Yan Weixin, Chen Shouhui, Zhao Yiyang, Ye Xiaoyu
Institute of Robotics, School of Mechanical Engineering, Shanghai Jiao Tong University, Shanghai 200240, P.R. China.
School of Biomedical Engineering, Med-X Research Institute, Shanghai Jiao Tong University, Shanghai 200030, P.R. China.
Oncol Lett. 2018 Jun;15(6):8442-8446. doi: 10.3892/ol.2018.8388. Epub 2018 Mar 29.
The present study aimed to investigate the effect of fisetin on proliferation and apoptosis of gastric cancer cells, as well as the underlying mechanism. Proliferation in SGC7901 cancer and GES-1 normal cells was analyzed using a CCK-8 assay. Apoptosis was analyzed using an Annexin V/Propidium Iodide apoptosis kit and phosphorylation of extracellular signal-regulated kinase (ERK) 1/2 was analyzed by western blot assay. Treatment of SGC7901 cells with various concentrations (1, 5, 10, 15 and 20 µM) of fisetin for 48 h resulted in a concentration dependent reduction in proliferation. Flow cytometry revealed a marked increase in apoptosis from 5 µM concentration of fisetin after 48 h. The percentage of apoptotic cells increased to 87% following treatment with 15 µM fisetin for 48 h, compared with 2% in control. Treatment of SGC7901 cells with fisetin for 48 h resulted in a reduction in the activation of ERK 1/2 in a concentration-dependent manner. The reduction in activation of ERK 1/2 was significant following treatment with 15 µM fisetin for 48 h. The inhibitory effect of fisetin on activation of ERK 1/2 was further demonstrated using the ERK 1/2 inhibitor, PD98059. The results indicated a significant reduction in the proliferation of SGC7901 cells following treatment with PD98059 (P<0.002). The reduction by PD98059 administration was comparable to that observed following fisetin treatment for 48 h. In conclusion, the current study demonstrates that fisetin inhibits the proliferation of gastric cancer cells and induces apoptosis through suppression of ERK 1/2 activation. Thus, fisetin may have therapeutic applications in the treatment of gastric cancer.
本研究旨在探讨非瑟酮对胃癌细胞增殖和凋亡的影响及其潜在机制。采用CCK-8法分析SGC7901癌细胞和GES-1正常细胞的增殖情况。使用膜联蛋白V/碘化丙啶凋亡试剂盒分析凋亡情况,并通过蛋白质免疫印迹法分析细胞外信号调节激酶(ERK)1/2的磷酸化情况。用不同浓度(1、5、10、15和20 μM)的非瑟酮处理SGC7901细胞48小时,导致增殖呈浓度依赖性降低。流式细胞术显示,48小时后,非瑟酮浓度从5 μM起凋亡显著增加。用15 μM非瑟酮处理48小时后,凋亡细胞百分比增至87%,而对照组为2%。用非瑟酮处理SGC7901细胞4个月,导致ERK 1/2的激活呈浓度依赖性降低。用15 μM非瑟酮处理48小时后,ERK 1/2激活的降低显著。使用ERK 1/2抑制剂PD98059进一步证明了非瑟酮对ERK 1/2激活的抑制作用。结果表明,用PD98059处理后,SGC7901细胞的增殖显著降低(P<0.002)。PD98059给药后的降低与非瑟酮处理48小时后观察到的降低相当。总之,本研究表明,非瑟酮通过抑制ERK 1/2激活来抑制胃癌细胞的增殖并诱导凋亡。因此,非瑟酮可能在胃癌治疗中具有治疗应用价值。