新生血管
血管内皮生长因子
绒毛尿囊膜
内皮干细胞
肿瘤微环境
血管生成抑制剂
体内
脐静脉
癌细胞
治疗性血管生成
细胞生物学
基质凝胶
癌症
转移
血管内皮生长因子A
医学
作者
Lilu Liu,Zhaorong Xie,Wenyuan Zhang,Shimeng Fang,Jing Kong,Dong Jin,Jiao Li,Xiaojie Li,Xuesong Yang,Yong Luo,Bingcheng Lin,Tingjiao Liu
出处
期刊:RSC Advances
[Royal Society of Chemistry]
日期:2016-04-11
卷期号:6 (42): 35248-35256
被引量:14
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, time-saving, and rapid alternative to animal models.
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