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Effect of cortisol on cell proliferation and the expression of lipoprotein lipase and vascular endothelial growth factor in a human osteosarcoma cell line.

机译:皮质醇对人骨肉瘤细胞系细胞增殖以及脂蛋白脂肪酶和血管内皮生长因子表达的影响。

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PURPOSE: The aim of this study is to investigate whether cortisol inhibited cell proliferation and the expressions of lipoprotein lipase (LPL), a key enzyme involved in the energy metabolism in tumor cells, and vascular endothelial growth factor (VEGF), a potent angiogenic factor in the tumor, in cultures of OST cells, a human osteosarcoma cell line. METHODS: OST cells were treated for 48 h with or without cortisol. To examine the effect of cortisol on cell proliferation, the expression of proliferating cell nuclear antigen (PCNA) was examined by Western blotting, and the amount of (3)H-thymidine incorporated into DNA during the last 30 min of the 48-h treatment period was measured. To examine the effect of cortisol on the expression of LPL, the activity and mass of LPL were measured in the extract of acetone/ether powder of cells, and the amount of (35)S-methionine incorporated into LPL during the last 2 h of the 48-h treatment period was measured by immunoprecipitation. The expression of VEGF was examined by immunohistochemistry and Western blotting. RESULTS: The amount of (3)H-thymidine incorporated into DNA and the level of PCNA were lower in the cortisol-treated cultures than in the untreated cultures, thus indicating that cortisol inhibited the proliferation of OST cells. The synthetic rate and activity of LPL were lower in the cortisol-treated cultures than in the untreated cultures but no difference in the specific activity of LPL between the two cultures was observed, thus indicating that cortisol inhibited LPL synthesis, thereby resulting in a decreased LPL activity. The expression of VEGF was lower in the cortisol-treated cultures than in the untreated cultures. CONCLUSION: Cortisol not only has the ability to inhibit cell proliferation but also the ability to inhibit the expressions of LPL and VEGF in cultures of OST cells.
机译:目的:本研究的目的是研究皮质醇是否抑制细胞增殖以及脂蛋白脂酶(LPL)(一种参与肿瘤细胞能量代谢的关键酶)和血管内皮生长因子(VEGF)(一种有效的血管生成因子)的表达在肿瘤中,在人骨肉瘤细胞系OST细胞中。方法:在有或没有皮质醇的情况下,将OST细胞处理48小时。为了检查皮质醇对细胞增殖的影响,通过蛋白质印迹法检测增殖的细胞核抗原(PCNA)的表达,以及在48小时处理的最后30分钟内掺入DNA中的(3)H-胸苷的量期间进行了测量。为了检查皮质醇对LPL表达的影响,在细胞的丙酮/醚粉提取物中测量了LPL的活性和质量,并在最后的2小时内测定了向LPL中掺入的(35)S-甲硫氨酸的量。通过免疫沉淀测定48小时的治疗时间。通过免疫组织化学和Western印迹检查VEGF的表达。结果:在皮质醇处理的培养物中,掺入DNA的(3)H-胸腺嘧啶核苷的量和PCNA的水平低于未处理的培养物中,因此表明皮质醇抑制了OST细胞的增殖。皮质醇处理的培养物中LPL的合成速率和活性均低于未处理的培养物,但在两种培养物中LPL的比活性没有观察到差异,因此表明皮质醇抑制了LPL的合成,从而导致LPL的降低活动。在皮质醇处理的培养物中,VEGF的表达低于未处理的培养物中。结论:皮质醇不仅具有抑制细胞增殖的能力,而且具有抑制OST细胞培养物中LPL和VEGF表达的能力。

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