Isolation and Characterization of Two Novel Colorectal Cancer Cell Lines, Containing a Subpopulation with Potential Stem-Like Properties: Treatment Options by MYC/NMYC Inhibition.

ATRA EMT KJ-Pyr-9 MYC NMYC colorectal adenocarcinoma colorectal cancer stem cells rectal neuroendocrine carcinoma

Journal

Cancers
ISSN: 2072-6694
Titre abrégé: Cancers (Basel)
Pays: Switzerland
ID NLM: 101526829

Informations de publication

Date de publication:
10 Sep 2020
Historique:
received: 14 08 2020
revised: 04 09 2020
accepted: 08 09 2020
entrez: 15 9 2020
pubmed: 16 9 2020
medline: 16 9 2020
Statut: epublish

Résumé

Cancer stem cells (CSC) are crucial mediators of cancer relapse. Here, we isolated two primary human colorectal cancer cell lines derived from a rectal neuroendocrine carcinoma (BKZ-2) and a colorectal adenocarcinoma (BKZ-3), both containing subpopulations with potential stem-like properties. Protein expression of CSC-markers prominin-1 and CD44 antigen was significantly higher for BKZ-2 and BKZ-3 in comparison to well-established colon carcinoma cell lines. High sphere-formation capacity further confirmed the existence of a subpopulation with potential stem-like phenotype. Epithelial-mesenchymal transition markers as well as immune checkpoint ligands were expressed more pronounced in BKZ-2. Both cell populations demonstrated N-myc proto-oncogene (

Identifiants

pubmed: 32927768
pii: cancers12092582
doi: 10.3390/cancers12092582
pmc: PMC7564713
pii:
doi:

Types de publication

Journal Article

Langues

eng

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Auteurs

Jan Schulte Am Schulte Am Esch (JSA)

Department of General and Visceral Surgery, Protestant Hospital of Bethel Foundation, 33611 Bielefeld, Germany.
Forschungsverbund BioMedizin Bielefeld (FBMB), 33611 Bielefeld, Germany.

Beatrice Ariane Windmöller (BA)

Forschungsverbund BioMedizin Bielefeld (FBMB), 33611 Bielefeld, Germany.
Department of Cell Biology, University of Bielefeld, 33611 Bielefeld, Germany.

Johannes Hanewinkel (J)

Department of Cell Biology, University of Bielefeld, 33611 Bielefeld, Germany.

Jonathan Storm (J)

Forschungsverbund BioMedizin Bielefeld (FBMB), 33611 Bielefeld, Germany.
Department of Cell Biology, University of Bielefeld, 33611 Bielefeld, Germany.

Christine Förster (C)

Forschungsverbund BioMedizin Bielefeld (FBMB), 33611 Bielefeld, Germany.
Institute of Pathology, KRH Hospital Nordstadt, affiliated with the Protestant Hospital of Bethel Foundation, 30167 Hannover, Germany.

Ludwig Wilkens (L)

Forschungsverbund BioMedizin Bielefeld (FBMB), 33611 Bielefeld, Germany.
Institute of Pathology, KRH Hospital Nordstadt, affiliated with the Protestant Hospital of Bethel Foundation, 30167 Hannover, Germany.

Martin Krüger (M)

Forschungsverbund BioMedizin Bielefeld (FBMB), 33611 Bielefeld, Germany.
Department of Internal Medicine and Gastroenterology, Protestant Hospital of Bethel Foundation, 33611 Bielefeld, Germany.

Barbara Kaltschmidt (B)

Forschungsverbund BioMedizin Bielefeld (FBMB), 33611 Bielefeld, Germany.
Department of Cell Biology, University of Bielefeld, 33611 Bielefeld, Germany.
Molecular Neurobiology, University of Bielefeld, 33615 Bielefeld, Germany.

Christian Kaltschmidt (C)

Forschungsverbund BioMedizin Bielefeld (FBMB), 33611 Bielefeld, Germany.
Department of Cell Biology, University of Bielefeld, 33611 Bielefeld, Germany.

Classifications MeSH