Engineering cancer microenvironments for in vitro 3-D tumor models

被引:254
作者
Asghar, Waseem [1 ,2 ]
El Assal, Rami [1 ]
Shafiee, Hadi [3 ]
Pitteri, Sharon [4 ]
Paulmurugan, Ramasamy [4 ]
Demirci, Utkan [1 ,3 ,4 ]
机构
[1] Stanford Univ, Demirci Bioacoust MEMS Med BAMM Labs, Canary Ctr Stanford Canc Early Detect, Dept Radiol,Stanford Sch Med, Palo Alto, CA 94304 USA
[2] Florida Atlantic Univ, Dept Comp Engn & Elect Engn & Comp Sci, Boca Raton, FL 33431 USA
[3] Harvard Univ, Demirci Bioacoust MEMS Med BAMM Labs, Brigham & Womens Hosp,Med Sch, Div Biomed Engn,Div Infect Dis,Renal Div,Dept Med, Cambridge, MA 02139 USA
[4] Stanford Univ, Dept Radiol, Canary Ctr Stanford Canc Early Detect, Stanford Sch Med, Palo Alto, CA 94304 USA
基金
美国国家科学基金会;
关键词
ASSEMBLING PEPTIDE HYDROGEL; BASEMENT-MEMBRANE; CELL-CULTURE; 3D CULTURE; MULTICELLULAR ORGANIZATION; SPHEROID CULTURE; EPITHELIAL-CELLS; PROSTATE-CANCER; EMBRYOID BODIES; IMMUNE-SYSTEM;
D O I
10.1016/j.mattod.2015.05.002
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
The natural microenvironment of tumors is composed of extracellular matrix (ECM), blood vasculature, and supporting stromal cells. The physical characteristics of ECM as well as the cellular components play a vital role in controlling cancer cell proliferation, apoptosis, metabolism, and differentiation. To mimic the tumor microenvironment outside the human body for drug testing, two-dimensional (2-D) and murine tumor models are routinely used. Although these conventional approaches are employed in preclinical studies, they still present challenges. For example, murine tumor models are expensive and difficult to adopt for routine drug screening. On the other hand, 2-D in vitro models are simple to perform, but they do not recapitulate natural tumor microenvironment, because they do not capture important three-dimensional (3-D) cell-cell, cell-matrix signaling pathways, and multi-cellular heterogeneous components of the tumor microenvironment such as stromal and immune cells. The three-dimensional (3-D) in vitro tumor models aim to closely mimic cancer microenvironments and have emerged as an alternative to routinely used methods for drug screening. Herein, we review recent advances in 3-D tumor model generation and highlight directions for future applications in drug testing.
引用
收藏
页码:539 / 553
页数:15
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