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Microarrays for the scalable production of metabolically relevant tumour spheroids: a tool for modulating chemosensitivity traits

Microarrays for the scalable production of metabolically relevant tumour spheroids: a tool for modulating chemosensitivity traits
Microarrays for the scalable production of metabolically relevant tumour spheroids: a tool for modulating chemosensitivity traits
We report the use of thin film poly(dimethylsiloxane) (PDMS) prints for the arrayed mass production of highly uniform 3-D human HT29 colon carcinoma spheroids. The spheroids have an organotypic density and, as determined by 3-axis imaging, were genuinely spherical. Critically, the array density impacts growth kinetics and can be tuned to produce spheroids ranging in diameter from 200 to 550 mu m. The diffusive limit of competition for media occurred with a pitch of >= 1250 mu m and was used for the optimal array-based culture of large, viable spheroids. During sustained culture mass transfer gradients surrounding and within the spheroids are established, and lead to growth cessation, altered expression patterns and the formation of a central secondary necrosis. These features reflect the microenvironment of avascularised tumours, making the array format well suited for the production of model tumours with defined sizes and thus defined spatio-temporal pathophysiological gradients. Experimental windows, before and after the onset of hypoxia, were identified and used with an enzyme activity-based viability assay to measure the chemosensitivity towards irinotecan. Compared to monolayer cultures, a marked reduction in the drug efficacy towards the different spheroid culture states was observed and attributed to cell cycle arrest, the 3-D character, scale and/or hypoxia factors. In summary, spheroid culture using the array format has great potential to support drug discovery and development, as well as tumour biology research.
acid-phosphatase assay, culture-system, hepatocyte spheroids, topoisomerase-i, cell viability, growth, microfabrication, differentiation, camptothecin generation
1473-0197
419-428
Hardelauf, Heike
ff18e0f8-62ed-4edf-9746-f72701657440
Frimat, Jean-Philippe
a15e6f17-c613-449d-88ca-18bb92f0834f
Stewart, Joanna D.
e1ec9784-39cc-48ed-9f4f-2a05d25f2106
Schormann, Wiebke
b14d2d98-98c8-4ed3-885f-bc30d8b4d167
Chiang, Ya-Yu
0ab4fe9e-9a3e-4594-a13c-73f68c13b8b3
Lampen, Peter
4dad0c26-3adf-4076-b950-e00fe58e5db4
Franzke, Joachim
711b7072-1f6c-44e7-b33c-66a9c8304f77
Hengstler, Jan G.
8b1695f3-3506-400f-85ae-44b875949445
Cadenas, Cristina
28c017c5-5bb8-4845-8d18-2867dc3a78aa
Kunz-Schughart, Leoni A.
7245c975-fa00-4e20-939a-60aba8c93d15
West, Jonathan
f1c2e060-16c3-44c0-af70-242a1c58b968
Hardelauf, Heike
ff18e0f8-62ed-4edf-9746-f72701657440
Frimat, Jean-Philippe
a15e6f17-c613-449d-88ca-18bb92f0834f
Stewart, Joanna D.
e1ec9784-39cc-48ed-9f4f-2a05d25f2106
Schormann, Wiebke
b14d2d98-98c8-4ed3-885f-bc30d8b4d167
Chiang, Ya-Yu
0ab4fe9e-9a3e-4594-a13c-73f68c13b8b3
Lampen, Peter
4dad0c26-3adf-4076-b950-e00fe58e5db4
Franzke, Joachim
711b7072-1f6c-44e7-b33c-66a9c8304f77
Hengstler, Jan G.
8b1695f3-3506-400f-85ae-44b875949445
Cadenas, Cristina
28c017c5-5bb8-4845-8d18-2867dc3a78aa
Kunz-Schughart, Leoni A.
7245c975-fa00-4e20-939a-60aba8c93d15
West, Jonathan
f1c2e060-16c3-44c0-af70-242a1c58b968

Hardelauf, Heike, Frimat, Jean-Philippe, Stewart, Joanna D., Schormann, Wiebke, Chiang, Ya-Yu, Lampen, Peter, Franzke, Joachim, Hengstler, Jan G., Cadenas, Cristina, Kunz-Schughart, Leoni A. and West, Jonathan (2011) Microarrays for the scalable production of metabolically relevant tumour spheroids: a tool for modulating chemosensitivity traits. Lab on a Chip, 11 (3), 419-428. (doi:10.1039/C0LC00089B). (PMID:21079873)

Record type: Article

Abstract

We report the use of thin film poly(dimethylsiloxane) (PDMS) prints for the arrayed mass production of highly uniform 3-D human HT29 colon carcinoma spheroids. The spheroids have an organotypic density and, as determined by 3-axis imaging, were genuinely spherical. Critically, the array density impacts growth kinetics and can be tuned to produce spheroids ranging in diameter from 200 to 550 mu m. The diffusive limit of competition for media occurred with a pitch of >= 1250 mu m and was used for the optimal array-based culture of large, viable spheroids. During sustained culture mass transfer gradients surrounding and within the spheroids are established, and lead to growth cessation, altered expression patterns and the formation of a central secondary necrosis. These features reflect the microenvironment of avascularised tumours, making the array format well suited for the production of model tumours with defined sizes and thus defined spatio-temporal pathophysiological gradients. Experimental windows, before and after the onset of hypoxia, were identified and used with an enzyme activity-based viability assay to measure the chemosensitivity towards irinotecan. Compared to monolayer cultures, a marked reduction in the drug efficacy towards the different spheroid culture states was observed and attributed to cell cycle arrest, the 3-D character, scale and/or hypoxia factors. In summary, spheroid culture using the array format has great potential to support drug discovery and development, as well as tumour biology research.

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More information

e-pub ahead of print date: 16 November 2010
Published date: 2011
Keywords: acid-phosphatase assay, culture-system, hepatocyte spheroids, topoisomerase-i, cell viability, growth, microfabrication, differentiation, camptothecin generation
Organisations: Cancer Sciences

Identifiers

Local EPrints ID: 346447
URI: http://eprints.soton.ac.uk/id/eprint/346447
ISSN: 1473-0197
PURE UUID: 3bf31136-d634-424f-bbfe-ae748a58e914
ORCID for Joanna D. Stewart: ORCID iD orcid.org/0000-0002-2608-1967
ORCID for Jonathan West: ORCID iD orcid.org/0000-0002-5709-6790

Catalogue record

Date deposited: 15 Jan 2013 13:56
Last modified: 15 Mar 2024 03:43

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Contributors

Author: Heike Hardelauf
Author: Jean-Philippe Frimat
Author: Joanna D. Stewart ORCID iD
Author: Wiebke Schormann
Author: Ya-Yu Chiang
Author: Peter Lampen
Author: Joachim Franzke
Author: Jan G. Hengstler
Author: Cristina Cadenas
Author: Leoni A. Kunz-Schughart
Author: Jonathan West ORCID iD

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