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An in vitro 3D bone metastasis model by using a human bone tissue culture and human sex-related cancer cells
One of the main limitations, when studying cancer-bone metastasis, is the complex nature of the native bone environment and the lack of reliable, simple, inexpensive models that closely mimic the biological processes occurring in patients and allowing the correct translation of results. To enhance t...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5363563/ https://www.ncbi.nlm.nih.gov/pubmed/27765913 http://dx.doi.org/10.18632/oncotarget.12763 |
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author | Salamanna, Francesca Borsari, Veronica Brogini, Silvia Giavaresi, Gianluca Parrilli, Annapaola Cepollaro, Simona Cadossi, Matteo Martini, Lucia Mazzotti, Antonio Fini, Milena |
author_facet | Salamanna, Francesca Borsari, Veronica Brogini, Silvia Giavaresi, Gianluca Parrilli, Annapaola Cepollaro, Simona Cadossi, Matteo Martini, Lucia Mazzotti, Antonio Fini, Milena |
author_sort | Salamanna, Francesca |
collection | PubMed |
description | One of the main limitations, when studying cancer-bone metastasis, is the complex nature of the native bone environment and the lack of reliable, simple, inexpensive models that closely mimic the biological processes occurring in patients and allowing the correct translation of results. To enhance the understanding of the mechanisms underlying human bone metastases and in order to find new therapies, we developed an in vitro three-dimensional (3D) cancer-bone metastasis model by culturing human breast or prostate cancer cells with human bone tissue isolated from female and male patients, respectively. Bone tissue discarded from total hip replacement surgery was cultured in a rolling apparatus system in a normoxic or hypoxic environment. Gene expression profile, protein levels, histological, immunohistochemical and four-dimensional (4D) micro-CT analyses showed a noticeable specificity of breast and prostate cancer cells for bone colonization and ingrowth, thus highlighting the species-specific and sex-specific osteotropism and the need to widen the current knowledge on cancer-bone metastasis spread in human bone tissues. The results of this study support the application of this model in preclinical studies on bone metastases and also follow the 3R principles, the guiding principles, aimed at replacing/reducing/refining (3R) animal use and their suffering for scientific purposes. |
format | Online Article Text |
id | pubmed-5363563 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-53635632017-03-29 An in vitro 3D bone metastasis model by using a human bone tissue culture and human sex-related cancer cells Salamanna, Francesca Borsari, Veronica Brogini, Silvia Giavaresi, Gianluca Parrilli, Annapaola Cepollaro, Simona Cadossi, Matteo Martini, Lucia Mazzotti, Antonio Fini, Milena Oncotarget Research Paper One of the main limitations, when studying cancer-bone metastasis, is the complex nature of the native bone environment and the lack of reliable, simple, inexpensive models that closely mimic the biological processes occurring in patients and allowing the correct translation of results. To enhance the understanding of the mechanisms underlying human bone metastases and in order to find new therapies, we developed an in vitro three-dimensional (3D) cancer-bone metastasis model by culturing human breast or prostate cancer cells with human bone tissue isolated from female and male patients, respectively. Bone tissue discarded from total hip replacement surgery was cultured in a rolling apparatus system in a normoxic or hypoxic environment. Gene expression profile, protein levels, histological, immunohistochemical and four-dimensional (4D) micro-CT analyses showed a noticeable specificity of breast and prostate cancer cells for bone colonization and ingrowth, thus highlighting the species-specific and sex-specific osteotropism and the need to widen the current knowledge on cancer-bone metastasis spread in human bone tissues. The results of this study support the application of this model in preclinical studies on bone metastases and also follow the 3R principles, the guiding principles, aimed at replacing/reducing/refining (3R) animal use and their suffering for scientific purposes. Impact Journals LLC 2016-10-19 /pmc/articles/PMC5363563/ /pubmed/27765913 http://dx.doi.org/10.18632/oncotarget.12763 Text en Copyright: © 2016 Salamanna et al. http://creativecommons.org/licenses/by/3.0/ 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 credited. |
spellingShingle | Research Paper Salamanna, Francesca Borsari, Veronica Brogini, Silvia Giavaresi, Gianluca Parrilli, Annapaola Cepollaro, Simona Cadossi, Matteo Martini, Lucia Mazzotti, Antonio Fini, Milena An in vitro 3D bone metastasis model by using a human bone tissue culture and human sex-related cancer cells |
title | An in vitro 3D bone metastasis model by using a human bone tissue culture and human sex-related cancer cells |
title_full | An in vitro 3D bone metastasis model by using a human bone tissue culture and human sex-related cancer cells |
title_fullStr | An in vitro 3D bone metastasis model by using a human bone tissue culture and human sex-related cancer cells |
title_full_unstemmed | An in vitro 3D bone metastasis model by using a human bone tissue culture and human sex-related cancer cells |
title_short | An in vitro 3D bone metastasis model by using a human bone tissue culture and human sex-related cancer cells |
title_sort | in vitro 3d bone metastasis model by using a human bone tissue culture and human sex-related cancer cells |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5363563/ https://www.ncbi.nlm.nih.gov/pubmed/27765913 http://dx.doi.org/10.18632/oncotarget.12763 |
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