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

Authors :
Dangles-Marie
Ivan Bièche
Sophie Richon
Louis-Bastien Weiswald
Sophie Vacher
Pierre Validire
Gérald Massonnet
Paul-Henri Cottu
Elisabetta Marangoni
Fariba Nemati
Dominique Bellet
J.-M. Guinebretiere
Ingrid Laurendeau
Source :
British Journal of Cancer
Publication Year :
2013
Publisher :
Springer Science and Business Media LLC, 2013.

Abstract

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.

Details

ISSN :
15321827 and 00070920
Volume :
108
Database :
OpenAIRE
Journal :
British Journal of Cancer
Accession number :
edsair.doi.dedup.....6028c5eaa74f5db559eee04a04ac2e16