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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Veröffentlicht in: | British journal of cancer 2013-04, Vol.108 (8), p.1720-1731 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | 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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ISSN: | 0007-0920 1532-1827 |
DOI: | 10.1038/bjc.2013.132 |