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Examining metastatic behavior within 3D bioprinted vasculature for the validation of a 3D computational flow model

Understanding the dynamics of circulating tumor cell (CTC) behavior within the vasculature has remained an elusive goal in cancer biology. To elucidate the contribution of hydrodynamics in determining sites of CTC vascular colonization, the physical forces affecting these cells must be evaluated in...

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Autores principales: Hynes, W. F., Pepona, M., Robertson, C., Alvarado, J., Dubbin, K., Triplett, M., Adorno, J. J., Randles, A., Moya, M. L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Association for the Advancement of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7449690/
https://www.ncbi.nlm.nih.gov/pubmed/32923637
http://dx.doi.org/10.1126/sciadv.abb3308
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author Hynes, W. F.
Pepona, M.
Robertson, C.
Alvarado, J.
Dubbin, K.
Triplett, M.
Adorno, J. J.
Randles, A.
Moya, M. L.
author_facet Hynes, W. F.
Pepona, M.
Robertson, C.
Alvarado, J.
Dubbin, K.
Triplett, M.
Adorno, J. J.
Randles, A.
Moya, M. L.
author_sort Hynes, W. F.
collection PubMed
description Understanding the dynamics of circulating tumor cell (CTC) behavior within the vasculature has remained an elusive goal in cancer biology. To elucidate the contribution of hydrodynamics in determining sites of CTC vascular colonization, the physical forces affecting these cells must be evaluated in a highly controlled manner. To this end, we have bioprinted endothelialized vascular beds and perfused these constructs with metastatic mammary gland cells under physiological flow rates. By pairing these in vitro devices with an advanced computational flow model, we found that the bioprinted analog was readily capable of evaluating the accuracy and integrated complexity of a computational flow model, while also highlighting the discrete contribution of hydrodynamics in vascular colonization. This intersection of these two technologies, bioprinting and computational simulation, is a key demonstration in the establishment of an experimentation pipeline for the understanding of complex biophysical events.
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spelling pubmed-74496902020-09-11 Examining metastatic behavior within 3D bioprinted vasculature for the validation of a 3D computational flow model Hynes, W. F. Pepona, M. Robertson, C. Alvarado, J. Dubbin, K. Triplett, M. Adorno, J. J. Randles, A. Moya, M. L. Sci Adv Research Articles Understanding the dynamics of circulating tumor cell (CTC) behavior within the vasculature has remained an elusive goal in cancer biology. To elucidate the contribution of hydrodynamics in determining sites of CTC vascular colonization, the physical forces affecting these cells must be evaluated in a highly controlled manner. To this end, we have bioprinted endothelialized vascular beds and perfused these constructs with metastatic mammary gland cells under physiological flow rates. By pairing these in vitro devices with an advanced computational flow model, we found that the bioprinted analog was readily capable of evaluating the accuracy and integrated complexity of a computational flow model, while also highlighting the discrete contribution of hydrodynamics in vascular colonization. This intersection of these two technologies, bioprinting and computational simulation, is a key demonstration in the establishment of an experimentation pipeline for the understanding of complex biophysical events. American Association for the Advancement of Science 2020-08-26 /pmc/articles/PMC7449690/ /pubmed/32923637 http://dx.doi.org/10.1126/sciadv.abb3308 Text en Copyright © 2020 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/ https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited.
spellingShingle Research Articles
Hynes, W. F.
Pepona, M.
Robertson, C.
Alvarado, J.
Dubbin, K.
Triplett, M.
Adorno, J. J.
Randles, A.
Moya, M. L.
Examining metastatic behavior within 3D bioprinted vasculature for the validation of a 3D computational flow model
title Examining metastatic behavior within 3D bioprinted vasculature for the validation of a 3D computational flow model
title_full Examining metastatic behavior within 3D bioprinted vasculature for the validation of a 3D computational flow model
title_fullStr Examining metastatic behavior within 3D bioprinted vasculature for the validation of a 3D computational flow model
title_full_unstemmed Examining metastatic behavior within 3D bioprinted vasculature for the validation of a 3D computational flow model
title_short Examining metastatic behavior within 3D bioprinted vasculature for the validation of a 3D computational flow model
title_sort examining metastatic behavior within 3d bioprinted vasculature for the validation of a 3d computational flow model
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7449690/
https://www.ncbi.nlm.nih.gov/pubmed/32923637
http://dx.doi.org/10.1126/sciadv.abb3308
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