a Department of Hematology , Affiliated Rui-Jin Hospital of Shanghai Jiao-Tong University School of Medicine , Shanghai , China.
b Hongqiao International Institute of Medicine, Shanghai Tongren Hospital; Key Laboratory of Cell Differentiation and Apoptosis of the Chinese Ministry of Education , Shanghai Jiao Tong University School of Medicine , Shanghai , China.
Cancer Biol Ther. 2019;20(3):381-390. doi: 10.1080/15384047.2018.1529112. Epub 2018 Oct 25.
Montelukast is an anti-asthmatic medication, and has recently showed its inhibitory effects on the proliferation of cancers. The purpose of this study was to identify the cytotoxic effects of montelukast on multiple myeloma (MM) cells and the combination effects of montelukast and carfilzomib in the treatment of MM. Results revealed that montelukast induced a dose- and time-dependent cytotoxicity in MM cells lines and significantly suppressed the colony formation of myeloma cells. Furthermore, montelukast enhanced the cytotoxicity of carfilzomib in MM cell lines. This anti-tumor effect was associated with decreased c-Myc via the inhibition of mTOR signaling pathway. Moreover, the combination of montelukast and carfilzomib induced apoptosis of myeloma cells effectively, even in the presence of bone marrow stromal cells (BMSCs). It is more important to note that the co-treatment exhibited similar cytocidal effects in carfilzomib-resistant cell lines (U266R and 8226R). In addition, the combined effects were noted in two MM xenograft mice models and 7 cases of human CD138 myeloma cells (4 newly diagnosed cases and 3 relapsed cases) with no cytotoxicity on peripheral blood mononuclear cells (PBMCs) from 5 healthy donors. Our data suggested that montelukast enhanced the cytotoxicity of carfilzomib in both carfilzomib-sensitive and carfilzomib-resistant MM cell lines. These findings may facilitate the development of therapeutic strategies and provide a promising therapeutic combination regimen for the treatment of refractory myeloma.
孟鲁司特是一种抗哮喘药物,最近显示其对癌症增殖具有抑制作用。本研究旨在确定孟鲁司特对多发性骨髓瘤(MM)细胞的细胞毒性作用,以及孟鲁司特和卡非佐米联合治疗 MM 的协同作用。结果表明,孟鲁司特在 MM 细胞系中诱导了剂量和时间依赖性的细胞毒性,显著抑制了骨髓瘤细胞的集落形成。此外,孟鲁司特增强了卡非佐米在 MM 细胞系中的细胞毒性。这种抗肿瘤作用与通过抑制 mTOR 信号通路导致 c-Myc 减少有关。此外,孟鲁司特和卡非佐米的联合治疗可有效诱导骨髓瘤细胞凋亡,即使存在骨髓基质细胞(BMSCs)也是如此。更重要的是,在卡非佐米耐药细胞系(U266R 和 8226R)中,联合治疗也显示出相似的细胞杀伤作用。此外,在两种 MM 异种移植小鼠模型和 7 例人 CD138 骨髓瘤细胞(4 例新诊断病例和 3 例复发病例)中观察到联合作用,对 5 例健康供体的外周血单个核细胞(PBMCs)无细胞毒性。我们的数据表明,孟鲁司特增强了卡非佐米在卡非佐米敏感和卡非佐米耐药 MM 细胞系中的细胞毒性。这些发现可能有助于开发治疗策略,并为治疗难治性骨髓瘤提供一种有前途的联合治疗方案。