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A rapid high throughput bioprinted colorectal cancer spheroid platform forin vitrodrug- and radiation-response.
Johnson, Peter A; Menegatti, Sara; Chambers, Adam C; Alibhai, Dominic; Collard, Tracey J; Williams, Ann C; Bayley, Hagan; Perriman, Adam W.
Afiliação
  • Johnson PA; Department of Chemistry, University of Oxford, Oxford OX1 3TA, United Kingdom.
  • Menegatti S; School of Cellular and Molecular Medicine, University of Bristol, Bristol BS8 1TD, United Kingdom.
  • Chambers AC; School of Cellular and Molecular Medicine, University of Bristol, Bristol BS8 1TD, United Kingdom.
  • Alibhai D; Wolfson Bioimaging Facility, University of Bristol, Bristol BS8 1TD, United Kingdom.
  • Collard TJ; School of Cellular and Molecular Medicine, University of Bristol, Bristol BS8 1TD, United Kingdom.
  • Williams AC; School of Cellular and Molecular Medicine, University of Bristol, Bristol BS8 1TD, United Kingdom.
  • Bayley H; Department of Chemistry, University of Oxford, Oxford OX1 3TA, United Kingdom.
  • Perriman AW; School of Cellular and Molecular Medicine, University of Bristol, Bristol BS8 1TD, United Kingdom.
Biofabrication ; 15(1)2022 Nov 02.
Article em En | MEDLINE | ID: mdl-36321254
ABSTRACT
We describe the development of a high-throughput bioprinted colorectal cancer (CRC) spheroid platform with high levels of automation, information content, and low cell number requirement. This is achieved via the formulation of a hydrogel bioink with a compressive Young's modulus that is commensurate with that of colonic tissue (1-3 kPa), which supports exponential growth of spheroids from a wide range of CRC cell lines. The resulting spheroids display tight cell-cell junctions, bioink matrix-cell interactions and necrotic hypoxic cores. By combining high content light microscopy imaging and processing with rapid multiwell plate bioprinting, dose-response profiles are generated from CRC spheroids challenged with oxaliplatin (OX) and fluorouracil (5FU), as well as radiotherapy. Bioprinted CRC spheroids are shown to exhibit high levels of chemoresistance relative to cell monolayers, and OX was found to be significantly less effective against tumour spheroids than in monolayer culture, when compared to 5FU.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Colorretais / Bioimpressão Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Colorretais / Bioimpressão Idioma: En Ano de publicação: 2022 Tipo de documento: Article