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The Purified Extract from the Medicinal Plant Bacopa monnieri, Bacopaside II, Inhibits Growth of Colon Cancer Cells In Vitro by Inducing Cell Cycle Arrest and Apoptosis

机译:来自药用植物Bacopa Monnieri,Bacopaside II的纯化提取物,通过诱导细胞周期停滞和细胞凋亡来抑制体外结肠癌细胞的生长

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摘要

Aquaporin-1 (AQP1), a transmembrane pore-forming molecule, facilitates the rapid movement of water and small solutes across cell membranes. We have previously shown that bacopaside II, an extract from the medicinal herb Bacopa monnieri, blocks the AQP1 water channel and impairs migration of cells that express AQP1. The aim of this study was to further elucidate the anti-tumour potential of bacopaside II in colon cancer cells. Expression of AQP1 in HT-29, SW480, SW620 and HCT116 was determined by quantitative PCR and western immunoblot. Cells were treated with bacopaside II, and morphology, growth, autophagy, cell cycle and apoptosis assessed by time-lapse microscopy, crystal violet, acridine orange, propidium iodide (PI) and annexin V/PI staining respectively. AQP1 expression was significantly higher in HT-29 than SW480, SW620 and HCT116. Bacopaside II significantly reduced growth at ≥20 µM for HT-29 and ≥15 µM for SW480, SW620 and HCT116. Inhibition of HT-29 at 20 µM was primarily mediated by G0/G1 cell cycle arrest, and at 30 µM by G2/M arrest and apoptosis. Inhibition of SW480, SW620 and HCT116 at ≥15 µM was mediated by G2/M arrest and apoptosis. These results are the first to show that bacopaside II inhibits colon cancer cell growth by inducing cell cycle arrest and apoptosis.
机译:Aquaporin-1(AQP1),跨膜孔形成分子,促进水和小溶质穿过细胞膜的快速运动。我们之前已经表明,Bacopaside II,来自药物草本Bacopa Monnieri的提取物,阻断AQP1水通道并损害表达AQP1的细胞的迁移。本研究的目的是进一步阐明结肠癌细胞中巴卡西肽II的抗肿瘤潜力。通过定量PCR和Western免疫印迹测定HT-29,SW480,SW620和HCT116中AQP1的表达。用稳定显微镜,晶体紫,吖啶橙,碘化丙酰基(PI)和膜蛋白v / Pi染色分别用止匹匹配II II处理细胞,以及通过延时显微镜,晶体,吖啶,橙子,碘化丙啶(PI)和膜蛋白v / Pi染色来评估的形态学,生长,自噬,细胞周期和细胞凋亡。 HT-29的AQP1表达明显高于SW480,SW620和HCT116。对于SW480,SW620和HCT116,HT-29和≥15μm的≥20μm显着降低了≥20μm的生长。 HT-29在20μm的抑制主要由G0 / G1细胞循环骤停介导,并且通过G2 / M停止和细胞凋亡为30μm。抑制SW480,SW620和HCT116,≥15μm的抑制和凋亡介导。这些结果是首先表明通过诱导细胞循环骤停和细胞凋亡来抑制结肠癌II抑制结肠癌细胞生长。

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