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A short-term colorectal cancer sphere culture as a relevant tool for human cancer biology investigation

BACKGROUND: Ex vivo colospheres have been previously characterised as a colorectal cancer (CRC) well-rounded multicellular model, exclusively formed by carcinoma cells, and derived from fresh CRC tissue after mechanical dissociation. The ability to form colospheres was correlated with tumour aggress...

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Autores principales: Weiswald, L-B, Richon, S, Massonnet, G, Guinebretière, J-M, Vacher, S, Laurendeau, I, Cottu, P, Marangoni, E, Nemati, F, Validire, P, Bellet, D, Bièche, I, Dangles-Marie, V
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3668460/
https://www.ncbi.nlm.nih.gov/pubmed/23538387
http://dx.doi.org/10.1038/bjc.2013.132
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author Weiswald, L-B
Richon, S
Massonnet, G
Guinebretière, J-M
Vacher, S
Laurendeau, I
Cottu, P
Marangoni, E
Nemati, F
Validire, P
Bellet, D
Bièche, I
Dangles-Marie, V
author_facet Weiswald, L-B
Richon, S
Massonnet, G
Guinebretière, J-M
Vacher, S
Laurendeau, I
Cottu, P
Marangoni, E
Nemati, F
Validire, P
Bellet, D
Bièche, I
Dangles-Marie, V
author_sort Weiswald, L-B
collection PubMed
description BACKGROUND: Ex vivo colospheres have been previously characterised as a colorectal cancer (CRC) well-rounded multicellular model, exclusively formed by carcinoma cells, and derived from fresh CRC tissue after mechanical dissociation. The ability to form colospheres was correlated with tumour aggressiveness. Their three-dimensional conformation prompted us to further investigate their potential interest as a preclinical cancer tool. METHODS: Patient-derived CRC xenografts were used to produce numerous colospheres. Mechanism of formation was elucidated by confocal microscopy. Expression analysis of a panel of 64 selected cancer-related genes by real-time qRT–PCR and hierarchical clustering allowed comparison of colospheres with parent xenografts. In vitro and in vivo assays were performed for migration and chemosensitivity studies. RESULTS: Colospheres, formed by tissue remodelling and compaction, remained viable several weeks in floating conditions, escaping anoikis through their strong cell–cell interactions. Colospheres matched the gene expression profile of the parent xenograft tissue. Colosphere-forming cells migrated in collagen I matrix and metastasised when subrenally implanted in nude mice. Besides, the colosphere responses to 5-fluorouracil and irinotecan, two standard drugs in CRC, reproduced those of the in vivo original xenografts. CONCLUSION: Colospheres closely mimic biological characteristics of in vivo CRC tumours. Consequently, they would be relevant ex vivo CRC models.
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spelling pubmed-36684602014-04-30 A short-term colorectal cancer sphere culture as a relevant tool for human cancer biology investigation Weiswald, L-B Richon, S Massonnet, G Guinebretière, J-M Vacher, S Laurendeau, I Cottu, P Marangoni, E Nemati, F Validire, P Bellet, D Bièche, I Dangles-Marie, V Br J Cancer Molecular Diagnostics BACKGROUND: Ex vivo colospheres have been previously characterised as a colorectal cancer (CRC) well-rounded multicellular model, exclusively formed by carcinoma cells, and derived from fresh CRC tissue after mechanical dissociation. The ability to form colospheres was correlated with tumour aggressiveness. Their three-dimensional conformation prompted us to further investigate their potential interest as a preclinical cancer tool. METHODS: Patient-derived CRC xenografts were used to produce numerous colospheres. Mechanism of formation was elucidated by confocal microscopy. Expression analysis of a panel of 64 selected cancer-related genes by real-time qRT–PCR and hierarchical clustering allowed comparison of colospheres with parent xenografts. In vitro and in vivo assays were performed for migration and chemosensitivity studies. RESULTS: Colospheres, formed by tissue remodelling and compaction, remained viable several weeks in floating conditions, escaping anoikis through their strong cell–cell interactions. Colospheres matched the gene expression profile of the parent xenograft tissue. Colosphere-forming cells migrated in collagen I matrix and metastasised when subrenally implanted in nude mice. Besides, the colosphere responses to 5-fluorouracil and irinotecan, two standard drugs in CRC, reproduced those of the in vivo original xenografts. CONCLUSION: Colospheres closely mimic biological characteristics of in vivo CRC tumours. Consequently, they would be relevant ex vivo CRC models. Nature Publishing Group 2013-04-30 2013-03-28 /pmc/articles/PMC3668460/ /pubmed/23538387 http://dx.doi.org/10.1038/bjc.2013.132 Text en Copyright © 2013 Cancer Research UK http://creativecommons.org/licenses/by-nc-sa/3.0/ From twelve months after its original publication, this work is licensed under the Creative Commons Attribution-NonCommercial-Share Alike 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/
spellingShingle Molecular Diagnostics
Weiswald, L-B
Richon, S
Massonnet, G
Guinebretière, J-M
Vacher, S
Laurendeau, I
Cottu, P
Marangoni, E
Nemati, F
Validire, P
Bellet, D
Bièche, I
Dangles-Marie, V
A short-term colorectal cancer sphere culture as a relevant tool for human cancer biology investigation
title A short-term colorectal cancer sphere culture as a relevant tool for human cancer biology investigation
title_full A short-term colorectal cancer sphere culture as a relevant tool for human cancer biology investigation
title_fullStr A short-term colorectal cancer sphere culture as a relevant tool for human cancer biology investigation
title_full_unstemmed A short-term colorectal cancer sphere culture as a relevant tool for human cancer biology investigation
title_short A short-term colorectal cancer sphere culture as a relevant tool for human cancer biology investigation
title_sort short-term colorectal cancer sphere culture as a relevant tool for human cancer biology investigation
topic Molecular Diagnostics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3668460/
https://www.ncbi.nlm.nih.gov/pubmed/23538387
http://dx.doi.org/10.1038/bjc.2013.132
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