School of Pharmaceutical Sciences, Zhengzhou University, Zhengzhou, 450001, China.
School of Pharmaceutical Sciences, Zhengzhou University, Zhengzhou, 450001, China; State Key Laboratory of Pharmaceutical Biotechnology, Nanjing University, Nanjing, 210023, Jiangsu, China.
Eur J Med Chem. 2019 Jul 15;174:76-86. doi: 10.1016/j.ejmech.2019.04.044. Epub 2019 Apr 17.
Reactive oxygen species (ROS) play crucial roles in maintaining redox balance and regulating physiological processes, ROS levels in cancer cells are relatively higher than those in normal cells. Therefore, elevating cellular ROS levels may be a viable strategy for selective killing of cancer cells. In this work, we synthesized a series of new theobromine derivatives and evaluated their cytotoxicity against gastric cancer cells MGC-803, SGC-7901 and HGC-27. Particularly, MQS-14 potently inhibited cell growth of MGC-803, SGC-7901 and HGC-27 cells at low micromolar levels. Mechanistic studies showed that compound MQS-14 decreased cell viability of MGC-803 cells and inhibited cell division revealed by the CFDA and EdU staining assays. MQS-14 increased cellular ROS levels and activated the MAPK pathway accompanied by the decreased p-ERK and increased p-JNK expression. MQS-14 also induced DNA damage and apoptosis in MGC-803 cells. To conclude, MQS-14 induced cell death of MGC-803 cells partly through elevating cellular ROS levels.
活性氧(ROS)在维持氧化还原平衡和调节生理过程中发挥着关键作用,癌细胞中的 ROS 水平相对高于正常细胞。因此,提高细胞内 ROS 水平可能是选择性杀伤癌细胞的一种可行策略。在这项工作中,我们合成了一系列新的可可碱衍生物,并评估了它们对胃癌细胞 MGC-803、SGC-7901 和 HGC-27 的细胞毒性。特别是,MQS-14 在低微摩尔水平下强烈抑制 MGC-803、SGC-7901 和 HGC-27 细胞的生长。机制研究表明,化合物 MQS-14 通过 CFDA 和 EdU 染色试验降低 MGC-803 细胞的活力并抑制细胞分裂。MQS-14 增加了细胞内 ROS 水平,并激活了 MAPK 途径,伴随着 p-ERK 的减少和 p-JNK 的增加。MQS-14 还诱导了 MGC-803 细胞的 DNA 损伤和凋亡。总之,MQS-14 通过提高细胞内 ROS 水平诱导了 MGC-803 细胞的死亡。