首页> 外文期刊>Cancer letters >HSP90 inhibitor (NVP-AUY922) enhances the anti-cancer effect of BCL-2 inhibitor (ABT-737) in small cell lung cancer expressing BCL-2
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HSP90 inhibitor (NVP-AUY922) enhances the anti-cancer effect of BCL-2 inhibitor (ABT-737) in small cell lung cancer expressing BCL-2

机译:HSP90抑制剂(NVP-AUY922)增强了BCL-2抑制剂(ABT-737)在表达BCL-2的小细胞肺癌中的抗癌作用

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摘要

Abstract Small cell lung cancer (SCLC) cannot be efficiently controlled using existing chemotherapy and radiotherapy approaches, indicating the need for new therapeutic strategies. Although ABT-737, a B-cell lymphoma-2 (BCL-2) inhibitor, exerts anticancer effects against BCL-2-expressing SCLC, monotherapy with ABT-737 is associated with limited clinical activity because of the development of resistance and toxicity. Here, we examined whether combination therapy with ABT-737 and heat shock protein 90 (HSP90) inhibitor NVP-AUY922 exerted synergistic anticancer effects on SCLC. We found that the combination of ABT-737 and NVP-AUY922 synergistically induced the apoptosis of BCL-2-expressing SCLC cells. NVP-AUY922 downregulated the expression of AKT and ERK, which activate MCL-1 to induce resistance against ABT-737. The synergistic effect was also partly due to blocking NF-κB activation, which induces anti-apoptosis protein expressions. However, interestingly, targeting BCL-2 and MCL-1 or BCL2 and NF-κB did not induce the cytotoxicity. In conclusion, our study showed that combination of BCL2 inhibitor with HSP90 inhibitor increased activity in in?vitro and in?vivo study in only BCL-2 expressing SCLC compared to either single BCL2 inhibitor or HSP inhibitor. The enhanced activity might be led by blocking several apoptotic pathways simultaneously rather than a specific pathway.
机译:摘要使用现有的化疗和放射疗法方法无法有效地控制小细胞肺癌(SCLC),表明需要新的治疗策略。虽然ABT-737,B细胞淋巴瘤-2(BCL-2)抑制剂,对BCL-2表达的SCLC发挥抗癌作用,但由于抗性和毒性的发展,与ABT-737的单疗法与有限的临床活动相关。在这里,我们检查了ABT-737和热休克蛋白90(HSP90)抑制剂NVP-Auy922对SCLC的协同抗癌作用。我们发现ABT-737和NVP-AUY922的组合协同诱导了Bcl-2表达SCLC细胞的凋亡。 NVP-AUY922下调AKT和ERK的表达,激活MCL-1以诱导ABT-737的抗性。协同效应也部分是由于阻断NF-κB活化,这诱导抗凋亡蛋白表达。然而,有趣的是,靶向BCL-2和MCL-1或BCL2和NF-κB没有诱导细胞毒性。总之,我们的研究表明,与单一BCL2抑制剂或HSP抑制剂相比,BCL2抑制剂与HSP90抑制剂的组合在β体外和β体外研究中的活性。可以通过同时阻断若干凋亡途径而不是特定途径来引入增强的活性。

著录项

  • 来源
    《Cancer letters》 |2017年第2017期|共8页
  • 作者单位

    Biomedical Science and Engineering Interdisciplinary Program Korea Advanced Institute of Science;

    Department of Oncology University of Ulsan College of Medicine Asan Medical Center;

    Biomedical Science and Engineering Interdisciplinary Program Korea Advanced Institute of Science;

    Department of Oncology University of Ulsan College of Medicine Asan Medical Center;

    Department of Oncology University of Ulsan College of Medicine Asan Medical Center;

    Department of Oncology University of Ulsan College of Medicine Asan Medical Center;

    Department of Oncology University of Ulsan College of Medicine Asan Medical Center;

    Biomedical Science and Engineering Interdisciplinary Program Korea Advanced Institute of Science;

    Department of Oncology University of Ulsan College of Medicine Asan Medical Center;

    Department of Oncology University of Ulsan College of Medicine Asan Medical Center;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 肿瘤学;
  • 关键词

    Small cell lung cancer; BCL-2 inhibitor; HSP90 inhibitor; Combination therapy;

    机译:小细胞肺癌;BCL-2抑制剂;HSP90抑制剂;联合治疗;

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