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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 IIα in Human Hepatocarcinoma HepG-2 Cells
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β-Elemene Inhibits Cell Proliferation by Regulating the Expression and Activity of Topoisomerases I and IIα in Human Hepatocarcinoma HepG-2 Cells

机译:β-榄烯通过调节人肝癌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 of β-Elemene (β-ELE) on the proliferation, apoptosis, and topoisomerase I (TOPO I) and topoisomerase II? (TOPO llα) expression and activity of human hepatocarcinoma HepG-2 cells. Methods. After treatment with β-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 IIα was 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 of β-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 IIα in 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 TOPOI and TOPO IIα.
机译:客观的。探讨β-榄烯(β-ELE)对增殖,细胞凋亡和拓扑异构酶I(Topo I)和Topoisomerase II的影响吗? (TOPOLLα)人肝癌HEPG-2细胞的表达和活性。方法。在用β-ELE处理后,在倒置显微镜下观察到HepG-2细胞的形态改变。使用MTT测定评估细胞增殖,使用流式细胞术分析细胞循环,通过膜蛋白v / pi染色检测细胞凋亡。通过Western印迹技术分析Topo I和TopoIIα的表达,并使用Topo I介导的超核化的PBR322 DNA弛豫和TopoIIα介导的运动蛋白质DNA(KDNA)Decatenation测定测量它们的活性。还用于确定β-ELE对DNA断裂的直接效果的超级筛选的PBR322和KDNA。结果。 β-ELE以剂量和时间依赖的方式显着抑制Hepg-2细胞增殖。 β-ELE在S期,诱导细胞凋亡下诱导肿瘤细胞停滞,并以剂量​​依赖性方式下调Topo I和TopoIIα的蛋白质表达。 β-ELE还抑制了TOPO I-和TOPOIIα介导的DNA松弛,但没有直接诱导任何浓度的DNA断裂。结论。 β-ELE可以抑制HepG-2细胞的增殖,干扰TopoI和TopoIIα的表达和活性。

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