Daptomycin Inhibits Multiple Myeloma Progression through Downregulating the Expression of RPS19

流式细胞术 硼替佐米 细胞凋亡 细胞周期 细胞生长 多发性骨髓瘤 细胞培养 癌症研究 细胞计数 化学 细胞 分子生物学 生物 免疫学 生物化学 遗传学
作者
Yijun Zhuang,Yin Zhang,Caiyun Chen,Jincheng Chen,Qiuxia Xu,Peihong Wang
出处
期刊:Combinatorial Chemistry & High Throughput Screening [Bentham Science Publishers]
卷期号:27
标识
DOI:10.2174/0113862073283460240129104114
摘要

Objectives:: This study aimed to explore new therapeutic drugs for multiple myeloma (MM). MM is a common plasma cell malignant proliferative disease, accounting for 15% of hematological malignancies. The role of daptomycin (DAP), a potential anti-tumor drug, remains unclear in MM. In the present research, we investigated the anticancer effect of DAP in MM cell line RPMI 8226. Methods:: RPMI 8226 cells were treated with DAP (20 μM, 40 μM, and 80 μM) with 20 nM bortezomib (BZ) as a positive control. Cell function was detected using CCK8, flow cytometry, and transwell assay. objective: In the present research, we investigated the anticancer effect of DAP in MM cell line RPMI 8226. Results:: In MM cells, DAP inhibited proliferation and induced apoptosis. The cell cycle was arrested at the G1 phase after the treatment of DAP. The migration and invasion abilities were also inhibited by DAP treatment in RPMI 8226 cells. Importantly, the mRNA and protein levels of RPS19 were downregulated in DAP-treated RPMI 8226 cells. method: RPMI 8226 cells were treated with DAP (20 μM, 40 μM and 80 μM) with 20 nM bortezomib (BZ) as a positive control. Cell function was detected using CCK8, flow cytometry and transwell assay. Conclusion:: DAP inhibited the proliferation, migration, and invasion and promoted the apoptosis of MM cells. Mechanistically, the RPS19 expression was significantly decreased in DAPtreated cells. This research provides a potential therapeutic drug for MM therapy.
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