自噬
PI3K/AKT/mTOR通路
蛋白激酶B
结直肠癌
癌症研究
细胞生长
体内
激酶
癌症
程序性细胞死亡
细胞生物学
体外
细胞凋亡
生物
信号转导
化学
生物化学
遗传学
作者
Sha Huang,Luping Lin,Yifei Ma,Qing Zhu,Ningna Weng
标识
DOI:10.1016/j.ejphar.2023.176091
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.
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