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Novel Phenotypic Fluorescent Three-Dimensional Co-Culture Platforms for Recapitulating Tumor in vivo Progression and for Personalized Therapy

Because three-dimensional (3D) in vitro models are more accurate than 2D cell culture models and faster and cheaper than animal models, they have become a prospective trend in the biomedical and pharmaceutical fields, especially for personalized and targeted therapies. Because appropriate 3D models...

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Autores principales: Fang, Changge, Man, Yan-Gao, Cuttitta, Frank, Stetler-Stevenson, William, Salomon, David, Mazar, Andrew, Kulesza, Piotr, Rosen, Steve, Avital, Itzhak, Stojadinovic, Alexander, Jewett, Anahid, Jiang, Bin, Mulshine, James
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3842444/
https://www.ncbi.nlm.nih.gov/pubmed/24312145
http://dx.doi.org/10.7150/jca.7813
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author Fang, Changge
Man, Yan-Gao
Cuttitta, Frank
Stetler-Stevenson, William
Salomon, David
Mazar, Andrew
Kulesza, Piotr
Rosen, Steve
Avital, Itzhak
Stojadinovic, Alexander
Jewett, Anahid
Jiang, Bin
Mulshine, James
author_facet Fang, Changge
Man, Yan-Gao
Cuttitta, Frank
Stetler-Stevenson, William
Salomon, David
Mazar, Andrew
Kulesza, Piotr
Rosen, Steve
Avital, Itzhak
Stojadinovic, Alexander
Jewett, Anahid
Jiang, Bin
Mulshine, James
author_sort Fang, Changge
collection PubMed
description Because three-dimensional (3D) in vitro models are more accurate than 2D cell culture models and faster and cheaper than animal models, they have become a prospective trend in the biomedical and pharmaceutical fields, especially for personalized and targeted therapies. Because appropriate 3D models can be customized to mimic the in vivo microenvironment wherein various cell populations grow within an intricate but well organized extracellular matrix (ECM), they can accurately recapitulate physiological and pathophysiological progressions. The majority of cancers are carcinomas, which originate from epithelial cells, and dynamically interact with non-malignant cells including stromal cells (fibroblasts), vascular cells (endothelial cells and pericytes), immune cells (macrophages and mast cells), and the ECM. Employing a tumor monoclonal colony, tumor xenograft or patient cancer biopsy into an in vivo-like microenvironment, the native signaling pathways, cell-cell and cell-matrix interactions, and cell phenotypes are preserved and our fluorescent phenotypic 3D co-culture platforms can then accurately recapitulate the tumor in vivo scenario including tumor induced angiogenesis, tumor growth, and metastasis. In this paper, we describe a robust and standardized method to co-culture a tumor colony or biopsy with different cell populations, e.g., endothelial cells, immune cells, pericytes, etc. The procedures for recovering cells from the co-culture for molecular analyses, imaging, and analyzing are also described. We selected ECM solubilized extract derived from Engelbreth-Holm-Swam sarcoma cells. Because the 3D co-culture platforms can provide drug chemosensitivity data within 9 days that is equivalent to the results generated from mouse tumor xenograft models in 50 days, the 3D co-culture platforms are more accurate, efficient, and cost-effective and may replace animal models in the near future to predict drug efficacy, personalize therapies, prevent drug resistance, and improve the quality of life.
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spelling pubmed-38424442013-12-05 Novel Phenotypic Fluorescent Three-Dimensional Co-Culture Platforms for Recapitulating Tumor in vivo Progression and for Personalized Therapy Fang, Changge Man, Yan-Gao Cuttitta, Frank Stetler-Stevenson, William Salomon, David Mazar, Andrew Kulesza, Piotr Rosen, Steve Avital, Itzhak Stojadinovic, Alexander Jewett, Anahid Jiang, Bin Mulshine, James J Cancer Research Paper Because three-dimensional (3D) in vitro models are more accurate than 2D cell culture models and faster and cheaper than animal models, they have become a prospective trend in the biomedical and pharmaceutical fields, especially for personalized and targeted therapies. Because appropriate 3D models can be customized to mimic the in vivo microenvironment wherein various cell populations grow within an intricate but well organized extracellular matrix (ECM), they can accurately recapitulate physiological and pathophysiological progressions. The majority of cancers are carcinomas, which originate from epithelial cells, and dynamically interact with non-malignant cells including stromal cells (fibroblasts), vascular cells (endothelial cells and pericytes), immune cells (macrophages and mast cells), and the ECM. Employing a tumor monoclonal colony, tumor xenograft or patient cancer biopsy into an in vivo-like microenvironment, the native signaling pathways, cell-cell and cell-matrix interactions, and cell phenotypes are preserved and our fluorescent phenotypic 3D co-culture platforms can then accurately recapitulate the tumor in vivo scenario including tumor induced angiogenesis, tumor growth, and metastasis. In this paper, we describe a robust and standardized method to co-culture a tumor colony or biopsy with different cell populations, e.g., endothelial cells, immune cells, pericytes, etc. The procedures for recovering cells from the co-culture for molecular analyses, imaging, and analyzing are also described. We selected ECM solubilized extract derived from Engelbreth-Holm-Swam sarcoma cells. Because the 3D co-culture platforms can provide drug chemosensitivity data within 9 days that is equivalent to the results generated from mouse tumor xenograft models in 50 days, the 3D co-culture platforms are more accurate, efficient, and cost-effective and may replace animal models in the near future to predict drug efficacy, personalize therapies, prevent drug resistance, and improve the quality of life. Ivyspring International Publisher 2013-12-01 /pmc/articles/PMC3842444/ /pubmed/24312145 http://dx.doi.org/10.7150/jca.7813 Text en © Ivyspring International Publisher. This is an open-access article distributed under the terms of the Creative Commons License (http://creativecommons.org/licenses/by-nc-nd/3.0/). Reproduction is permitted for personal, noncommercial use, provided that the article is in whole, unmodified, and properly cited.
spellingShingle Research Paper
Fang, Changge
Man, Yan-Gao
Cuttitta, Frank
Stetler-Stevenson, William
Salomon, David
Mazar, Andrew
Kulesza, Piotr
Rosen, Steve
Avital, Itzhak
Stojadinovic, Alexander
Jewett, Anahid
Jiang, Bin
Mulshine, James
Novel Phenotypic Fluorescent Three-Dimensional Co-Culture Platforms for Recapitulating Tumor in vivo Progression and for Personalized Therapy
title Novel Phenotypic Fluorescent Three-Dimensional Co-Culture Platforms for Recapitulating Tumor in vivo Progression and for Personalized Therapy
title_full Novel Phenotypic Fluorescent Three-Dimensional Co-Culture Platforms for Recapitulating Tumor in vivo Progression and for Personalized Therapy
title_fullStr Novel Phenotypic Fluorescent Three-Dimensional Co-Culture Platforms for Recapitulating Tumor in vivo Progression and for Personalized Therapy
title_full_unstemmed Novel Phenotypic Fluorescent Three-Dimensional Co-Culture Platforms for Recapitulating Tumor in vivo Progression and for Personalized Therapy
title_short Novel Phenotypic Fluorescent Three-Dimensional Co-Culture Platforms for Recapitulating Tumor in vivo Progression and for Personalized Therapy
title_sort novel phenotypic fluorescent three-dimensional co-culture platforms for recapitulating tumor in vivo progression and for personalized therapy
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3842444/
https://www.ncbi.nlm.nih.gov/pubmed/24312145
http://dx.doi.org/10.7150/jca.7813
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