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Simulating the Tumor Microenvironment for Immune Cell Interactions via Deployable Extrusion Bioprinting

Corrado Mazzaglia, View ORCID ProfileYaqi Sheng, Leonor Nunes Rodrigues, View ORCID ProfileIek Man Lei, View ORCID ProfileJacqueline D. Shields, View ORCID ProfileYan Yan Shery Huang
doi: https://doi.org/10.1101/2022.04.08.487692
Corrado Mazzaglia
1MRC Cancer Unit, University of Cambridge, Cambridge, UK
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Yaqi Sheng
2The Nanoscience Centre, University of Cambridge, Cambridge, UK
3Department of Engineering, University of Cambridge, Cambridge, UK
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Leonor Nunes Rodrigues
1MRC Cancer Unit, University of Cambridge, Cambridge, UK
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Iek Man Lei
3Department of Engineering, University of Cambridge, Cambridge, UK
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Jacqueline D. Shields
1MRC Cancer Unit, University of Cambridge, Cambridge, UK
4Comprehensive Cancer Centre, King’s College London, Great Maze pond, London, UK
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  • For correspondence: Jacqueline.Shields@kcl.ac.uk yysh2@cam.ac.uk
Yan Yan Shery Huang
2The Nanoscience Centre, University of Cambridge, Cambridge, UK
3Department of Engineering, University of Cambridge, Cambridge, UK
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  • For correspondence: Jacqueline.Shields@kcl.ac.uk yysh2@cam.ac.uk
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Abstract

Three-dimensional (3D) bioprinting has emerged as a promising tool for constructing tumor microenvironments (TME) for cancer modelling in vitro. Realizing the translational impacts of 3D bioprinting for cancer research necessitates innovation in bioprinting workflows which integrate affordability, user-friendliness, and biological relevance. Herein, we demonstrate ‘bioArm’, a simple, yet highly effective extrusion bioprinting platform, which can be folded into a carry-on pack, and rapidly deployed between bio-facilities. BioArm enabled TME reconstruction in the form of 3D core-shell tumoroids with cancer-associated fibroblasts (CAFs). Tumoroids showed the presence of a heterogenous population of CAFs with de novo synthesized extracellular matrices, demonstrating more in vivo-like characteristics compared to conventional 2D co-culture models. Embedding the 3D printed tumoroids in an immune cell laden collagen matrix permitted tracking of the interaction between immune cells and tumoroids, and subsequent immunotherapy treatments. Our deployable extrusion bioprinting workflow could significantly widen the accessibility of 3D bioprinting for gaining mechanistic understanding in TME, and for developing strategies in cancer drug testing.

Competing Interest Statement

The authors have declared no competing interest.

Copyright 
The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. All rights reserved. No reuse allowed without permission.
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Posted April 10, 2022.
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Simulating the Tumor Microenvironment for Immune Cell Interactions via Deployable Extrusion Bioprinting
Corrado Mazzaglia, Yaqi Sheng, Leonor Nunes Rodrigues, Iek Man Lei, Jacqueline D. Shields, Yan Yan Shery Huang
bioRxiv 2022.04.08.487692; doi: https://doi.org/10.1101/2022.04.08.487692
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Simulating the Tumor Microenvironment for Immune Cell Interactions via Deployable Extrusion Bioprinting
Corrado Mazzaglia, Yaqi Sheng, Leonor Nunes Rodrigues, Iek Man Lei, Jacqueline D. Shields, Yan Yan Shery Huang
bioRxiv 2022.04.08.487692; doi: https://doi.org/10.1101/2022.04.08.487692

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