Drug Discovery Approaches Utilizing Three-Dimensional Cell Culture

被引:71
作者
Ryan, Sarah-Louise [1 ,2 ]
Baird, Anne-Marie [1 ,2 ,3 ]
Vaz, Gisela [4 ]
Urquhart, Aaron J. [1 ,2 ]
Senge, Mathias [4 ]
Richard, Derek J. [1 ]
O'Byrne, Kenneth J. [1 ,3 ,5 ]
Davies, Anthony M. [2 ,6 ]
机构
[1] Queensland Univ Technol, Canc & Ageing Res Program, Inst Hlth & Biomed Innovat, Brisbane, Qld 4001, Australia
[2] Queensland Univ Technol, Translat Cell Imaging Queensland, Inst Hlth & Biomed Innovat, TRI Level 3,37 Kent St, Brisbane, Qld 4102, Australia
[3] Univ Dublin Trinity Coll, Inst Mol Med, Thorac Oncol Res Grp, Dublin 2, Ireland
[4] Univ Dublin Trinity Coll, Med Chem Res Grp, Inst Mol Med, Dublin 2, Ireland
[5] Princess Alexandra Hosp, Div Canc Serv, Brisbane, Qld 4102, Australia
[6] Univ Dublin Trinity Coll, Irish Natl Ctr High Content Screening & Anal, Inst Mol Med, Dublin 2, Ireland
关键词
EXTRACELLULAR-MATRIX; IN-VITRO; MULTICELLULAR SPHEROIDS; TISSUE ARCHITECTURE; LIVER-CELLS; CANCER; MODELS; SCAFFOLDS; 3-D; MICROENVIRONMENTS;
D O I
10.1089/adt.2015.670
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Historically, two-dimensional (2D) cell culture has been the preferred method of producing disease models in vitro. Recently, there has been a move away from 2D culture in favor of generating three-dimensional (3D) multicellular structures, which are thought to be more representative of the in vivo environment. This transition has brought with it an influx of technologies capable of producing these structures in various ways. However, it is becoming evident that many of these technologies do not perform well in automated in vitro drug discovery units. We believe that this is a result of their incompatibility with high-throughput screening (HTS). In this study, we review a number of technologies, which are currently available for producing in vitro 3D disease models. We assess their amenability with high-content screening and HTS and highlight our own work in attempting to address many of the practical problems that are hampering the successful deployment of 3D cell systems in mainstream research.
引用
收藏
页码:19 / 28
页数:10
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