PI3K/AKT/mTOR通路
体内
细胞凋亡
细胞生长
胰腺癌
体外
蛋白激酶B
癌症研究
生长抑制
点头
化学
免疫印迹
MTT法
细胞培养
生物
分子生物学
癌症
生物化学
遗传学
生物技术
基因
作者
Jieming Xie,Congfei Wang,Aiqin Yang,Qian Zhang,Qiang Yin,Heguang Huang,Minghuang Chen
出处
期刊:Anti-cancer Agents in Medicinal Chemistry
[Bentham Science]
日期:2013-06-01
卷期号:13 (6): 952-956
被引量:8
标识
DOI:10.2174/18715206113139990109
摘要
Objective: To investigate the effect of cucurmosin (CUS) on proliferation inhibition in the human pancreatic cancer cell line SW-1990 in vitro and in vivo. Methods: 1. MTT assay was used to analyse the proliferation inhibition of CUS in SW-1990 cells compared with gemcitabine (GEM) in vitro. 2. We established an NOD-SCID mice orthotopic transplantation model and estimated the proliferation inhibition effect of CUS in SW-1990 cells in vivo. 3. Western blot was used to determine the protein expressions of Caspase 3, Bcl-2, Caspase 9, PI3K, Akt, mTOR, P70S6k, and 4E-BP1 after CUS intervention. Results: 1. CUS inhibited the proliferation of pancreatic cancer cells and induced apoptosis in CUS dose- and time-dependent manners. 2. NOD-SCID mice models were established successfully, and the tumour proliferation inhibition rates of these models increased compared with the control group. 3. CUS inhibited all of the examined proteins in the PI3K/Akt/mTOR signalling pathway and induced active fragments of Caspase 3 and Caspase 9. Conclusion: 1. CUS can inhibit the growth of SW-1990 cells in vitro and in vivo. 2. CUS can induce apoptosis in SW-1990 cells to inhibit cell growth. Keywords: Pancreatic cancer, cucurmosin, proliferation inhibition, apoptosis.
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