Microfluidic vascular models of tumor cell extravasation

<jats:p>Emerging microfluidic disease models have amply demonstrated their value in many fields of cancer research. These <jats:italic>in vitro</jats:italic> technologies recapitulate key aspects of metastatic cancer, including the process of tumor cell arrest and extravasation at...

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Main Authors: Kim, Seunggyu, Wan, Zhengpeng, Jeon, Jessie S., Kamm, Roger D.
Other Authors: Massachusetts Institute of Technology. Mechanobiology Laboratory
Format: Article
Published: Frontiers Media SA 2022
Subjects:
Online Access:https://hdl.handle.net/1721.1/146568
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author Kim, Seunggyu
Wan, Zhengpeng
Jeon, Jessie S.
Kamm, Roger D.
author2 Massachusetts Institute of Technology. Mechanobiology Laboratory
author_facet Massachusetts Institute of Technology. Mechanobiology Laboratory
Kim, Seunggyu
Wan, Zhengpeng
Jeon, Jessie S.
Kamm, Roger D.
author_sort Kim, Seunggyu
collection MIT
description <jats:p>Emerging microfluidic disease models have amply demonstrated their value in many fields of cancer research. These <jats:italic>in vitro</jats:italic> technologies recapitulate key aspects of metastatic cancer, including the process of tumor cell arrest and extravasation at the site of the metastatic tumor. To date, extensive efforts have been made to capture key features of the microvasculature to reconstitute the pre-metastatic niche and investigate dynamic extravasation behaviors using microfluidic systems. In this mini-review, we highlight recent microfluidic vascular models of tumor cell extravasation and explore how this approach contributes to development of <jats:italic>in vitro</jats:italic> disease models to enhance understanding of metastasis <jats:italic>in vivo</jats:italic>.</jats:p>
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spelling mit-1721.1/1465682023-02-16T16:20:06Z Microfluidic vascular models of tumor cell extravasation Kim, Seunggyu Wan, Zhengpeng Jeon, Jessie S. Kamm, Roger D. Massachusetts Institute of Technology. Mechanobiology Laboratory Massachusetts Institute of Technology. Department of Mechanical Engineering Cancer Research Oncology <jats:p>Emerging microfluidic disease models have amply demonstrated their value in many fields of cancer research. These <jats:italic>in vitro</jats:italic> technologies recapitulate key aspects of metastatic cancer, including the process of tumor cell arrest and extravasation at the site of the metastatic tumor. To date, extensive efforts have been made to capture key features of the microvasculature to reconstitute the pre-metastatic niche and investigate dynamic extravasation behaviors using microfluidic systems. In this mini-review, we highlight recent microfluidic vascular models of tumor cell extravasation and explore how this approach contributes to development of <jats:italic>in vitro</jats:italic> disease models to enhance understanding of metastasis <jats:italic>in vivo</jats:italic>.</jats:p> 2022-11-21T16:59:14Z 2022-11-21T16:59:14Z 2022-11-11 Article http://purl.org/eprint/type/JournalArticle 2234-943X https://hdl.handle.net/1721.1/146568 Kim, Seunggyu, Wan, Zhengpeng, Jeon, Jessie S. and Kamm, Roger D. 2022. "Microfluidic vascular models of tumor cell extravasation." 12. 10.3389/fonc.2022.1052192 Creative Commons Attribution 4.0 International license https://creativecommons.org/licenses/by/4.0/ application/pdf Frontiers Media SA Frontiers
spellingShingle Cancer Research
Oncology
Kim, Seunggyu
Wan, Zhengpeng
Jeon, Jessie S.
Kamm, Roger D.
Microfluidic vascular models of tumor cell extravasation
title Microfluidic vascular models of tumor cell extravasation
title_full Microfluidic vascular models of tumor cell extravasation
title_fullStr Microfluidic vascular models of tumor cell extravasation
title_full_unstemmed Microfluidic vascular models of tumor cell extravasation
title_short Microfluidic vascular models of tumor cell extravasation
title_sort microfluidic vascular models of tumor cell extravasation
topic Cancer Research
Oncology
url https://hdl.handle.net/1721.1/146568
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AT wanzhengpeng microfluidicvascularmodelsoftumorcellextravasation
AT jeonjessies microfluidicvascularmodelsoftumorcellextravasation
AT kammrogerd microfluidicvascularmodelsoftumorcellextravasation