Biomimetic tumor-induced angiogenesis and anti-angiogenic therapy in a microfluidic model

被引:25
|
作者
Liu, Lilu [1 ]
Xie, Zhaorong [1 ]
Zhang, Wenyuan [1 ]
Fang, Shimeng [1 ]
Kong, Jing [1 ]
Jin, Dong [1 ]
Li, Jiao [1 ]
Li, Xiaojie [1 ]
Yang, Xuesong [2 ]
Luo, Yong [3 ]
Lin, Bingcheng [3 ,4 ]
Liu, Tingjiao [1 ]
机构
[1] Dalian Med Univ, Coll Stomatol, Sect Oral Pathol, West Sect 9,South Rd Lvshun, Dalian 116044, Peoples R China
[2] Dalian Med Univ, Liaoning Prov Core Lab Glycobiol & Glycoengn, Dept Biochem & Mol Biol, Dalian, Peoples R China
[3] Dalian Univ Technol, Fac Chem Environm & Biol Sci & Technol, 2 Linggong Rd, Dalian 116024, Peoples R China
[4] Chinese Acad Sci, Dalian Inst Chem Phys, Dept Biotechnol, 457 Zhongshan Rd, Dalian 116023, Peoples R China
来源
RSC ADVANCES | 2016年 / 6卷 / 42期
基金
中国国家自然科学基金;
关键词
ENDOTHELIAL GROWTH-FACTOR; CELL-INTERACTIONS; IN-VITRO; CANCER; EXPRESSION; MORPHOGENESIS; COCULTURE; PHOSPHORYLATION; ANGIOPOIETIN-2; MICROVESSELS;
D O I
10.1039/c6ra05645h
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We developed a biomimetic microfluidic model to reproduce hallmark events of tumor-induced angiogenesis. The angiogenic capabilities of salivary gland adenoid cystic carcinoma (ACC) cells and oral squamous cell carcinoma (SCC) cells were assessed in this model. The traditional nude mouse xenograft model was used to investigate the physiological similarity of the microfluidic model to animal models, and the results showed that the angiogenic potential of ACC and SCC cells assessed by the microfluidic model was in agreement with the results obtained from the nude mouse model. The microfluidic model was subsequently used to evaluate the effect of antiangiogenic drugs on ACC- and SCC-induced angiogenesis. The antiangiogenic effect of anti-VEGF was further compared between the microfluidic and nude mouse models, and showed that it effectively inhibited tumor-induced angiogenesis in both the microfluidic model and the nude mouse model. Thus, tumor-induced angiogenesis reproduced in the microfluidic model may expand the capabilities of cell culture models, providing a low-cost, timesaving, and rapid alternative to animal models.
引用
收藏
页码:35248 / 35256
页数:9
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