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首页> 外文期刊>Molecular medicine reports >Antiproliferative effects of anastrozole on MCF-7 human breast cancer cells in vitro are significantly enhanced by combined treatment with testosterone undecanoate
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Antiproliferative effects of anastrozole on MCF-7 human breast cancer cells in vitro are significantly enhanced by combined treatment with testosterone undecanoate

机译:十一酸睾丸激素联合治疗可显着增强阿那曲唑对体外MCF-7人乳腺癌细胞的抗增殖作用

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摘要

The present study aimed to assess the effects of aromatase inhibitor anastrozole and testosterone undecanoate, separately and in combination, on proliferation and apoptosis in MCF-7 human breast cancer cells cultured in vitro. The effects of various concentrations of these drugs on the proliferation of MCF-7 cells were evaluated by CCK8 assay, the levels of cell apoptosis were evaluated by flow cytometry with Annexin-V/propidium iodide staining and androgen receptor (AR) protein expression was determined by western blot analysis. The results of the CCK8 assay indicated that greater antiproliferative activity was detected in the MCF-7 cells in the combined treatment groups, compared with those treated with anastrozole or testosterone undecanoate alone. Flow cytometric analysis of apoptosis revealed that treatment with a combination of the two drugs generated a higher percentage of apoptotic cells, particularly when the two drugs were applied for 48 h, compared with single drug treatment. Western blot analysis revealed a significant decrease in AR protein expression in the combined treatment groups compared with MCF7 cells treated with single drugs. The results of the present study provided evidence supporting the potential of a combination of anastrozole and testosterone undecanoate as a novel therapeutic strategy for the treatment of breast cancer. Furthermore, it was demonstrated that the antiproliferative effects of anastrozole were significantly enhanced by combined treatment with testosterone undecanoate via the AR signaling pathway.
机译:本研究旨在评估芳香酶抑制剂阿那曲唑和十一酸睾丸酮分别或组合对体外培养的MCF-7人乳腺癌细胞增殖和凋亡的影响。通过CCK8试验评估了不同浓度的这些药物对MCF-7细胞增殖的影响,通过Annexin-V /碘化丙啶染色的流式细胞术评估了细胞凋亡水平,并确定了雄激素受体(AR)蛋白的表达。通过蛋白质印迹分析。 CCK8分析的结果表明,与单独使用阿那曲唑或十一烷酸睾丸酮治疗的组相比,在联合治疗组的MCF-7细胞中检测到了更高的抗增殖活性。细胞凋亡的流式细胞仪分析表明,与单药治疗相比,两种药物联合治疗可产生更高百分比的凋亡细胞,特别是当两种药物应用48 h时。 Western blot分析显示,与单药治疗的MCF7细胞相比,联合治疗组的AR蛋白表达显着降低。本研究的结果提供了证据支持阿那曲唑和十一酸睾丸激素的组合作为治疗乳腺癌的新型治疗策略的潜力。此外,已经证明,通过AR信号传导途径与十一酸睾丸激素联合治疗显着增强了阿那曲唑的抗增殖作用。

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