球体
熊果酸
微流控
细胞
三维细胞培养
癌症
化学
细胞培养
体外
微流控芯片
药品
癌细胞
癌症研究
药物输送
纳米技术
生物医学工程
生物
材料科学
医学
药理学
生物化学
色谱法
内科学
遗传学
作者
Shiqi Chang,Jing Wen,Yue Su,Huipeng Ma
出处
期刊:Electrophoresis
[Wiley]
日期:2022-03-22
卷期号:43 (13-14): 1466-1475
被引量:4
标识
DOI:10.1002/elps.202100382
摘要
Abstract At present, the probability that a new anti‐tumor drug will eventually succeed in clinical trials is extremely low. In order to make up for this shortcoming, the use of a three‐dimensional (3D) cell culture model for secondary screening is often necessary. Cell spheroid is the easiest 3D model tool for drug screening. In this study, the microfluidic chip with a microwell array was manufactured, which could allow the formation of tumor spheroids with uniform size and easily retrieve cell spheroids from the chip. Cell spheroids were successfully cultured for over 15 days and the survival rate was as high as 80%. Subsequently, cellular response to the ursolic acid (UA) was observed on the chip. Compared to the monolayer culture cells in vitro , the tumor spheroids showed minor levels of epithelial‐mesenchymal transition fluctuation after drug treatment. The mechanism of cell spheroid resistance to UA was further verified by detecting the expression level of upstream pathway proteins. But the invasive ability of tumor spheroids was attenuated when the duration of action of UA extended. The anti‐cancer effect of UA was innovatively evaluated on breast cancer by using the microfluidic device, which could provide a basis and direction for future preclinical research on UA.
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