Cocultures of Mesenchymal Stem Cells and Endothelial Cells As Organotypic Models of Prostate Cancer Metastasis
In spite of recognized limitations in capturing species-specific responses and high costs, rodent models remain commonly used in prostate cancer metastasis research, due largely to the lack of available alternatives. We aim to develop an in vitro culture system to study prostate cancer response to a...
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sg-ntu-dr.10356-823702023-12-29T06:45:12Z Cocultures of Mesenchymal Stem Cells and Endothelial Cells As Organotypic Models of Prostate Cancer Metastasis Chong, Mark Seow Khoon Lim, Jing Goh, Junwei Sia, Ming Wei Teoh, Swee Hin Chan, Jerry Kok Yen School of Chemical and Biomedical Engineering Prostate cancer In-vitro model Metastasis Bone Microenvironment Organotypic In spite of recognized limitations in capturing species-specific responses and high costs, rodent models remain commonly used in prostate cancer metastasis research, due largely to the lack of available alternatives. We aim to develop an in vitro culture system to study prostate cancer response to a simulated bone microenvironment, which may be used to understand early events in prostate metastasis to bone or for drug screening applications. To achieve this, mesenchymal stem cells and endothelial cells were isolated and cocultured to form a vascularized bone analogue. Endothelial cells were found to exert osteopotentiating effects on mesenchymal stem cell differentiation, and reciprocal effects by the stromal cells were found to stimulate vasculogenic responses, suggesting the possible utility of this system to elicit three-way interactions between endothelial, mesenchymal, and prostate cancer cells. We further developed the use of fluorescently labeled cells which could be used to concurrently track cellular migration, proliferation, and morphometric analysis. We demonstrate the concurrent, real-time visualization of prostate cancer and endothelial cells, which may be useful for evaluation of spatiotemporal changes at a single-cell level. When prostate cancer cell proliferation on various substrates was measured, it was found that the use of coculture systems may provide a better reflection of conditions in vivo, highlighting the potential utility as a model system. NMRC (Natl Medical Research Council, S’pore) Accepted version 2016-02-23T02:50:52Z 2019-12-06T14:54:19Z 2016-02-23T02:50:52Z 2019-12-06T14:54:19Z 2014 Journal Article Chong, M. S. K., Lim, J., Goh, J., Sia, M. W., Chan, J. K. Y., & Teoh, S. H. (2014). Cocultures of Mesenchymal Stem Cells and Endothelial Cells As Organotypic Models of Prostate Cancer Metastasis. Molecular Pharmaceutics, 11(7), 2126-2133. 1543-8384 https://hdl.handle.net/10356/82370 http://hdl.handle.net/10220/40029 10.1021/mp500141b en Molecular Pharmaceutics © 2014 American Chemical Society. This is the author created version of a work that has been peer reviewed and accepted for publication by Molecular Pharmaceutics, American Chemical Society. It incorporates referee’s comments but changes resulting from the publishing process, such as copyediting, structural formatting, may not be reflected in this document. The published version is available at: [http://dx.doi.org/10.1021/mp500141b]. 25 p. application/pdf |
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Prostate cancer In-vitro model Metastasis Bone Microenvironment Organotypic Chong, Mark Seow Khoon Lim, Jing Goh, Junwei Sia, Ming Wei Teoh, Swee Hin Chan, Jerry Kok Yen Cocultures of Mesenchymal Stem Cells and Endothelial Cells As Organotypic Models of Prostate Cancer Metastasis |
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In spite of recognized limitations in capturing species-specific responses and high costs, rodent models remain commonly used in prostate cancer metastasis research, due largely to the lack of available alternatives. We aim to develop an in vitro culture system to study prostate cancer response to a simulated bone microenvironment, which may be used to understand early events in prostate metastasis to bone or for drug screening applications. To achieve this, mesenchymal stem cells and endothelial cells were isolated and cocultured to form a vascularized bone analogue. Endothelial cells were found to exert osteopotentiating effects on mesenchymal stem cell differentiation, and reciprocal effects by the stromal cells were found to stimulate vasculogenic responses, suggesting the possible utility of this system to elicit three-way interactions between endothelial, mesenchymal, and prostate cancer cells. We further developed the use of fluorescently labeled cells which could be used to concurrently track cellular migration, proliferation, and morphometric analysis. We demonstrate the concurrent, real-time visualization of prostate cancer and endothelial cells, which may be useful for evaluation of spatiotemporal changes at a single-cell level. When prostate cancer cell proliferation on various substrates was measured, it was found that the use of coculture systems may provide a better reflection of conditions in vivo, highlighting the potential utility as a model system. |
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School of Chemical and Biomedical Engineering |
author_facet |
School of Chemical and Biomedical Engineering Chong, Mark Seow Khoon Lim, Jing Goh, Junwei Sia, Ming Wei Teoh, Swee Hin Chan, Jerry Kok Yen |
format |
Article |
author |
Chong, Mark Seow Khoon Lim, Jing Goh, Junwei Sia, Ming Wei Teoh, Swee Hin Chan, Jerry Kok Yen |
author_sort |
Chong, Mark Seow Khoon |
title |
Cocultures of Mesenchymal Stem Cells and Endothelial Cells As Organotypic Models of Prostate Cancer Metastasis |
title_short |
Cocultures of Mesenchymal Stem Cells and Endothelial Cells As Organotypic Models of Prostate Cancer Metastasis |
title_full |
Cocultures of Mesenchymal Stem Cells and Endothelial Cells As Organotypic Models of Prostate Cancer Metastasis |
title_fullStr |
Cocultures of Mesenchymal Stem Cells and Endothelial Cells As Organotypic Models of Prostate Cancer Metastasis |
title_full_unstemmed |
Cocultures of Mesenchymal Stem Cells and Endothelial Cells As Organotypic Models of Prostate Cancer Metastasis |
title_sort |
cocultures of mesenchymal stem cells and endothelial cells as organotypic models of prostate cancer metastasis |
publishDate |
2016 |
url |
https://hdl.handle.net/10356/82370 http://hdl.handle.net/10220/40029 |
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1787136431970320384 |