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首页> 外文期刊>BioMed research international >β-Elemene Inhibits Cell Proliferation by Regulating the Expression and Activity of Topoisomerases I and IIαin Human Hepatocarcinoma HepG-2 Cells
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β-Elemene Inhibits Cell Proliferation by Regulating the Expression and Activity of Topoisomerases I and IIαin Human Hepatocarcinoma HepG-2 Cells

机译:β-榄香烯通过调节人肝癌HepG-2细胞中拓扑异构酶I和IIα的表达和活性来抑制细胞增殖

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Objective. To investigate the effects ofβ-Elemene (β-ELE) on the proliferation, apoptosis, and topoisomerase I (TOPO I) and topoisomerase IIα(TOPO IIα) expression and activity of human hepatocarcinoma HepG-2 cells.Methods. After treatment withβ-ELE, morphological alterations of HepG-2 cells were observed under an inverted microscope. Cell proliferation was assessed using an MTT assay, cell cycles were analyzed using flow cytometry, and apoptosis was detected by Annexin V/PI staining. The expression of TOPO I and TOPO IIαwas analyzed by Western blot techniques, and their activity was measured using the TOPO I-mediated, supercoiled pBR322 DNA relaxation and TOPO IIα-mediated Kinetoplast DNA (kDNA) decatenation assays, respectively. Supercoiled pBR322 and kDNA were also used to determine the direct effect ofβ-ELE on DNA breaks.Results.β-ELE significantly inhibited HepG-2 cell proliferation in a dose- and time-dependent manner.β-ELE also induced tumor cell arrest at S phase, induced cell apoptosis, and downregulated the protein expression of TOPO I and TOPO IIαin a dose-dependent manner.β-ELE also inhibited TOPO I- and TOPO IIα-mediated DNA relaxation but did not directly induce DNA breakage at any concentration.Conclusion.β-ELE could inhibit the proliferation of HepG-2 cells and interfere with the expression and activity of TOPO I and TOPO IIα.
机译:目的。探讨β-榄香烯(β-ELE)对人肝癌HepG-2细胞增殖,凋亡和拓扑异构酶I(TOPO I)和拓扑异构酶IIα(TOPOIIα)表达及活性的影响。用β-ELE处理后,在倒置显微镜下观察到HepG-2细胞的形态变化。使用MTT测定法评估细胞增殖,使用流式细胞术分析细胞周期,并通过膜联蛋白V / PI染色检测凋亡。通过蛋白质印迹技术分析TOPO I和TOPOIIα的表达,并分别使用TOPO I介导的超螺旋pBR322 DNA弛豫和TOPOIIα介导的Kinetoplast DNA(kDNA)脱脂测定法测量其活性。还使用超螺旋pBR322和kDNA来确定β-ELE对DNA断裂的直接作用。结果:β-ELE以剂量和时间依赖性方式显着抑制HepG-2细胞的增殖。 S期诱导细胞凋亡,并以剂量​​依赖的方式下调TOPO I和TOPOIIα的蛋白表达.β-ELE也抑制TOPO I-和TOPOIIα介导的DNA松弛,但在任何浓度下均不直接诱导DNA断裂。结论:β-ELE可以抑制HepG-2细胞的增殖,并干扰TOPO I和TOPOIIα的表达和活性。

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