Towards automated production and drug sensitivity testing using scaffold-free spherical tumor microtissues

被引:100
作者
Drewitz, Maren [1 ]
Helbling, Marianne [1 ]
Fried, Nicole [1 ]
Bieri, Manuela [1 ]
Moritz, Wolfgang [1 ]
Lichtenberg, Jan [1 ]
Kelm, Jens M. [1 ]
机构
[1] InSphero AG, CH-8005 Zurich, Switzerland
关键词
Cell-based assays; Drug discovery; Drug screening; High throughput; Tissue engineering; 3-DIMENSIONAL CULTURE; CELL-CULTURE; IN-VIVO; DIFFERENTIATION; SPHEROIDS; HYDROGELS; EFFICACY; THERAPY; HYPOXIA; DESIGN;
D O I
10.1002/biot.201100290
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Although the relevance of three-dimensional (3-D) culture has been recognized for years and exploited at an academic level, its translation to industrial applications has been slow. The development of reliable high-throughput technologies is clearly a prerequisite for the industrial implementation of 3-D models. In this study the robustness of spherical microtissue production and drug testing in a 96-well hanging-drop multiwell plate format was assessed on a standard 96-well channel robotic platform. Microtissue models derived from six different cell lines were produced and characterized according to their growth profile and morphology displaying high-density tissue-like reformation and growth over at least 15 days. The colon cancer cell line HCT116 was chosen as a model to assess microtissue-based assay reproducibility. Within three individual production batches the size variations of the produced microtissues were below 5%. Reliability of the microtissue-based assay was tested using two reference compounds, staurosporine and chlorambucil. In four independent drug testings the calculated IC50 values were benchmarked against 2-D multiwell testings displaying similar consistency. The technology presented here for the automated production of a variety of microtissues for efficacy testing in a standard 96-well format will aid the implementation of more organotypic models at an early time point in the drug discovery process.
引用
收藏
页码:1488 / 1496
页数:9
相关论文
共 38 条
[1]   Cell culture: Biology's new dimension [J].
Abbott, A .
NATURE, 2003, 424 (6951) :870-872
[2]   Putting tumours in context [J].
Bissell, MJ ;
Radisky, D .
NATURE REVIEWS CANCER, 2001, 1 (01) :46-54
[3]  
Comley J., 2010, 3D CELL CULTURE EASI, P25
[4]   Contribution of three-dimensional culture to cancer research [J].
Desoize, B .
CRITICAL REVIEWS IN ONCOLOGY HEMATOLOGY, 2000, 36 (2-3) :59-60
[5]   Hydrogels for tissue engineering: scaffold design variables and applications [J].
Drury, JL ;
Mooney, DJ .
BIOMATERIALS, 2003, 24 (24) :4337-4351
[6]   Cell-interactive 3D-scaffold; advances and applications [J].
Dutta, Ranjna C. ;
Dutta, Aroop K. .
BIOTECHNOLOGY ADVANCES, 2009, 27 (04) :334-339
[7]   Experimental anti-tumor therapy in 3-D: Spheroids - old hat or new challenge? [J].
Friedrich, Juergen ;
Ebner, Reinhard ;
Kunz-Schughart, Leoni A. .
INTERNATIONAL JOURNAL OF RADIATION BIOLOGY, 2007, 83 (11-12) :849-871
[8]   Tumor pH controls the in vivo efficacy of weak acid and base chemotherapeutics [J].
Gerweck, LE ;
Vijayappa, S ;
Kozin, S .
MOLECULAR CANCER THERAPEUTICS, 2006, 5 (05) :1275-1279
[9]   Comparative efficacy of novel platinum(IV) compounds with established chemotherapeutic drugs in solid tumour models [J].
Hall, MD ;
Martin, C ;
Ferguson, DJP ;
Phillips, RM ;
Hambley, TW ;
Callaghan, R .
BIOCHEMICAL PHARMACOLOGY, 2004, 67 (01) :17-30
[10]   Multicellular spheroids as an in vitro tumor model [J].
Hamilton, G .
CANCER LETTERS, 1998, 131 (01) :29-34