Toll-like Receptor-4 Activation Boosts the Immunosuppressive Properties of Tumor Cells-derived Exosomes.


Journal

Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288

Informations de publication

Date de publication:
11 06 2019
Historique:
received: 22 10 2018
accepted: 24 05 2019
entrez: 13 6 2019
pubmed: 13 6 2019
medline: 21 10 2020
Statut: epublish

Résumé

The biology of tumor-derived exosomes (TEX) is only partially understood and much remains to be studied in order to define the effect that the tumor microenvironment or the activation of tumor cells exerts on their composition and functions. Increased expression and activity of toll-like receptor 4 (TLR4) in chronic infectious and inflammatory conditions is related with cancer progression: its activation induces an inflammatory signaling that increases the tumorigenic potential of cancer cells promoting their immune evasion. We investigated the immune modulatory properties of TEX released upon cell TLR4 activation, and we found that, although differences were observed depending on the type of the tumor, the treatment influences TEX composition and boosts their immunosuppressive ability. Our results suggest that the activation of TLR4 supports tumor progression by stimulating the release of more effective immunosuppressive exosomes, which allow tumor cells to escape immune surveillance and probably even play a role in the metastatic process.

Identifiants

pubmed: 31186484
doi: 10.1038/s41598-019-44949-y
pii: 10.1038/s41598-019-44949-y
pmc: PMC6560033
doi:

Substances chimiques

Immunosuppressive Agents 0
MicroRNAs 0
TLR4 protein, human 0
Toll-Like Receptor 4 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

8457

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Auteurs

Rossana Domenis (R)

Dipartimento di Area Medica (DAME), Università degli Studi di Udine, Udine, Italy.

Adriana Cifù (A)

Dipartimento di Area Medica (DAME), Università degli Studi di Udine, Udine, Italy.

Daniele Marinò (D)

Dipartimento di Area Medica (DAME), Università degli Studi di Udine, Udine, Italy.

Martina Fabris (M)

Dipartimento di Area Medica (DAME), Università degli Studi di Udine, Udine, Italy.
Istituto di Patologia Clinica, Azienda Sanitaria Universitaria Integrata di Udine (ASUID), Udine, Italy.

Kayvan R Niazi (KR)

NantBioScience, Inc Culver City, CA, 90232, USA.

Patrick Soon-Shiong (P)

NantBioScience, Inc Culver City, CA, 90232, USA.

Francesco Curcio (F)

Dipartimento di Area Medica (DAME), Università degli Studi di Udine, Udine, Italy. francesco.curcio@uniud.it.
Istituto di Patologia Clinica, Azienda Sanitaria Universitaria Integrata di Udine (ASUID), Udine, Italy. francesco.curcio@uniud.it.

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Classifications MeSH