IL-8 and CXCR1 expression is associated with cancer stem cell-like properties of clear cell renal cancer.


Journal

The Journal of pathology
ISSN: 1096-9896
Titre abrégé: J Pathol
Pays: England
ID NLM: 0204634

Informations de publication

Date de publication:
07 2019
Historique:
received: 27 09 2018
revised: 25 02 2019
accepted: 13 03 2019
pubmed: 19 3 2019
medline: 9 4 2020
entrez: 19 3 2019
Statut: ppublish

Résumé

Recent studies suggest that clear cell renal cell carcinoma (ccRCC) possesses a rare population of cancer stem cells (CSCs) that might contribute to tumor heterogeneity, metastasis and therapeutic resistance. Nevertheless, their relevance for renal cancer is still unclear. In this study, we successfully isolated CSCs from established human ccRCC cell lines. CSCs displayed high expression of the chemokine IL-8 and its receptor CXCR1. While recombinant IL-8 significantly increased CSC number and properties in vitro, CXCR1 inhibition using an anti-CXCR1 antibody or repertaxin significantly reduced these features. After injection into immune-deficient mice, CSCs formed primary tumors that metastasized to the lung and liver. All xenografted tumors in mice expressed high levels of IL-8 and CXCR1. Furthermore, IL-8/CXCR1 expression significantly correlated with decreased overall survival in ccRCC patients. These results suggest that the IL-8/CXCR1 phenotype is associated with CSC-like properties in renal cancer. © 2019 The Authors. The Journal of Pathology published by John Wiley & Sons Ltd on behalf of Pathological Society of Great Britain and Ireland.

Identifiants

pubmed: 30883740
doi: 10.1002/path.5267
pmc: PMC6618115
doi:

Substances chimiques

Interleukin-8 0
Receptors, Interleukin-8A 0
Receptors, Interleukin-8B 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

377-389

Informations de copyright

© 2019 The Authors. The Journal of Pathology published by John Wiley & Sons Ltd on behalf of Pathological Society of Great Britain and Ireland.

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Auteurs

Claudia Corrò (C)

Department of Pathology and Molecular Pathology, University Hospital Zurich, Zurich, Switzerland.
Life Science Zurich Graduate School, ETH and University of Zurich, Zurich, Switzerland.

Marc E Healy (ME)

Department of Pathology and Molecular Pathology, University Hospital Zurich, Zurich, Switzerland.

Stefanie Engler (S)

Institute of Molecular Life Sciences, University of Zurich, Zurich, Switzerland.

Bernd Bodenmiller (B)

Institute of Molecular Life Sciences, University of Zurich, Zurich, Switzerland.

Zhe Li (Z)

Division of Genetics, Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, USA.

Peter Schraml (P)

Department of Pathology and Molecular Pathology, University Hospital Zurich, Zurich, Switzerland.

Achim Weber (A)

Department of Pathology and Molecular Pathology, University Hospital Zurich, Zurich, Switzerland.

Ian J Frew (IJ)

Clinic of Internal Medicine I, Faculty of Medicine, Medical Center - University of Freiburg, Freiburg im Breisgau, Germany.

Markus Rechsteiner (M)

Department of Pathology and Molecular Pathology, University Hospital Zurich, Zurich, Switzerland.

Holger Moch (H)

Department of Pathology and Molecular Pathology, University Hospital Zurich, Zurich, Switzerland.

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