Carcinoma-associated fibroblasts promoted tumor spheroid invasion on a microfluidic 3D co-culture device

被引:137
作者
Liu, Tingjiao [1 ,2 ]
Lin, Bingcheng [1 ]
Qin, Jianhua [1 ]
机构
[1] Chinese Acad Sci, Dept Biotechnol, Dalian Inst Chem Phys, Beijing 100864, Peoples R China
[2] Dalian Med Univ, Sect Oral Pathol, Coll Stomatol, Dalian, Peoples R China
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
CANCER-CELLS; STROMAL FIBROBLASTS; HOMOTYPIC AGGREGATION; IN-VIVO; MYOFIBROBLASTS; ANGIOGENESIS; EXPRESSION; CULTURE; PROGRESSION; MATRIX;
D O I
10.1039/c000022a
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Carcinoma-associated fibroblasts (CAFs) are a key determinant in malignant progression of cancer and represent an important target for cancer therapies. In this work, we present a microfluidic-based 3D co-culture device to reconstruct an in vitro tumor microenvironment and firstly investigate the effect of CAFs on cancer cell invasion in 3D matrix. This device is composed of six co-culture units, which enable parallel co-culture assays to be run in the presence of 3D extracellular matrix. Salivary gland adenoid cystic carcinoma (ACC) cells and CAFs embedded in matrix were co-cultured without direct contact on the device. Communication between ACC cells and CAFs could be established via medium diffused in matrix. It was observed that CAFs promoted ACC cell invasion in 3D matrix in a spheroid fashion, indicating that CAFs play a critical role in cancer invasion. We further demonstrated the effect of MMP inhibitor as an agent against CAF-promoted cancer invasion. This co-culture device reproducibly reflected the in vivo growth and invasion pattern of ACC and recreated the stroma-regulated ACC invasion. Thus, it provides a suitable platform for elucidating the mechanism of CAF-regulated cancer invasion and discovering anti-invasion drugs in a well defined 3D environment.
引用
收藏
页码:1671 / 1677
页数:7
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