Integrated Microfluidic Platform with Multiple Functions To Probe Tumor-Endothelial Cell Interaction

被引:49
作者
Lin, Ling [1 ,3 ]
Lin, Xuexia [2 ,4 ]
Lin, Luyao [2 ]
Feng, Qiang [1 ,3 ]
Kitamori, Takehiko [5 ]
Lin, Jin-Ming [2 ]
Sun, Jiashu [1 ,3 ]
机构
[1] Natl Ctr Nanosci & Technol, CAS Ctr Excellence Nanosci, CAS Key Lab Standardizat & Measurement Nanotechno, Beijing 100190, Peoples R China
[2] Tsinghua Univ, Beijing Key Lab Microanalyt Methods & Instrumenta, Dept Chem, Key Lab Bioorgan Phosphorus Chem & Chem Biol, Beijing 100084, Peoples R China
[3] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
[4] Huaqiao Univ, Coll Chem Engn, Xiamen 361021, Peoples R China
[5] Univ Tokyo, Sch Engn, Dept Appl Chem, Bunkyo Ku, 7-3-1 Hongo, Tokyo 1138656, Japan
基金
中国国家自然科学基金;
关键词
MASS-SPECTROMETRY; DEVICE; VEGF; COMMUNICATION; STRATEGY; PROMOTE; MODEL;
D O I
10.1021/acs.analchem.7b02593
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Interaction between tumor and endothelial cells could affect tumor growth and progression and induce drug resistance during cancer therapy. Investigation of tumor-endothelial cell interaction involves cell coculture, protein detection, and analysis of drug metabolites, which are complicated and time-consuming. In this work, we present an integrated microfluidic device with three individual components (cell coculture component, protein detection component, and pretreatment component for drug metabolites) to probe the interaction between tumor and endothelial cells. Cocultured cervical carcinoma cells (CaSki cells) and human umbilical vein endothelial cells (HUVECs) show higher resistance to chemotherapeutic agents than single-cultured cells, indicated by higher cell viability, increased expression of angiogenic proteins, and elevated level of paclitaxel metabolites under coculture conditions. This integrated microfluidic platform with multiple functions facilitates understanding of the interaction between tumor and endothelial cells, and it may become a promising tool for drug screening, within an engineered tumor microenvironment.
引用
收藏
页码:10037 / 10044
页数:8
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