Bourn, M.D., Mohajerani, S., Mavria, G. et al. (4 more authors) (2022) Targeting Tumour Vasculature using Integrin αvβ3 -Observation of Liposome Accumulation in Microfluidic Vasculature Networks. In: 25th International Conference on Proceedings of Miniaturized Systems for Chemistry and Life Sciences (MicroTAS 2021). 25th International Conference on Miniaturized Systems for Chemistry and Life Sciences (MicroTAS 2021), 10-14 Oct 2021, Palm Springs, USA. Chemical and Biological Microsystems Society (CBMS) , pp. 325-326. ISBN 9781713855736
Abstract
This paper reports the use of perfusable microfluidic vasculature networks to investigate the use αvβ3 integrin-targeted liposomes as tumour vasculature targeting agents. Endothelial cells co-cultured with fibroblasts were induced to self-assemble into vasculature networks using pro-angiogenic growth factors. Tumour vasculature was mimicked by growing networks in tumour-cell conditioned media (TCM), taken from HCT116 cell cultures. Assessment of αvβ3 expression using immunostaining and flow cytometry observed the upregulation of αvβ3 expression on endothelial cells grown in TCM. Results observed increased liposome accumulation in tumour conditioned networks, suggesting αvβ3 may be a promising target for anti-cancer therapeutics.
Metadata
Item Type: | Proceedings Paper |
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Authors/Creators: |
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Dates: |
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Institution: | The University of Leeds |
Academic Units: | The University of Leeds > Faculty of Medicine and Health (Leeds) > School of Medicine (Leeds) > Leeds Institute of Medical Research (LIMR) > Division of Molecular Medicine The University of Leeds > Faculty of Engineering & Physical Sciences (Leeds) > School of Physics and Astronomy (Leeds) > Molecular & Nanoscale Physics |
Funding Information: | Funder Grant number EPSRC (Engineering and Physical Sciences Research Council) EP/P023266/1 |
Depositing User: | Symplectic Publications |
Date Deposited: | 25 Mar 2024 11:04 |
Last Modified: | 25 Mar 2024 11:04 |
Published Version: | https://www.proceedings.com/64786.html |
Status: | Published |
Publisher: | Chemical and Biological Microsystems Society (CBMS) |
Open Archives Initiative ID (OAI ID): | oai:eprints.whiterose.ac.uk:210799 |