The C-X-C Motif Chemokine Ligand 1 Sustains Breast Cancer Stem Cell Self-Renewal and Promotes Tumor Progression and Immune Escape Programs.

CXCL1 breast cancer stem cells chemokines immunity genes triple-negative breast cancer tumor microenvironment

Journal

Frontiers in cell and developmental biology
ISSN: 2296-634X
Titre abrégé: Front Cell Dev Biol
Pays: Switzerland
ID NLM: 101630250

Informations de publication

Date de publication:
2021
Historique:
received: 31 03 2021
accepted: 17 05 2021
entrez: 1 7 2021
pubmed: 2 7 2021
medline: 2 7 2021
Statut: epublish

Résumé

Breast cancer (BC) mortality is mainly due to metastatic disease, which is primarily driven by cancer stem cells (CSC). The chemokine C-X-C motif ligand-1 (CXCL1) is involved in BC metastasis, but the question of whether it regulates breast cancer stem cell (BCSC) behavior is yet to be explored. Here, we demonstrate that BCSCs express CXCR2 and produce CXCL1, which stimulates their proliferation and self-renewal, and that CXCL1 blockade inhibits both BCSC proliferation and mammosphere formation efficiency. CXCL1 amplifies its own production and remarkably induces both tumor-promoting and immunosuppressive factors, including

Identifiants

pubmed: 34195201
doi: 10.3389/fcell.2021.689286
pmc: PMC8237942
doi:

Types de publication

Journal Article

Langues

eng

Pagination

689286

Informations de copyright

Copyright © 2021 Ciummo, D’Antonio, Sorrentino, Fieni, Lanuti, Stassi, Todaro and Di Carlo.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Auteurs

Stefania Livia Ciummo (SL)

Department of Medicine and Sciences of Aging, "G. d'Annunzio" University, Chieti, Italy.
Anatomic Pathology and Immuno-Oncology Unit, Center for Advanced Studies and Technology (CAST), "G. d'Annunzio" University, Chieti, Italy.

Luigi D'Antonio (L)

Department of Medicine and Sciences of Aging, "G. d'Annunzio" University, Chieti, Italy.
Anatomic Pathology and Immuno-Oncology Unit, Center for Advanced Studies and Technology (CAST), "G. d'Annunzio" University, Chieti, Italy.

Carlo Sorrentino (C)

Department of Medicine and Sciences of Aging, "G. d'Annunzio" University, Chieti, Italy.
Anatomic Pathology and Immuno-Oncology Unit, Center for Advanced Studies and Technology (CAST), "G. d'Annunzio" University, Chieti, Italy.

Cristiano Fieni (C)

Department of Medicine and Sciences of Aging, "G. d'Annunzio" University, Chieti, Italy.
Anatomic Pathology and Immuno-Oncology Unit, Center for Advanced Studies and Technology (CAST), "G. d'Annunzio" University, Chieti, Italy.

Paola Lanuti (P)

Department of Medicine and Sciences of Aging, "G. d'Annunzio" University, Chieti, Italy.

Giorgio Stassi (G)

Department of Surgical, Oncological and Stomatological Sciences (DICHIRONS), University of Palermo, Palermo, Italy.

Matilde Todaro (M)

Department of Health Promotion Sciences, Internal Medicine and Medical Specialties (PROMISE), University of Palermo, Palermo, Italy.

Emma Di Carlo (E)

Department of Medicine and Sciences of Aging, "G. d'Annunzio" University, Chieti, Italy.
Anatomic Pathology and Immuno-Oncology Unit, Center for Advanced Studies and Technology (CAST), "G. d'Annunzio" University, Chieti, Italy.

Classifications MeSH