Department of Medical Biology, Medical Faculty, Ege University, Bornova, 35100, Izmir, Turkey.
Department of Stem Cell, Health Science Institute, Ege University, Bornova, 35100, Izmir, Turkey.
Anticancer Agents Med Chem. 2020;20(18):2267-2273. doi: 10.2174/1871520620666200721121517.
Salinomycin, an ionophore antibiotic, is known to be an effective agent in reducing the viability of Glioblastoma (GBM) cells. The combination of salinomycin with other chemotherapeutic drugs would help to overcome the drug resistance of GBM cells.
This study aims to test the combinatorial effect of salinomycin and AZD3463 in T98G GBM cells.
The cytotoxic effects of drugs on T98G GBM cells were determined by using WST-8 assay. Flow cytometry was used to identify apoptosis and cell cycle profiles after treatments. Real-time PCR was used to portray mRNA expression profiles of genes in the Wnt-signaling pathway after treatments.
IC50 concentrations of AZD3463 and salinomycin were 529nM and 7.3μM for 48h, respectively. The combination concentrations of AZD3463 and salinomycin were 3.3μM and 333nM, respectively. The combination treatment showed a synergistic effect on reducing the viability of GBM cells. AZD3463, salinomycin, and their combination induced apoptosis in 1.2, 1.4, and 3.2 folds, respectively. AZD3463 and the combination treatment induced the cell cycle arrest at the G1 phase. Salinomycin and AZD3463 treatments, either alone or in combination, resulted in the downregulation or upregulation of mRNA expression levels of genes in the Wntsignaling pathway.
Salinomycin, AZD3463, and their combination may inhibit proliferation and induce apoptosis in GBM cells due to a decrease in expression levels of genes acting in both the canonical and non-canonical Wnt signaling pathways. The Wnt signaling pathway may be involved in salinomycin-AZD3463 drug interaction.
莫能菌素是一种离子载体抗生素,已知能有效降低神经胶质瘤(GBM)细胞的活力。莫能菌素与其他化疗药物联合使用有助于克服 GBM 细胞的耐药性。
本研究旨在检测莫能菌素和 AZD3463 联合作用于 T98G GBM 细胞的效果。
采用 WST-8 法检测药物对 T98G GBM 细胞的细胞毒性作用。采用流式细胞术检测处理后细胞凋亡和细胞周期谱。采用实时 PCR 检测处理后 Wnt 信号通路基因的 mRNA 表达谱。
AZD3463 和莫能菌素的 IC50 浓度分别为 48h 时的 529nM 和 7.3μM。AZD3463 和莫能菌素的联合浓度分别为 3.3μM 和 333nM。联合处理对降低 GBM 细胞活力表现出协同作用。AZD3463、莫能菌素和联合处理分别诱导细胞凋亡 1.2、1.4 和 3.2 倍。AZD3463 和联合处理诱导细胞周期阻滞在 G1 期。莫能菌素、AZD3463 及其联合处理均导致 Wnt 信号通路中基因的 mRNA 表达水平下调或上调。
莫能菌素、AZD3463 及其联合用药可能通过下调经典和非经典 Wnt 信号通路中基因的表达水平,抑制 GBM 细胞的增殖并诱导其凋亡。Wnt 信号通路可能参与莫能菌素-AZD3463 药物相互作用。