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Extensive characterization of sphere models established from colorectal cancer cell lines
Authors:Ada Collura  Laetitia Marisa  Diletta Trojan  Olivier Buhard  Anaïs Lagrange  Arnaud Saget  Marianne Bombled  Patricia Méchighel  Mira Ayadi  Martine Muleris  Aurélien de Reynies  Magali Svrcek  Jean-François Fléjou  Jean-Claude Florent  Florence Mahuteau-Betzer  Anne-Marie Faussat  Alex Duval
Institution:1. Inserm, UMRS_938, Centre de Recherche Saint-Antoine, Equipe “Instabilité des Microsatellites et Cancers”, 75012, Paris, France
2. Université Pierre et Marie Curie-Paris6, Paris, France
7. INSERM UMRS 938 Team “Microsatellite Instability and Cancer”, H?pital Saint-Antoine, 184, rue du Faubourg Saint-Antoine, 75571, Paris cedex 12, France
3. Programme “Cartes d’Identité des Tumeurs”, Ligue Nationale Contre le Cancer, Paris, France
4. UMR 176 CNRS/Institut Curie, Universite Paris-Sud, Orsay, France
5. AP-HP, H?pital Saint-Antoine, Service d’Anatomie et Cytologie Pathologiques, Paris, France
6. AP-HP, H?pital Saint-Antoine, Tumorothèque CancerEst, 75012, Paris, France
Abstract:Links between cancer and stem cells have been proposed for many years. As the cancer stem cell (CSC) theory became widely studied, new methods were developed to culture and expand cancer cells with conserved determinants of “stemness”. These cells show increased ability to grow in suspension as spheres in serum-free medium supplemented with growth factors and chemicals. The physiological relevance of this phenomenon in established cancer cell lines remains unclear. Cell lines have traditionally been used to explore tumor biology and serve as preclinical models for the screening of potential therapeutic agents. Here, we grew cell-forming spheres (CFS) from 25 established colorectal cancer cell lines. The molecular and cellular characteristics of CFS were compared to the bulk of tumor cells. CFS could be isolated from 72 % of the cell lines. Both CFS and their parental CRC cell lines were highly tumorigenic. Compared to their parental cells, they showed similar expression of putative CSC markers. The ability of CRC cells to grow as CFS was greatly enhanced by prior treatment with 5-fluorouracil. At the molecular level, CFS and parental CRC cells showed identical gene mutations and very similar genomic profiles, although microarray analysis revealed changes in CFS gene expression that were independent of DNA copy-number. We identified a CFS gene expression signature common to CFS from all CRC cell lines, which was predictive of disease relapse in CRC patients. In conclusion, CFS models derived from CRC cell lines possess interesting phenotypic features that may have clinical relevance for drug resistance and disease relapse.
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