Issue 20, 2022

A high-throughput 3D bioprinted cancer cell migration and invasion model with versatile and broad biological applicability

Abstract

Understanding the underlying mechanisms of migration and metastasis is a key focus of cancer research. There is an urgent need to develop in vitro 3D tumor models that can mimic physiological cell–cell and cell–extracellular matrix interactions, with high reproducibility and that are suitable for high throughput (HTP) drug screening. Here, we developed a HTP 3D bioprinted migration model using a bespoke drop-on-demand bioprinting platform. This HTP platform coupled with tunable hydrogel systems enables (i) the rapid encapsulation of cancer cells within in vivo tumor mimicking matrices, (ii) in situ and real-time measurement of cell movement, (iii) detailed molecular analysis for the study of mechanisms underlying cell migration and invasion, and (iv) the identification of novel therapeutic options. This work demonstrates that this HTP 3D bioprinted cell migration platform has broad applications across quantitative cell and cancer biology as well as drug screening.

Graphical abstract: A high-throughput 3D bioprinted cancer cell migration and invasion model with versatile and broad biological applicability

Supplementary files

Article information

Article type
Paper
Submitted
07 اردیبهشت 1401
Accepted
29 تیر 1401
First published
01 مهر 1401
This article is Open Access
Creative Commons BY-NC license

Biomater. Sci., 2022,10, 5876-5887

A high-throughput 3D bioprinted cancer cell migration and invasion model with versatile and broad biological applicability

M. Jung, J. N. Skhinas, E. Y. Du, M. A. K. Tolentino, R. H. Utama, M. Engel, A. Volkerling, A. Sexton, A. P. O'Mahony, J. C. C. Ribeiro, J. J. Gooding and M. Kavallaris, Biomater. Sci., 2022, 10, 5876 DOI: 10.1039/D2BM00651K

This article is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported Licence. You can use material from this article in other publications, without requesting further permission from the RSC, provided that the correct acknowledgement is given and it is not used for commercial purposes.

To request permission to reproduce material from this article in a commercial publication, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party commercial publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements