Ingenane-type diterpenoids inhibit non-small cell lung cancer cells by regulating SRC/PI3K/Akt pathway

被引:4
作者
Wang, Xin-Ye [1 ]
Wang, Yu-Jue [1 ]
Hou, Zi-Lin [1 ]
Guo, Bo-Wen [1 ]
Wang, Ru-Qi [1 ]
Liu, Qingbo [1 ]
Yao, Guo-Dong [1 ]
Song, Shao-Jiang [1 ]
机构
[1] Shenyang Pharmaceut Univ, Engn Res Ctr Nat Med Act Mol Res & Dev, Key Lab Computat Chem Based Nat Antitumor Drug Res, Key Lab Nat Bioact Cpds Discovery & Modificat,Sch, Shenyang 110016, Liaoning, Peoples R China
关键词
Non-small cell lung cancer; ingenane-type diterpenoids; 13-oxyingenol-dodecanoate; SRC/PI3K/akt pathway; NATURAL-PRODUCTS; PI3K/AKT/MTOR PATHWAY; APOPTOSIS; SUPPRESSION; DISCOVERY; AKT;
D O I
10.1080/14786419.2023.2247536
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Ingenane-type diterpenoids (ITDs) are distinct components of plants belonging to the genus Euphorbia. These compounds have significant cytotoxic effects on non-small cell lung cancer (NSCLC) cells. However, the underlying molecular mechanism has yet to be reported. To explore the mechanism of the anticancer effect of ITDs, we carried out a network pharmacology prediction study. PPI network suggested that SRC and PI3K had high levels of interaction. In addition, KEGG analysis revealed that these common targets were significantly enriched in the PI3K/Akt signalling pathway. 13-oxyingenol-dodecanoate (13OD) was used for validation after the biological evaluation of some ITDs against NSCLC cells. It demonstrated that 13OD could significantly inhibit the growth of NSCLC cells by inducing apoptosis. The results from molecular docking and Western blotting showed that 13OD interacted with SRC and PI3K and down-regulated the SRC/PI3K/Akt signalling pathway in NSCLC cells. This study provided the underlying mechanism of ITDs against NSCLC. [GRAPHICS] .
引用
收藏
页码:3460 / 3465
页数:6
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