Xu Bin, Tao Ze-Zhang
Department of Oncology, Wuhan University Renmin Hospital, Wuhan, Hubei, P.R. China.
Oncol Res. 2014;22(4):213-217. doi: 10.3727/096504015X14386062091398.
To enhance the anticancer efficacy of gemcitabine in the treatment of non-small cell lung cancer (NSCLC), the potential synergistic effect of piceatannol on gemcitabine cytotoxicity was investigated in the human NSCLC A459 cell line. The MTT cell viability assay showed that piceatannol significantly enhanced the cytotoxic effects of gemcitabine by lowering the gemcitabine IC50 value. Flow cytometry analysis revealed that piceatannol exerted its pharmacological effect mainly by increasing the late apoptotic population. Western blot analysis showed that gemcitabine induced the expression of the proapoptotic proteins Bad and Bak, and pretreatment with piceatannol further increased Bak expression, leading to an increased number of cells undergoing late apoptosis. The findings from this study show that piceatannol can enhance the cytotoxic effects of gemcitabine by enhancing expression of the proapoptotic protein Bak, thereby providing the rational basis for a novel combination strategy for the treatment of NSCLC.
为提高吉西他滨治疗非小细胞肺癌(NSCLC)的抗癌疗效,在人NSCLC A459细胞系中研究了白皮杉醇对吉西他滨细胞毒性的潜在协同作用。MTT细胞活力测定表明,白皮杉醇通过降低吉西他滨IC50值显著增强了吉西他滨的细胞毒性作用。流式细胞术分析显示,白皮杉醇主要通过增加晚期凋亡细胞群发挥其药理作用。蛋白质免疫印迹分析表明,吉西他滨诱导促凋亡蛋白Bad和Bak的表达,用白皮杉醇预处理可进一步增加Bak的表达,导致晚期凋亡细胞数量增加。本研究结果表明,白皮杉醇可通过增强促凋亡蛋白Bak的表达来增强吉西他滨的细胞毒性作用,从而为NSCLC治疗的新型联合策略提供理论依据。