茎的三萜皂苷(3-O-α-L-阿拉伯糖基齐墩果酸)在人非小细胞肺癌(NCI-H292)细胞中的细胞毒性和凋亡潜力的研究

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摘要

Lung cancer is the major cause of cancer death among men. A number of natural compounds have proven to be useful in the treatmet of lung cancer. This study was aimed to determine cytotoxic and apoptotoic effects of a natural compound 3-O-α-L-arabinosyl oleanolic acid (3-O-L-AO) isolated from Schumacheria castaneifolia in non-small-cell lung cancer (NCI-H292) cells. Cytotoxic effects of 3-O-L-AO were determined by Sulforhodamine B (SRB) assay and apoptotic effects were tested by evaluating (a) apoptotsis related morphological changes, (b) caspase 3/7 activity, and (c) expression of Bax, p53, and survivin genes. Oxidative stress markers (reactive oxygen species (ROS), glutathione-S-transferase (GST), and glutathione (GSH)) were also analysed in 3-O-L-AO treated NCI-H292 cells. 3-O-L-AO exerted potent cytotoxic effects in NCI-H292 cells while being less cytotoxic to normal lung (MRC-5) cells. Exposure to 3-O-L-AO caused upregulation of Bax and p53 and downregulation of survivin in NCI-H292 cells. Activation of caspase 3/7 and morphological features related to apoptosis further confirmed 3-O-L-AO induced apoptosis. Furthermore, elevated ROS and GST levels and decreased GSH levels suggested 3-O-L-AO can induce apoptosis, possibly causing oxidative stress in NCI-H292 cells. Overall results suggest that 3-O-L-AO can be considered as an effective anticancer agent for the treatment of lung cancer.
机译:肺癌是男性癌症死亡的主要原因。已证明许多天然化合物可用于肺癌治疗。这项研究旨在确定从Schumacheria castaneifolia分离的天然化合物3-O-α-L-阿拉伯糖基齐墩果酸(3-OL-AO)在非小细胞肺癌(NCI-H292)细胞中的细胞毒性和凋亡作用。用磺胺多巴胺B(SRB)测定法测定3-OL-AO的细胞毒性作用,并通过评估(a)凋亡相关的形态变化,(b)caspase 3/7活性和(c)Bax,p53的表达来测试凋亡的作用和survivin基因。还分析了在3-O-L-AO处理的NCI-H292细胞中的氧化应激标记(活性氧(ROS),谷胱甘肽S-转移酶(GST)和谷胱甘肽(GSH))。 3-O-L-AO在NCI-H292细胞中具有强大的细胞毒性作用,而对正常肺(MRC-5)细胞的细胞毒性较小。暴露于3-O-L-AO会导致NCI-H292细胞中Bax和p53的上调以及survivin的下调。 caspase 3/7的激活和与凋亡相关的形态学特征进一步证实了3-O-L-AO诱导的凋亡。此外,升高的ROS和GST水平和降低的GSH水平表明3-O-L-AO可以诱导细胞凋亡,可能在NCI-H292细胞中引起氧化应激。总体结果表明,3-O-L-AO可被视为治疗肺癌的有效抗癌药。

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