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Influence of Tanshinone IIA on the Apoptosis of Human Esophageal Ec-109 Cells

机译:丹参酮IIA对人食管Ec-109细胞凋亡的影响

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摘要

The induced-apoptosis effect and mechanism of human esophageal cancer Ec-109 cells via tanshinone IIA was investigated. The Ec-109 cells were cultured in vitro with different concentrations of tanshinone IIA (2 mu g/mL, 4 mu g/mL, or 8 mu g/mL) for 12, 24, 36, and 48 hours. MTT assay was used to evaluate the proliferative inhibition rate of tanshinone HA on esophageal Ec-109 cells. After 24 hours of culturing in vitro, a control group was assigned. The apoptosis rate was detected by the AO/EB and annexin V-FITC/propidium iodide assay, and the protein levels of Caspase-4 and CHOP were determined by the Western blot technique. NUT data showed that tanshinone HA could significantly inhibit the proliferation of Ec-109 cells with a dose- and time-dependent mode. Compared with the control group, tanshinone IIA could apparently induce apoptosis of Ec-109 cells, and the level of Caspase-4 and CHOP (p<0.01) obviously increased. Tanshinone HA can significantly induce the apoptosis of Ec-109 cells, which may take effect by the stress pathway of the endoplasmic reticulum.
机译:研究了丹参酮IIA对人食管癌Ec-109细胞的诱导凋亡作用及其机制。将Ec-109细胞与不同浓度的丹参酮IIA(2微克/毫升,4微克/毫升或8微克/毫升)体外培养12、24、36和48小时。 MTT法用于评价丹参酮HA对食管Ec-109细胞的增殖抑制率。体外培养24小时后,分配对照组。通过AO / EB和膜联蛋白V-FITC /碘化丙啶检测细胞凋亡率,并通过蛋白质印迹技术测定Caspase-4和CHOP的蛋白水平。 NUT数据显示,丹参酮HA可以剂量和时间依赖性方式显着抑制Ec-109细胞的增殖。与对照组相比,丹参酮IIA可明显诱导Ec-109细胞凋亡,Caspase-4和CHOP水平明显升高(p <0.01)。丹参酮HA可以显着诱导Ec-109细胞凋亡,可能通过内质网的应激途径起作用。

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