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
相关论文
共 50 条
  • [1] Pectolinarigenin inhibits non-small cell lung cancer progression by regulating the PTEN/PI3K/AKT signaling pathway
    Xu, Fei
    Gao, Xuan
    Pan, Huiyun
    ONCOLOGY REPORTS, 2018, 40 (06) : 3458 - 3468
  • [2] Targeting the PI3K/Akt/mTOR pathway in non-small cell lung cancer (NSCLC)
    Tan, Aaron C.
    THORACIC CANCER, 2020, 11 (03) : 511 - 518
  • [3] Targeting the PI3K/Akt/mTOR pathway in non-small cell lung cancer spheroids
    Vella, Nathan
    Estevao, Diogo
    Cruz, Tania
    Oliveira, Maria Jose
    Fenech, Anthony George
    Magri, Vanessa Petroni
    CANCER RESEARCH, 2024, 84 (07)
  • [4] UBQLN4 promotes the proliferation and invasion of non-small cell lung cancer cell by regulating PI3K/AKT pathway
    He, Li
    Chen, Heng
    Ruan, Bin
    He, Li
    Luo, Ming
    Fu, Yulun
    Zou, Rui
    JOURNAL OF CANCER RESEARCH AND CLINICAL ONCOLOGY, 2024, 150 (07)
  • [5] Dual Inhibition of PI3K/Akt/mTOR Pathway and Role of Autophagy in Non-Small Cell Lung Cancer Cells
    Jeong, Eun-Hui
    Choi, Hyeong Sim
    Lee, Tae-Gul
    Kim, Hye-Ryoun
    Kim, Cheol Hyeon
    TUBERCULOSIS AND RESPIRATORY DISEASES, 2012, 72 (04) : 343 - 351
  • [6] Lentinan mitigates pemetrexed chemoresistance by the PI3K/Akt pathway in non-small cell lung cancer
    Tian, Ping
    Du, Dajun
    Yang, Li
    Zhou, Nan
    Tao, Ling
    CELL BIOCHEMISTRY AND BIOPHYSICS, 2024, 82 (02) : 1421 - 1431
  • [7] KIFC3 promotes the progression of non-small cell lung cancer cells through the PI3K/Akt pathway
    Mu, Yu
    Liu, Haoxiang
    Luo, Anni
    Zhang, Qingxiang
    THORACIC CANCER, 2024, 15 (33) : 2356 - 2364
  • [8] Targeting PI3K/AKT/mTOR pathway in non small cell lung cancer
    Fumarola, Claudia
    Bonelli, Mara A.
    Petronini, Pier Giorgio
    Alfieri, Roberta R.
    BIOCHEMICAL PHARMACOLOGY, 2014, 90 (03) : 197 - 207
  • [9] MiR-29c reduces the cisplatin resistance of non-small cell lung cancer cells by negatively regulating the PI3K/Akt pathway
    Dian-min Sun
    Bu-fu Tang
    Zhen-xiang Li
    Hong-bo Guo
    Jin-ling Cheng
    Ping-ping Song
    Xin Zhao
    Scientific Reports, 8
  • [10] MiR-29c reduces the cisplatin resistance of non-small cell lung cancer cells by negatively regulating the PI3K/Akt pathway
    Sun, Dian-min
    Tang, Bu-fu
    Li, Zhen-xiang
    Guo, Hong-bo
    Cheng, Jin-ling
    Song, Ping-ping
    Zhao, Xin
    SCIENTIFIC REPORTS, 2018, 8