Wnt信号通路
蛋白激酶B
癌症研究
PI3K/AKT/mTOR通路
癌变
AKT1型
信号转导
细胞凋亡
葛兰素史克-3
连环素
结直肠癌
激酶
化学
调节器
癌症
生物
医学
细胞生物学
内科学
生物化学
基因
作者
Shelly Jain,Preety Ghanghas,Chandan Rana,Sankar Nath Sanyal
标识
DOI:10.1080/07357907.2017.1337783
摘要
Non-steroidal anti-inflammatory drugs (NSAIDs) are emerging as novel chemopreventive agents because of their ability in blocking cellular proliferation, and thereby tumor development, and also by promoting apoptosis. GSK-3β, a serine threonine kinase and a negative regulator of the oncogenic Wnt/β-catenin signaling pathway, plays a critical role in the regulation of oncogenesis. Celecoxib and etoricoxib, the two cyclooxygenase-2 (COX-2) selective NSAIDs, and Diclofenac, a preferential COX-2 inhibitory NSAID, had shown uniformly the chemopreventive and anti-neoplastic effects in the early stage of colon cancer by promoting apoptosis as well as an over-expression of GSK-3β while down-regulating the PI3-K/Akt oncogenic pathway.
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