Xu Wei, Ma Wei-Wei, Zeng Hui-Hui
State Key Laboratory of Natural and Biomimetic Drugs, Peking University, Beijing, China E-mail :
Asian Pac J Cancer Prev. 2014;15(17):7129-35. doi: 10.7314/apjcp.2014.15.17.7129.
In this study, we aimed to evaluate the growth inhibitory effect of the combination of ethaselen (BBSKE) and low fixed dose of selenite against A549 human non-small cell lung cancer cells in vitro.
Growth inhibitory effects against A549 cells were determined by SRB assay. Combination index (CI) values were calculated based on Chou-Talalay median-effect analyses. Dose reduction index (DRI) values were applied to calculate dose reduction of selenite. Contents of free thiols and GSH were determined by DTNB assay and intracellular ROS levels by DCFH-DA fluorescence labeling.
Compared with BBSKE or selenite single treatment, the combined application of ethaselen and a low fixed dose of selenite shortened the onset time of sodium selenite, reduced IC50 values, and increased the maximum inhibition rates, suggesting a possible molecular mechanism of the synergism. Obvious synergistic effects were observed after different times of combination treatment, especially after 24 h. Compared with selenite single treatment, dosage of selenite could be remarkably reduced in combination therapy to gain the same inhibitory effect on cell proliferation. Compared with BBSKE single treatment, the content of free thiols and GSH were significantly reduced and ROS levels greatly elevated in the combination group. For the combination treatment, cell viability increased as greater concentrations of GSH were added.
All these results indicate that the combination treatment of BBSKE and selenite showed synergism to inhibit A549 cell proliferation in vitro, and also reduced the selenite dosage to mitigate its toxicity which is very meaningful for combination chemotherapy of lung cancer. The synergism was probably caused by the accelerated exhaustion of intracellular reductive substances, such as free thiols and GSH, which ultimately leads to enhanced oxidative stress and apoptosis.
在本研究中,我们旨在评估乙磺半胱氨酸(BBSKE)与低固定剂量亚硒酸盐联合应用对体外培养的A549人非小细胞肺癌细胞的生长抑制作用。
采用SRB法测定对A549细胞的生长抑制作用。根据Chou-Talalay中位效应分析计算联合指数(CI)值。应用剂量降低指数(DRI)值计算亚硒酸盐的剂量降低情况。采用DTNB法测定游离巯基和谷胱甘肽(GSH)含量,用DCFH-DA荧光标记法测定细胞内活性氧(ROS)水平。
与BBSKE或亚硒酸盐单药治疗相比,乙磺半胱氨酸与低固定剂量亚硒酸盐联合应用缩短了亚硒酸钠的起效时间,降低了IC50值,提高了最大抑制率,提示可能存在协同作用的分子机制。联合治疗不同时间后均观察到明显的协同效应,尤其是24小时后。与亚硒酸盐单药治疗相比,联合治疗可显著降低亚硒酸盐剂量以获得相同的细胞增殖抑制效果。与BBSKE单药治疗相比,联合组游离巯基和GSH含量显著降低,ROS水平显著升高。对于联合治疗,随着加入的GSH浓度增加,细胞活力增加。
所有这些结果表明,BBSKE与亚硒酸盐联合治疗在体外显示出协同抑制A549细胞增殖的作用,同时降低了亚硒酸盐剂量以减轻其毒性,这对于肺癌联合化疗具有重要意义。协同作用可能是由于细胞内还原性物质如游离巯基和GSH的加速耗竭,最终导致氧化应激增强和细胞凋亡。