Pu Yansong, Zhang Tao, Wang Jianhua, Mao Zhijun, Duan Baojun, Long Yanbin, Xue Fei, Liu Dong, Liu Sida, Gao Zengzhan
The Second Department of General Surgery, Shaanxi Provincial People's Hospital, Xi'an, Shaanxi 710068, P.R. China.
Department of Oncology, Shaanxi Provincial People's Hospital, Xi'an, Shaanxi 710068, P.R. China.
J Cancer. 2018 Sep 8;9(20):3669-3675. doi: 10.7150/jca.27183. eCollection 2018.
Accumulating studies confirmed that luteolin, a common dietary flavonoid which is widely distributed in plants and has diverse beneficial biological function, including anti-oxidant, anti-inflammation and anticancer properties. However, the detail mechanisms of luteolin on GC are poorly understood. Here, we investigated the anticancer effect of luteolin in GC cells and . Luteolin reduced the cell viability in a time and dose-dependent manner. Luteolin significantly inhibited cell cycle progress, colony formation, proliferation, migration, invasion and promoted apoptosis and . Luteolin also regulated these biological effects associated regulators. Mechanically, luteolin treatment regulated Notch1, PI3K, AKT, mTOR, ERK, STAT3 and P38 signaling pathways and modulated a series of miRNAs expression. These findings provide novel insight into the molecular function of luteolin which suggest its potential as a therapeutic agent for human GC.
越来越多的研究证实,木犀草素是一种常见的膳食黄酮类化合物,广泛分布于植物中,具有多种有益的生物学功能,包括抗氧化、抗炎和抗癌特性。然而,木犀草素对胃癌作用的具体机制尚不清楚。在此,我们研究了木犀草素对胃癌细胞的抗癌作用。木犀草素以时间和剂量依赖性方式降低细胞活力。木犀草素显著抑制细胞周期进程、集落形成、增殖、迁移、侵袭并促进凋亡。木犀草素还调节这些生物学效应相关的调节因子。机制上,木犀草素处理调节Notch1、PI3K、AKT、mTOR、ERK、STAT3和P38信号通路,并调节一系列miRNA的表达。这些发现为木犀草素的分子功能提供了新的见解,表明其作为人类胃癌治疗药物的潜力。