虫草素
细胞凋亡
A549电池
细胞周期
顺铂
细胞生物学
半胱氨酸蛋白酶
癌细胞
化学
细胞生长
活力测定
癌症研究
生物
程序性细胞死亡
癌症
生物化学
化疗
遗传学
作者
Seong Hyeok Cho,In‐Cheol Kang
标识
DOI:10.1016/j.bbrc.2018.02.188
摘要
The goal of this study is to determine the anti-cancer mechanism of Cordycepin in A549 Cisplatin-Resistance (CR) lung cancer cells. Cordycepin inhibited the viability of A549CR cells in a dose-dependent manner. The cell inhibition was due to induction of apoptosis in the cells treated with Cordycepin by activation of caspase -3, -8 and -9 activities. The cell cycle analysis showed that accumulation of Sub G1 was observed in Cordycepin-treated with A549CR lung cancer cells. Based on the data of expression profile analysis of cell signaling proteins using IPS-FPAA, H-Ras was down-regulated in Cordycepin-treated A549CR cells. Collectively, anti-proliferative function of Cordycepin was due to stimulation of the cell apoptosis and the cell cycle arrest via caspases activation and down-regulation of H-Ras.
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