TFEB
自噬
溶酶体
PI3K/AKT/mTOR通路
细胞毒性T细胞
结直肠癌
细胞生物学
化学
雷帕霉素的作用靶点
癌症研究
程序性细胞死亡
ATG5型
癌细胞
癌症
生物
细胞凋亡
细胞内
细胞生长
mTORC1型
信号转导
自噬体
细胞
细胞毒性
生物化学
遗传学
体外
酶
作者
Y. Zhou,Xingtao Zhou,Xiao‐Jun Huang,Tao Hong,Ke Zhang,Wucheng Qi,Meijun Guo,Shaoping Nie
标识
DOI:10.1021/acs.jafc.0c07166
摘要
Targeting autophagy and lysosome may serve as a promising strategy for cancer therapy. Tea polysaccharide (TP) has shown promising antitumor effects. However, its mechanism remains elusive. Here, TP was found to have a significant inhibitory effect on the proliferation of colon cancer line HCT116 cells. RNA-seq analysis showed that TP upregulated autophagy and lysosome signal pathways, which was further confirmed through experiments. Immunofluorescence experiments indicated that TP activated transcription factor EB (TFEB), a key nuclear transcription factor modulating autophagy and lysosome biogenesis. In addition, TP inhibited the activity of mTOR, while it increased the expression of Lamp1. Furthermore, TP ameliorated the lysosomal damage and autophagy flux barrier caused by Baf A1 (lysosome inhibitor). Hence, our data suggested that TP repressed the proliferation of HCT116 cells by targeting lysosome to induce cytotoxic autophagy, which might be achieved through mTOR-TFEB signaling. In summary, TP may be used as a potential drug to overcome colon cancer.
科研通智能强力驱动
Strongly Powered by AbleSci AI