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Rhizoma Paridis Saponins Induces Cell Cycle Arrest and Apoptosis in Non-Small Cell Lung Carcinoma A549 Cells

机译:根茎皂苷诱导非小细胞肺癌A549细胞的细胞周期阻滞和凋亡

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BACKGROUND As a traditional Chinese medicine herb, Chonglou ([i]Paris polyphylla var. chensiins[/i]) has been used as anticancer medicine in China in recent decades, as it can induce cell cycle arrest and apoptosis in numerous cancer cells. The saponins extract from the rhizoma of Chonglou [[i]Rhizoma Paridis[/i] saponins (RPS)] is known as the main active component for anticancer treatment. However, the molecular mechanism of the anticancer effect of RPS is unknown. MATERIAL AND METHODS The present study evaluated the effect of RPS in non-small-cell lung cancer (NSCLC) A549 cells using the 3-(4,5-dimethylthiazol-2-yl) -2,5-diphenyl tetrazolium bromide (MTT) assay and flow cytometry. Subsequently, the expression of several genes associated with cell cycle and apoptosis were detected by reverse transcription-quantitative polymerase chain reaction (qRT-PCR) and Western blotting. RESULTS RPS was revealed to inhibit cell growth, causing a number of cells to accumulate in the G 1 phase of the cell cycle, leading to apoptosis. In addition, the effect was dose-dependent. Moreover, the results of qRT-PCR and Western blotting showed that p53 and cyclin-dependent kinase 2 (CDK2) were significantly downregulated, and that BCL2, BAX, and p21 were upregulated, by RPS treatment. CONCLUSIONS We speculated that the RPS could act on a pathway, including p53, p21, BCL2, BAX, and CDK2, and results in G1 cell cycle arrest and apoptosis in NSCLC cells.
机译:背景技术作为一种传统中草药,近几十年来,崇楼([i] Paris polyphylla var.chensiins [/ i])已在中国用作抗癌药,因为它可以诱导许多癌细胞的细胞周期停滞和凋亡。从崇楼根中提取的皂苷[[i] Rhizoma Paridis [/ i]皂苷(RPS)]被称为抗癌治疗的主要活性成分。但是,RPS抗癌作用的分子机制尚不清楚。材料与方法本研究使用3-(4,5-二甲基噻唑-2-基)-2,5-二苯基溴化四氮唑(MTT)评估了RPS在非小细胞肺癌(NSCLC)A549细胞中的作用。分析和流式细胞仪。随后,通过逆转录-定量聚合酶链反应(qRT-PCR)和蛋白质印迹检测了与细胞周期和凋亡相关的几个基因的表达。结果显示RPS抑制细胞生长,导致许多细胞在细胞周期的G 1期蓄积,从而导致细胞凋亡。此外,效果是剂量依赖性的。而且,qRT-PCR和蛋白质印迹的结果表明,通过RPS处理,p53和细胞周期蛋白依赖性激酶2(CDK2)显着下调,而BCL2,BAX和p21上调。结论我们推测RPS可以作用于p53,p21,BCL2,BAX和CDK2等途径,并导致NSCLC细胞的G1细胞周期停滞和凋亡。

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