球体
细胞因子
血管生成
人口
药品
药理学
癌症研究
免疫学
肿瘤科
医学
生物
体外
生物化学
环境卫生
作者
Mengqi Liu,Yihe Wang,Chao Wang,Ping Li,Jiaoyan Qiu,Ningkai Yang,Mingyuan Sun,Lin Han
标识
DOI:10.1002/adhm.202402321
摘要
Angiogenesis is a key player in drug resistance to targeted therapies for breast cancer. The average expression of angiogenesis-related cytokines is widely associated with the treatments of target therapies for a population of cells or spheroids, overlooking the distinct responses for individuals. In this work, a highly integrated microfluidic platform is developed for the generation of monodisperse multicellular tumor spheroids (MTSs), drug treatments, and the measurement of cytokines for individual MTSs in a single chip. The platform allows the correlation evaluation between cytokine secretion and drug treatment at the level of individual spheroids. For validation, quantities of six representative proangiogenic cytokines are tested against treatments with four model drugs at varying times and concentrations. By applying a linear regression model, significant correlations are established between cytokine secretion and the treated drug concentration for individual spheroids. The proposed platform provides a high-throughput method for the investigation of the molecular mechanism of the cytokine response to targeted therapies and paves the way for future drug screening using predictive regression models at the single-spheroid level.
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