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Basement Membrane-Rich Organoids with Functional Human Blood Vessels Are Permissive Niches for Human Breast Cancer Metastasis

Metastasic breast cancer is the leading cause of death by malignancy in women worldwide. Tumor metastasis is a multistep process encompassing local invasion of cancer cells at primary tumor site, intravasation into the blood vessel, survival in systemic circulation, and extravasation across the endo...

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Autores principales: Fernández-Periáñez, Rodrigo, Molina-Privado, Irene, Rojo, Federico, Guijarro-Muñoz, Irene, Alonso-Camino, Vanesa, Zazo, Sandra, Compte, Marta, Álvarez-Cienfuegos, Ana, Cuesta, Ángel M., Sánchez-Martín, David, Álvarez-Méndez, Ana M., Sanz, Laura, Álvarez-Vallina, Luis
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3738545/
https://www.ncbi.nlm.nih.gov/pubmed/23951338
http://dx.doi.org/10.1371/journal.pone.0072957
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author Fernández-Periáñez, Rodrigo
Molina-Privado, Irene
Rojo, Federico
Guijarro-Muñoz, Irene
Alonso-Camino, Vanesa
Zazo, Sandra
Compte, Marta
Álvarez-Cienfuegos, Ana
Cuesta, Ángel M.
Sánchez-Martín, David
Álvarez-Méndez, Ana M.
Sanz, Laura
Álvarez-Vallina, Luis
author_facet Fernández-Periáñez, Rodrigo
Molina-Privado, Irene
Rojo, Federico
Guijarro-Muñoz, Irene
Alonso-Camino, Vanesa
Zazo, Sandra
Compte, Marta
Álvarez-Cienfuegos, Ana
Cuesta, Ángel M.
Sánchez-Martín, David
Álvarez-Méndez, Ana M.
Sanz, Laura
Álvarez-Vallina, Luis
author_sort Fernández-Periáñez, Rodrigo
collection PubMed
description Metastasic breast cancer is the leading cause of death by malignancy in women worldwide. Tumor metastasis is a multistep process encompassing local invasion of cancer cells at primary tumor site, intravasation into the blood vessel, survival in systemic circulation, and extravasation across the endothelium to metastasize at a secondary site. However, only a small percentage of circulating cancer cells initiate metastatic colonies. This fact, together with the inaccessibility and structural complexity of target tissues has hampered the study of the later steps in cancer metastasis. In addition, most data are derived from in vivo models where critical steps such as intravasation/extravasation of human cancer cells are mediated by murine endothelial cells. Here, we developed a new mouse model to study the molecular and cellular mechanisms underlying late steps of the metastatic cascade. We have shown that a network of functional human blood vessels can be formed by co-implantation of human endothelial cells and mesenchymal cells, embedded within a reconstituted basement membrane-like matrix and inoculated subcutaneously into immunodeficient mice. The ability of circulating cancer cells to colonize these human vascularized organoids was next assessed in an orthotopic model of human breast cancer by bioluminescent imaging, molecular techniques and immunohistological analysis. We demonstrate that disseminated human breast cancer cells efficiently colonize organoids containing a functional microvessel network composed of human endothelial cells, connected to the mouse circulatory system. Human breast cancer cells could be clearly detected at different stages of the metastatic process: initial arrest in the human microvasculature, extravasation, and growth into avascular micrometastases. This new mouse model may help us to map the extravasation process with unprecedented detail, opening the way for the identification of relevant targets for therapeutic intervention.
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spelling pubmed-37385452013-08-15 Basement Membrane-Rich Organoids with Functional Human Blood Vessels Are Permissive Niches for Human Breast Cancer Metastasis Fernández-Periáñez, Rodrigo Molina-Privado, Irene Rojo, Federico Guijarro-Muñoz, Irene Alonso-Camino, Vanesa Zazo, Sandra Compte, Marta Álvarez-Cienfuegos, Ana Cuesta, Ángel M. Sánchez-Martín, David Álvarez-Méndez, Ana M. Sanz, Laura Álvarez-Vallina, Luis PLoS One Research Article Metastasic breast cancer is the leading cause of death by malignancy in women worldwide. Tumor metastasis is a multistep process encompassing local invasion of cancer cells at primary tumor site, intravasation into the blood vessel, survival in systemic circulation, and extravasation across the endothelium to metastasize at a secondary site. However, only a small percentage of circulating cancer cells initiate metastatic colonies. This fact, together with the inaccessibility and structural complexity of target tissues has hampered the study of the later steps in cancer metastasis. In addition, most data are derived from in vivo models where critical steps such as intravasation/extravasation of human cancer cells are mediated by murine endothelial cells. Here, we developed a new mouse model to study the molecular and cellular mechanisms underlying late steps of the metastatic cascade. We have shown that a network of functional human blood vessels can be formed by co-implantation of human endothelial cells and mesenchymal cells, embedded within a reconstituted basement membrane-like matrix and inoculated subcutaneously into immunodeficient mice. The ability of circulating cancer cells to colonize these human vascularized organoids was next assessed in an orthotopic model of human breast cancer by bioluminescent imaging, molecular techniques and immunohistological analysis. We demonstrate that disseminated human breast cancer cells efficiently colonize organoids containing a functional microvessel network composed of human endothelial cells, connected to the mouse circulatory system. Human breast cancer cells could be clearly detected at different stages of the metastatic process: initial arrest in the human microvasculature, extravasation, and growth into avascular micrometastases. This new mouse model may help us to map the extravasation process with unprecedented detail, opening the way for the identification of relevant targets for therapeutic intervention. Public Library of Science 2013-08-08 /pmc/articles/PMC3738545/ /pubmed/23951338 http://dx.doi.org/10.1371/journal.pone.0072957 Text en © 2013 Fernández-Periañez et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Fernández-Periáñez, Rodrigo
Molina-Privado, Irene
Rojo, Federico
Guijarro-Muñoz, Irene
Alonso-Camino, Vanesa
Zazo, Sandra
Compte, Marta
Álvarez-Cienfuegos, Ana
Cuesta, Ángel M.
Sánchez-Martín, David
Álvarez-Méndez, Ana M.
Sanz, Laura
Álvarez-Vallina, Luis
Basement Membrane-Rich Organoids with Functional Human Blood Vessels Are Permissive Niches for Human Breast Cancer Metastasis
title Basement Membrane-Rich Organoids with Functional Human Blood Vessels Are Permissive Niches for Human Breast Cancer Metastasis
title_full Basement Membrane-Rich Organoids with Functional Human Blood Vessels Are Permissive Niches for Human Breast Cancer Metastasis
title_fullStr Basement Membrane-Rich Organoids with Functional Human Blood Vessels Are Permissive Niches for Human Breast Cancer Metastasis
title_full_unstemmed Basement Membrane-Rich Organoids with Functional Human Blood Vessels Are Permissive Niches for Human Breast Cancer Metastasis
title_short Basement Membrane-Rich Organoids with Functional Human Blood Vessels Are Permissive Niches for Human Breast Cancer Metastasis
title_sort basement membrane-rich organoids with functional human blood vessels are permissive niches for human breast cancer metastasis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3738545/
https://www.ncbi.nlm.nih.gov/pubmed/23951338
http://dx.doi.org/10.1371/journal.pone.0072957
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