PI3K/AKT/mTOR通路
蛋白激酶B
原癌基因酪氨酸蛋白激酶Src
小桶
细胞凋亡
机制(生物学)
癌症研究
生物
信号转导
化学
癌细胞
癌症
细胞生物学
生物化学
基因表达
转录组
基因
遗传学
认识论
哲学
作者
Xinye Wang,Yujue Wang,Zi‐Lin Hou,Bowen Guo,Ru-Qi Wang,Qingbo Liu,Guo‐Dong Yao,Shao‐Jiang Song
标识
DOI:10.1080/14786419.2023.2247536
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.
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