Epithelial-to-mesenchymal Transition Heterogeneity of Circulating Tumor Cells and Their Correlation With MDSCs and Tregs in HER2-negative Metastatic Breast Cancer Patients.


Journal

Anticancer research
ISSN: 1791-7530
Titre abrégé: Anticancer Res
Pays: Greece
ID NLM: 8102988

Informations de publication

Date de publication:
Feb 2021
Historique:
received: 04 12 2020
revised: 03 01 2021
accepted: 14 01 2021
entrez: 31 1 2021
pubmed: 1 2 2021
medline: 9 2 2021
Statut: ppublish

Résumé

To investigate the correlation between circulating tumor cells (CTCs) bearing cancer stem cell (CSC) and epithelial-to-mesenchymal (EMT) phenotypes and the different immunosuppressive cells in peripheral blood of patients with metastatic breast cancer (mBC). Blood was obtained from 38 pre-treated patients with mBC before a new line of treatment. CTC detection and characterization was performed by triple immunofluorescent staining, while Myeloid-derived Suppressor Cells (MDSCs) and T regulatory cells (Tregs) were analyzed by multi-flow cytometry. CTCs were detected in 16 (42.1%) of patients. Based on the co-expression of ALDH1, TWIST and CK, CTCs revealed an important heterogeneity: CTCs with a CSC/partial-EMT, CSC/Epithelial-like, non-CSC/partial-EMT and non-CSC/Epithelial-like phenotype were detected in 7 (18.4%), 7 (18.4%), 1 (1.4%) and 9 (23.7%) of patients, respectively. Immunophenotyping of MDSCs identified 2 monocytic [M-MDSCs; CD14 These findings provide evidence that CTCs in ER

Sections du résumé

BACKGROUND BACKGROUND
To investigate the correlation between circulating tumor cells (CTCs) bearing cancer stem cell (CSC) and epithelial-to-mesenchymal (EMT) phenotypes and the different immunosuppressive cells in peripheral blood of patients with metastatic breast cancer (mBC).
MATERIALS AND METHODS METHODS
Blood was obtained from 38 pre-treated patients with mBC before a new line of treatment. CTC detection and characterization was performed by triple immunofluorescent staining, while Myeloid-derived Suppressor Cells (MDSCs) and T regulatory cells (Tregs) were analyzed by multi-flow cytometry.
RESULTS RESULTS
CTCs were detected in 16 (42.1%) of patients. Based on the co-expression of ALDH1, TWIST and CK, CTCs revealed an important heterogeneity: CTCs with a CSC/partial-EMT, CSC/Epithelial-like, non-CSC/partial-EMT and non-CSC/Epithelial-like phenotype were detected in 7 (18.4%), 7 (18.4%), 1 (1.4%) and 9 (23.7%) of patients, respectively. Immunophenotyping of MDSCs identified 2 monocytic [M-MDSCs; CD14
CONCLUSION CONCLUSIONS
These findings provide evidence that CTCs in ER

Identifiants

pubmed: 33517270
pii: 41/2/661
doi: 10.21873/anticanres.14817
doi:

Substances chimiques

Biomarkers, Tumor 0

Types de publication

Comparative Study Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

661-670

Informations de copyright

Copyright © 2021 International Institute of Anticancer Research (Dr. George J. Delinasios), All rights reserved.

Auteurs

Maria A Papadaki (MA)

Laboratory of Translational Oncology, School of Medicine, University of Crete, Heraklion, Greece.

Despoina Aggouraki (D)

Laboratory of Translational Oncology, School of Medicine, University of Crete, Heraklion, Greece.

Eleni-Kyriaki Vetsika (EK)

Laboratory of Translational Oncology, School of Medicine, University of Crete, Heraklion, Greece.

Nikolaos Xenidis (N)

Department of Medical Oncology, Medical School, Democritus University of Thrace, Alexandroupolis, Greece.
Hellenic Oncology Research Group (HORG), Athens, Greece.

Galaktea Kallergi (G)

Hellenic Oncology Research Group (HORG), Athens, Greece.
Department of Biology, University of Patras, Patras, Greece.

Athanasios Kotsakis (A)

Hellenic Oncology Research Group (HORG), Athens, Greece.
Department of Medical Oncology, University Hospital of Larissa & Laboratory of Oncology, Faculty of Medicine, School of Health Sciences, University of Thessaly, Larissa, Greece.

Vassilis Georgoulias (V)

Hellenic Oncology Research Group (HORG), Athens, Greece; georgulv@otenet.gr.
School of Medicine, University of Crete, Heraklion, Greece.

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Classifications MeSH