Microfluidic modelling of the tumor microenvironment for anti-cancer drug development

被引:174
|
作者
Shang, Menglin [1 ,3 ]
Soon, Ren Hao [3 ]
Lim, Chwee Teck [1 ,2 ,3 ,4 ,5 ]
Khoo, Bee Luan [1 ]
Han, Jongyoon [1 ,6 ]
机构
[1] Singapore MIT Alliance Res & Technol SMART Ctr, BioSyst & Micromech BioSyM IRG, 1 Create Way,Enterprise Wing, Singapore 138602, Singapore
[2] Natl Univ Singapore, Mechanobiol Inst, Singapore, Singapore
[3] Natl Univ Singapore, Dept Biomed Engn, 7 Engn Dr 1, Singapore 117574, Singapore
[4] Natl Univ Singapore, Dept Mech Engn, Singapore, Singapore
[5] Natl Univ Singapore, Biomed Inst Global Hlth Res & Technol, Singapore, Singapore
[6] MIT, Dept Biol Engn, Dept Elect Engn & Comp Sci, 77 Massachusetts Ave, Cambridge, MA 02139 USA
关键词
INTERSTITIAL FLUID PRESSURE; 3-DIMENSIONAL CELL-CULTURE; ENGINEERED MOUSE MODELS; ON-A-CHIP; BREAST-CANCER; GENE-EXPRESSION; BLOOD-VESSELS; EXTRACELLULAR-MATRIX; ENDOTHELIAL BARRIER; SPHEROID CULTURE;
D O I
10.1039/c8lc00970h
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Cancer is the leading cause of death worldwide. The complex and disorganized tumor microenvironment makes it very difficult to treat this disease. The most common in vitro drug screening method now is based on 2D culture models which poorly represent actual tumors. Therefore, many 3D tumor models which are more physiologically relevant have been developed to conduct in vitro drug screening and alleviate this situation. Among all these models, the microfluidic tumor model has the unique advantage of recapitulating the tumor microenvironment in a comparatively easier and representative fashion. While there are many review papers available on the related topic of microfluidic tumor models, in this review we aim to focus more on the possibility of generating clinically actionable information from these microfluidic systems, besides scientific insight. Our topics cover the tumor microenvironment, conventional 2D and 3D cultures, animal models, and microfluidic tumor models, emphasizing their link to anti-cancer drug discovery and personalized medicine.
引用
收藏
页码:369 / 386
页数:18
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