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Identification of RSK and TTK as Modulators of Blood Vessel Morphogenesis Using an Embryonic Stem Cell-Based Vascular Differentiation Assay

Blood vessels are formed through vasculogenesis, followed by remodeling of the endothelial network through angiogenesis. Many events that occur during embryonic vascular development are recapitulated during adult neoangiogenesis, which is critical to tumor growth and metastasis. Current antiangiogen...

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Autores principales: Hammoud, Lamis, Adams, Jessica R., Loch, Amanda J., Marcellus, Richard C., Uehling, David E., Aman, Ahmed, Fladd, Christopher, McKee, Trevor D., Jo, Christine E.B., Al-Awar, Rima, Egan, Sean E., Rossant, Janet
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5063585/
https://www.ncbi.nlm.nih.gov/pubmed/27618721
http://dx.doi.org/10.1016/j.stemcr.2016.08.004
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author Hammoud, Lamis
Adams, Jessica R.
Loch, Amanda J.
Marcellus, Richard C.
Uehling, David E.
Aman, Ahmed
Fladd, Christopher
McKee, Trevor D.
Jo, Christine E.B.
Al-Awar, Rima
Egan, Sean E.
Rossant, Janet
author_facet Hammoud, Lamis
Adams, Jessica R.
Loch, Amanda J.
Marcellus, Richard C.
Uehling, David E.
Aman, Ahmed
Fladd, Christopher
McKee, Trevor D.
Jo, Christine E.B.
Al-Awar, Rima
Egan, Sean E.
Rossant, Janet
author_sort Hammoud, Lamis
collection PubMed
description Blood vessels are formed through vasculogenesis, followed by remodeling of the endothelial network through angiogenesis. Many events that occur during embryonic vascular development are recapitulated during adult neoangiogenesis, which is critical to tumor growth and metastasis. Current antiangiogenic tumor therapies, based largely on targeting the vascular endothelial growth factor pathway, show limited clinical benefits, thus necessitating the discovery of alternative targets. Here we report the development of a robust embryonic stem cell-based vascular differentiation assay amenable to small-molecule screens to identify novel modulators of angiogenesis. In this context, RSK and TTK were identified as angiogenic modulators. Inhibition of these pathways inhibited angiogenesis in embryoid bodies and human umbilical vein endothelial cells. Furthermore, inhibition of RSK and TTK reduced tumor growth, vascular density, and improved survival in an in vivo Lewis lung carcinoma mouse model. Our study suggests that RSK and TTK are potential targets for antiangiogenic therapy, and provides an assay system for further pathway screens.
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spelling pubmed-50635852016-10-19 Identification of RSK and TTK as Modulators of Blood Vessel Morphogenesis Using an Embryonic Stem Cell-Based Vascular Differentiation Assay Hammoud, Lamis Adams, Jessica R. Loch, Amanda J. Marcellus, Richard C. Uehling, David E. Aman, Ahmed Fladd, Christopher McKee, Trevor D. Jo, Christine E.B. Al-Awar, Rima Egan, Sean E. Rossant, Janet Stem Cell Reports Resource Blood vessels are formed through vasculogenesis, followed by remodeling of the endothelial network through angiogenesis. Many events that occur during embryonic vascular development are recapitulated during adult neoangiogenesis, which is critical to tumor growth and metastasis. Current antiangiogenic tumor therapies, based largely on targeting the vascular endothelial growth factor pathway, show limited clinical benefits, thus necessitating the discovery of alternative targets. Here we report the development of a robust embryonic stem cell-based vascular differentiation assay amenable to small-molecule screens to identify novel modulators of angiogenesis. In this context, RSK and TTK were identified as angiogenic modulators. Inhibition of these pathways inhibited angiogenesis in embryoid bodies and human umbilical vein endothelial cells. Furthermore, inhibition of RSK and TTK reduced tumor growth, vascular density, and improved survival in an in vivo Lewis lung carcinoma mouse model. Our study suggests that RSK and TTK are potential targets for antiangiogenic therapy, and provides an assay system for further pathway screens. Elsevier 2016-09-08 /pmc/articles/PMC5063585/ /pubmed/27618721 http://dx.doi.org/10.1016/j.stemcr.2016.08.004 Text en © 2016 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Resource
Hammoud, Lamis
Adams, Jessica R.
Loch, Amanda J.
Marcellus, Richard C.
Uehling, David E.
Aman, Ahmed
Fladd, Christopher
McKee, Trevor D.
Jo, Christine E.B.
Al-Awar, Rima
Egan, Sean E.
Rossant, Janet
Identification of RSK and TTK as Modulators of Blood Vessel Morphogenesis Using an Embryonic Stem Cell-Based Vascular Differentiation Assay
title Identification of RSK and TTK as Modulators of Blood Vessel Morphogenesis Using an Embryonic Stem Cell-Based Vascular Differentiation Assay
title_full Identification of RSK and TTK as Modulators of Blood Vessel Morphogenesis Using an Embryonic Stem Cell-Based Vascular Differentiation Assay
title_fullStr Identification of RSK and TTK as Modulators of Blood Vessel Morphogenesis Using an Embryonic Stem Cell-Based Vascular Differentiation Assay
title_full_unstemmed Identification of RSK and TTK as Modulators of Blood Vessel Morphogenesis Using an Embryonic Stem Cell-Based Vascular Differentiation Assay
title_short Identification of RSK and TTK as Modulators of Blood Vessel Morphogenesis Using an Embryonic Stem Cell-Based Vascular Differentiation Assay
title_sort identification of rsk and ttk as modulators of blood vessel morphogenesis using an embryonic stem cell-based vascular differentiation assay
topic Resource
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5063585/
https://www.ncbi.nlm.nih.gov/pubmed/27618721
http://dx.doi.org/10.1016/j.stemcr.2016.08.004
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