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The SW480 cell line as a model of resident and migrating colon cancer stem cells.
Verhagen, Mathijs P; Xu, Tong; Stabile, Roberto; Joosten, Rosalie; Tucci, Francesco A; van Royen, Martin; Trerotola, Marco; Alberti, Saverio; Sacchetti, Andrea; Fodde, Riccardo.
Afiliação
  • Verhagen MP; Department of Pathology, Erasmus University Medical Center, Rotterdam, the Netherlands.
  • Xu T; Department of Pathology, Erasmus University Medical Center, Rotterdam, the Netherlands.
  • Stabile R; Department of Pathology, Erasmus University Medical Center, Rotterdam, the Netherlands.
  • Joosten R; Department of Pathology, Erasmus University Medical Center, Rotterdam, the Netherlands.
  • Tucci FA; Department of Pathology, Erasmus University Medical Center, Rotterdam, the Netherlands.
  • van Royen M; Department of Pathology, Erasmus University Medical Center, Rotterdam, the Netherlands.
  • Trerotola M; Department of Medical, Oral and Biotechnological Sciences, University of Chieti-Pescara, Chieti, Italy.
  • Alberti S; Department of Biomedical Sciences, University of Messina, Messina, Italy.
  • Sacchetti A; Department of Pathology, Erasmus University Medical Center, Rotterdam, the Netherlands.
  • Fodde R; Department of Pathology, Erasmus University Medical Center, Rotterdam, the Netherlands.
iScience ; 27(9): 110658, 2024 Sep 20.
Article em En | MEDLINE | ID: mdl-39246444
ABSTRACT
Intra-tumor heterogeneity, i.e., the presence of diverse cell types and subpopulations within tumors, presents a significant obstacle in cancer treatment due to its negative consequences for resistance to therapy and disease recurrence. However, the mechanisms that underlie intra-tumor heterogeneity and result in the plethora of different cancer cells within a single lesion remain poorly understood. Here, we leverage the SW480 cell line as a model system to investigate the molecular and functional diversity of colon cancer cells. Through a combination of fluorescence-activated cell sorting (FACS) analysis and transcriptomic profiling, we identified three distinct subpopulations, namely resident cancer stem cells (rCSCs), migratory CSCs (mCSCs), and high-relapse cells (HRCs). These subpopulations show varying Wnt signaling levels and gene expression profiles mirroring their stem-like and functional properties. Examination of publicly available spatial transcriptomic data confirms the presence of these subpopulations in patient-derived cancers and reveals their distinct spatial distribution relative to the tumor microenvironment.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: IScience Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Holanda País de publicação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: IScience Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Holanda País de publicação: Estados Unidos