Immunoregulation and Clinical Implications of ANGPT2/TIE2


Journal

Cancer immunology research
ISSN: 2326-6074
Titre abrégé: Cancer Immunol Res
Pays: United States
ID NLM: 101614637

Informations de publication

Date de publication:
02 2020
Historique:
received: 03 05 2019
revised: 04 10 2019
accepted: 18 12 2019
pubmed: 25 12 2019
medline: 30 9 2020
entrez: 25 12 2019
Statut: ppublish

Résumé

Myeloid-derived suppressor cells (MDSC) promote immunosuppression and are a target in the field of immuno-oncology. Accumulation of MDSCs is associated with poor prognosis and resistance to immunotherapy for several cancers. Here, we describe an accumulation of a subset of circulating monocytic MDSCs (M-MDSC) overexpressing TIE2, the receptor for angiopoietin-2 (ANGPT2), in patients with non-small cell lung cancer (NSCLC). Greater numbers of circulating TIE2

Identifiants

pubmed: 31871121
pii: 2326-6066.CIR-19-0326
doi: 10.1158/2326-6066.CIR-19-0326
doi:

Substances chimiques

ANGPT2 protein, human 0
Angiopoietin-2 0
Biomarkers, Tumor 0
Receptor, TIE-2 EC 2.7.10.1
TEK protein, human EC 2.7.10.1

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

268-279

Informations de copyright

©2019 American Association for Cancer Research.

Auteurs

Elodie Lauret Marie Joseph (E)

Université Bourgogne Franche-Comté, INSERM, EFS, BFC, UMR1098, RIGHT, Besançon, France.

Caroline Laheurte (C)

Université Bourgogne Franche-Comté, INSERM, EFS, BFC, UMR1098, RIGHT, Besançon, France.
Etablissement Français du Sang Bourgogne Franche-Comté, Plateforme de Biomonitoring, Besançon, France.
INSERM CIC-1431, CHU Besançon, Besançon, France.

Marine Jary (M)

Université Bourgogne Franche-Comté, INSERM, EFS, BFC, UMR1098, RIGHT, Besançon, France.
Service d'Oncologie médicale, CHU Besançon, Besançon, France.

Laura Boullerot (L)

Université Bourgogne Franche-Comté, INSERM, EFS, BFC, UMR1098, RIGHT, Besançon, France.
INSERM CIC-1431, CHU Besançon, Besançon, France.

Kamal Asgarov (K)

Université Bourgogne Franche-Comté, INSERM, EFS, BFC, UMR1098, RIGHT, Besançon, France.

Eléonore Gravelin (E)

Université Bourgogne Franche-Comté, INSERM, EFS, BFC, UMR1098, RIGHT, Besançon, France.
INSERM CIC-1431, CHU Besançon, Besançon, France.

Adeline Bouard (A)

Université Bourgogne Franche-Comté, INSERM, EFS, BFC, UMR1098, RIGHT, Besançon, France.

Laurie Rangan (L)

Université Bourgogne Franche-Comté, INSERM, EFS, BFC, UMR1098, RIGHT, Besançon, France.

Magalie Dosset (M)

Université Bourgogne Franche-Comté, INSERM, EFS, BFC, UMR1098, RIGHT, Besançon, France.

Christophe Borg (C)

Université Bourgogne Franche-Comté, INSERM, EFS, BFC, UMR1098, RIGHT, Besançon, France.
INSERM CIC-1431, CHU Besançon, Besançon, France.
Service d'Oncologie médicale, CHU Besançon, Besançon, France.

Olivier Adotévi (O)

Université Bourgogne Franche-Comté, INSERM, EFS, BFC, UMR1098, RIGHT, Besançon, France. olivier.adotevi@univ-fcomte.fr.
Etablissement Français du Sang Bourgogne Franche-Comté, Plateforme de Biomonitoring, Besançon, France.
INSERM CIC-1431, CHU Besançon, Besançon, France.
Service d'Oncologie médicale, CHU Besançon, Besançon, France.

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Classifications MeSH