Division of Pharmacology, Department of Preclinical Science, Faculty of Medicine, Thammasat University, Pathumthani, 12120, Thailand.
Division of Anatomy, Department of Preclinical Science, Faculty of Medicine, Thammasat University, Pathumthani, 12120, Thailand.
Asian Pac J Cancer Prev. 2021 Dec 1;22(12):4001-4009. doi: 10.31557/APJCP.2021.22.12.4001.
The combination treatment is a way to improve the therapeutic strategy of temozolomide (TMZ) -resistant glioblastoma (GBM). Taurine (TAU) has the potential to inhibit growth in various cancer cells. The aim of this study was to examine the combined effects of TMZ and TAU on cultured human GBM, U-251 MG cells.
The cells were incubated with TMZ, TAU, and the combination of both in various ratios. MTT assay was performed to measure the cell viability of the treatments and then the synergistic interactions were evaluated by the Chou-Talalay method. The cell cycle and apoptotic properties of the combined treatment on U-251 MG cells were examined by flow cytometry. The Hoechst 33342 stainings were applied to visualize the morphologic change in the apoptotic process.
The combined treatment with a dose reduction of each expressed synergistic effect on the decrease of cell viability. The study on the cell cycle resulted in G2/M phase arrest with increasing apoptotic cells in the SubG1 phase. Moreover, the apoptotic effects of the combinations on U-251 MG cells were explained by the increase of apoptotic cells in both early and late stages and illustrated by some characteristics of the apoptotic process including condensed chromatin and fragmented nuclei.
The study showed that the combination between TMZ and TAU has a potential in anticancer properties against U-251 MG manifested by the induction of G2/M arrest and apoptosis. These results suggest that this combination may be useful to enhance the efficacy and reduce some adverse events of GBM treatment in the future.
联合治疗是改善替莫唑胺(TMZ)耐药胶质母细胞瘤(GBM)治疗策略的一种方法。牛磺酸(TAU)具有抑制多种癌细胞生长的潜力。本研究旨在研究 TMZ 和 TAU 联合作用对培养的人 GBM、U-251 MG 细胞的影响。
将细胞与 TMZ、TAU 以及两者的不同比例组合孵育。采用 MTT 法检测细胞活力,然后采用 Chou-Talalay 法评估协同作用。通过流式细胞术检测联合处理对 U-251 MG 细胞周期和凋亡特性的影响。采用 Hoechst 33342 染色观察凋亡过程中的形态变化。
联合治疗剂量降低,对细胞活力下降表现出协同作用。细胞周期研究导致 G2/M 期阻滞,SubG1 期凋亡细胞增加。此外,联合治疗对 U-251 MG 细胞的凋亡作用通过早期和晚期凋亡细胞的增加得到了解释,并通过凋亡过程的一些特征来阐明,包括染色质浓缩和核碎裂。
本研究表明,TMZ 和 TAU 联合具有抗癌特性,可诱导 G2/M 期阻滞和凋亡,对 U-251 MG 有潜在作用。这些结果表明,这种联合治疗可能有助于提高 GBM 治疗的疗效,并减少未来的一些不良反应。