Adaptable stirred-tank culture strategies for large scale production of multicellular spheroid-based tumor cell models

被引:92
作者
Santo, Vitor E. [1 ,2 ]
Estrada, Marta F. [1 ,2 ]
Rebelo, Sofia P. [1 ,2 ]
Abreu, Sofia [1 ,2 ]
Silva, Ines [1 ,2 ]
Pinto, Catarina [1 ,2 ]
Veloso, Susana C. [1 ,2 ]
Serra, Ana Teresa [1 ,2 ]
Boghaert, Erwin [3 ]
Alves, Paula M. [1 ,2 ]
Brito, Catarina [1 ,2 ]
机构
[1] Inst Biol Expt Tecnol, iBET, Apartado 12, P-2780901 Oeiras, Portugal
[2] Univ Nova Lisboa, Inst Tecnol Quim & Biol Antonio Xavier, Ave Republ, P-2780157 Oeiras, Portugal
[3] AbbVie Inc, N Chicago, IL 60064 USA
关键词
In vitro cancer models; Tumor spheroids; Stirred-tank culture systems; Drug discovery; 3D cell culture; PLURIPOTENT STEM-CELLS; 3-DIMENSIONAL CULTURE; CANCER CELLS; GROWTH; DIFFERENTIATION; CARCINOMA; MICROENVIRONMENT; MORPHOGENESIS; GENERATION; EXPRESSION;
D O I
10.1016/j.jbiotec.2016.01.031
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Currently there is an effort toward the development of in vitro cancer models more predictive of clinical efficacy. The onset of advanced analytical tools and imaging technologies has increased the utilization of spheroids in the implementation of high throughput approaches in drug discovery. Agitation-based culture systems are commonly proposed as an alternative method for the production of tumor spheroids, despite the scarce experimental evidence found in the literature. In this study, we demonstrate the robustness and reliability of stirred-tank cultures for the scalable generation of 3D cancer models. We developed standardized protocols to a panel of tumor cell lines from different pathologies and attained efficient tumor cell aggregation by tuning hydrodynamic parameters. Large numbers of spheroids were obtained (typically 1000-1500 spheroids/mL) presenting features of native tumors, namely morphology, proliferation and hypoxia gradients, in a cell line-dependent mode. Heterotypic 3D cancer models, based on co-cultures of tumor cells and fibroblasts, were also established in the absence or presence of additional physical support from an alginate matrix, with maintenance of high cell viability. Altogether, we demonstrate that 3D tumor cell model production in stirred-tank culture systems is a robust and versatile approach, providing reproducible tools for drug screening and target verification in pre-clinical oncology research. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:118 / 129
页数:12
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