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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:通过组合治疗,睾酮未成熟的组合治疗显着提高了Anstrozole对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:本研究旨在评估芳族酶抑制剂Anastrozole和睾酮未赤烷酸酯,单独和组合的影响,对体外培养的MCF-7人乳腺癌细胞的增殖和凋亡。通过CCK8测定评估各种浓度这些药物对MCF-7细胞增殖的影响,通过用膜蛋白-V /碘化丙啶染色和雄激素受体(AR)蛋白表达来评价细胞凋亡的水平通过Western印迹分析。 CCK8测定的结果表明,与单独用Anstrozole或睾酮未异癸酸异癸酸处理的那些相比,在组合治疗组中的MCF-7细胞中检测到更大的抗增殖活性。细胞凋亡的流式细胞术分析显示,两种药物组合的治疗产生了更高百分比的凋亡细胞,特别是当两种药物施用48小时时,与单一药物处理相比。与用单一药物处理的MCF7细胞相比,蛋白质印迹分析显示组合治疗组中Ar蛋白表达的显着降低。本研究的结果提供了证据,这些证据支持潜在的Anstrozole和睾酮未异甘蔗作为一种用于治疗乳腺癌的新疗效策略。此外,证明通过通过AR信号通路与睾酮未异癸酸化合物的组合治疗显着提高了Anstrozole的抗增殖效果。

著录项

  • 来源
    《Molecular medicine reports》 |2015年第1期|共7页
  • 作者单位

    Peking Univ Dept Breast Surg Shenzhen Hosp Shenzhen 518036 Guangdong Peoples R China;

    Peking Univ Dept Breast Surg Shenzhen Hosp Shenzhen 518036 Guangdong Peoples R China;

    Peking Univ Dept Breast Surg Shenzhen Hosp Shenzhen 518036 Guangdong Peoples R China;

    Peking Univ Dept Breast Surg Shenzhen Hosp Shenzhen 518036 Guangdong Peoples R China;

    Peking Univ Dept Breast Surg Shenzhen Hosp Shenzhen 518036 Guangdong Peoples R China;

    Peking Univ Dept Breast Surg Shenzhen Hosp Shenzhen 518036 Guangdong Peoples R China;

    Peking Univ Dept Breast Surg Shenzhen Hosp Shenzhen 518036 Guangdong Peoples R China;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 基础医学;
  • 关键词

    breast cancer; anastrozole; testosterone undecanoate; androgen receptor;

    机译:乳腺癌;Anastrozole;睾酮未成熟;雄激素受体;

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