Scoparone induces autophagic cell death via the PAK1/AKT axis in colorectal cancer

被引:3
|
作者
Huang, Sha [1 ,2 ,4 ]
Lin, Luping [1 ,2 ,4 ]
Ma, Yifei
Zhu, Qing [3 ]
Weng, Ningna [1 ,2 ,3 ]
机构
[1] Fujian Med Univ, Fujian Canc Hosp, Dept Med Oncol, Clin Oncol Sch, Fuzhou 350011, Fujian, Peoples R China
[2] Fujian Med Univ, Fujian Canc Hosp, Innovat Ctr Canc Res, Clin Oncol Sch, Fuzhou 350011, Peoples R China
[3] Sichuan Univ, Dept Abdominal Oncol, West China Hosp, Chengdu 610041, Peoples R China
[4] Fujian Med Univ, Fujian Canc Hosp, Fujian Key Lab Adv Technol Canc Screening & Early, Clin Oncol Sch, Fuzhou 350011, Fujian, Peoples R China
关键词
Scoparone; Colorectal cancer; Autophagy; PAK1; AKT; RESISTANCE; CHEMOTHERAPY; TAMOXIFEN; PAK;
D O I
10.1016/j.ejphar.2023.176091
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Colorectal cancer (CRC) is one of most common malignancies worldwide, yet curative therapy remains a clinical challenge. Here, we demonstrate that scoparone (Scop), a traditional Chinese medicine monomer, inhibits the growth of CRC cells both in vitro and in vivo. Further studies found that Scop treatment induces complete autophagic flux in CRC cells, while inhibition of autophagy markedly represses the antiproliferative activities of Scop, suggesting an antitumour property of Scop-induced autophagy in CRC. Mechanistically, Scop induced autophagy initiation by reducing P21-activated kinase 1 (PAK1) expression and subsequently repressing the AKT/mTOR signaling pathway. Collectively, our study suggests that Scop is a potential anti-CRC therapeutic option and provides an underlying molecular mechanism for its antitumour effect in CRC.
引用
收藏
页数:9
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