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Effects of all-trans-retinoic on human gastric cancer cells BGC-823.

机译:全反式维甲酸对人胃癌细胞BGC-823的影响。

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摘要

OBJECTIVE: To determine the inhibitory effects of all-trans-retinoic acid (ATRA) on cell growth, cell cycle and vascular endothelial growth factor (VEGF) expression in the human gastric cancer cell line BGC-823 in vitro. METHODS: Human gastric cancer BGC-823 cells were treated with various concentrations of ATRA and the cell growth was then determined using the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide viability assay. The cell cycle distribution was analyzed using a flow cytometer. The VEGF mRNA and protein expression were analyzed by semi-quantitative RT-PCR and Western blotting, respectively. RESULTS: ATRA at concentrations of 0.1-10 micromol/L inhibited the growth of BGC-823 cells grown in culture; a time- and dose-dependent inhibitory influence was found. ATRA arrested BGC-823 cells at the G0/G1 phase in a dose-dependent way. Both VEGF mRNA and protein were decreased by ATRA in a dose-dependent way. CONCLUSION: The anti-tumor effects of ATRA on human gastric cancer cells are associated with G0/G1 phase arrest and decreased VEGF expression.
机译:目的:探讨全反式维甲酸(ATRA)对人胃癌细胞BGC-823细胞生长,细胞周期和血管内皮生长因子(VEGF)表达的抑制作用。方法:用不同浓度的ATRA处理人胃癌BGC-823细胞,然后使用3-(4,5-二甲基噻唑-2-基)-2,5-二苯基溴化四唑活力测定法测定细胞生长。使用流式细胞仪分析细胞周期分布。分别通过半定量RT-PCR和Western印迹分析VEGF mRNA和蛋白表达。结果:ATRA浓度为0.1-10μmol/ L可抑制培养的BGC-823细胞的生长。发现了时间和剂量依赖性抑制作用。 ATRA以剂量依赖性方式将BGC-823细胞阻滞在G0 / G1期。 VEGF mRNA和蛋白均被ATRA降低,呈剂量依赖性。结论:ATRA对人胃癌细胞的抗肿瘤作用与G0 / G1期阻滞和VEGF表达降低有关。

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