Targeting Tumor Associated Macrophages to Overcome Conventional Treatment Resistance in Glioblastoma.

crosstalks glioblastoma macrophages microglia radiation resistance tumor-associated macrophage

Journal

Frontiers in pharmacology
ISSN: 1663-9812
Titre abrégé: Front Pharmacol
Pays: Switzerland
ID NLM: 101548923

Informations de publication

Date de publication:
2020
Historique:
received: 23 12 2019
accepted: 10 03 2020
entrez: 24 4 2020
pubmed: 24 4 2020
medline: 24 4 2020
Statut: epublish

Résumé

Glioblastoma (GB) is the most common and devastating form of brain cancer. Despite conventional treatments, progression or recurrences are systematic. In recent years, immunotherapies have emerged as an effective treatment in a number of cancers, leaving the question of their usefulness also faced with the particular case of brain tumors. The challenge here is major not only because the brain is the seat of our consciousness but also because of its isolation by the blood-brain barrier and the presence of a unique microenvironment that constitutes the central nervous system (CNS) with very specific constituent or patrolling cells. Much of the microenvironment is made up of immune cells or inflammation. Among these, tumor-associated macrophages (TAMs) are of significant interest as they are often involved in facilitating tumor progression as well as the development of resistance to standard therapies. In this review, the ubiquity of TAMs in GB will be discussed while the specific case of microglia resident in the brain will be also emphasized. In addition, the roles of TAMs as accomplices in the progression of GB and resistance to treatment will be presented. Finally, clinical trials targeting TAMs as a means of treating cancer will be discussed.

Identifiants

pubmed: 32322199
doi: 10.3389/fphar.2020.00368
pmc: PMC7158850
doi:

Types de publication

Journal Article Review

Langues

eng

Pagination

368

Informations de copyright

Copyright © 2020 Grégoire, Roncali, Rousseau, Chérel, Delneste, Jeannin, Hindré and Garcion.

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Auteurs

Hélène Grégoire (H)

CRCINA, INSERM, Université de Nantes, Université d'Angers, Angers, France.

Loris Roncali (L)

CRCINA, INSERM, Université de Nantes, Université d'Angers, Angers, France.

Audrey Rousseau (A)

CRCINA, INSERM, Université de Nantes, Université d'Angers, Angers, France.
Département de Pathologie Cellulaire et Tissulaire, CHU Angers, Angers, France.

Michel Chérel (M)

CRCINA, INSERM, Université d'Angers, Université de Nantes, Nantes, France.

Yves Delneste (Y)

CRCINA, INSERM, Université de Nantes, Université d'Angers, Angers, France.
Laboratoire d'Immunologie et Allergologie, CHU d'Angers, Angers, France.

Pascale Jeannin (P)

CRCINA, INSERM, Université de Nantes, Université d'Angers, Angers, France.
Laboratoire d'Immunologie et Allergologie, CHU d'Angers, Angers, France.

François Hindré (F)

CRCINA, INSERM, Université de Nantes, Université d'Angers, Angers, France.
PRIMEX, Plateforme de radiobiologie et d'imagerie expérimentale, SFR ICAT, Université d'Angers, Angers, France.

Emmanuel Garcion (E)

CRCINA, INSERM, Université de Nantes, Université d'Angers, Angers, France.
PACeM, Plateforme d'analyses cellulaires et moléculaires, SFR ICAT, Université d'Angers, Angers, France.

Classifications MeSH