Friends with Benefits: Chemokines, Glioblastoma-Associated Microglia/Macrophages, and Tumor Microenvironment.

chemokine dendritic cells gene editing glioblastoma glioblastoma-associated macrophages glioblastoma-associated microglia myeloid-derived suppressor cells soluble factors specific receptors tumor infiltrating lymphocytes tumor microenvironment

Journal

International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791

Informations de publication

Date de publication:
24 Feb 2022
Historique:
received: 27 01 2022
revised: 17 02 2022
accepted: 22 02 2022
entrez: 10 3 2022
pubmed: 11 3 2022
medline: 9 4 2022
Statut: epublish

Résumé

Glioma is the most common primary intracranial tumor and has the greatest prevalence of all brain tumors. Treatment resistance and tumor recurrence in GBM are mostly explained by considerable alterations within the tumor microenvironment, as well as extraordinary cellular and molecular heterogeneity. Soluble factors, extracellular matrix components, tissue-resident cell types, resident or newly recruited immune cells together make up the GBM microenvironment. Regardless of many immune cells, a profound state of tumor immunosuppression is supported and developed, posing a considerable hurdle to cancer cells' immune-mediated destruction. Several studies have suggested that various GBM subtypes present different modifications in their microenvironment, although the importance of the microenvironment in treatment response has yet to be determined. Understanding the microenvironment and how it changes after therapies is critical because it can influence the remaining invasive GSCs and lead to recurrence. This review article sheds light on the various components of the GBM microenvironment and their roles in tumoral development, as well as immune-related biological processes that support the interconnection/interrelationship between different cell types. Also, we summarize the current understanding of the modulation of soluble factors and highlight the dysregulated inflammatory chemokine/specific receptors cascades/networks and their significance in tumorigenesis, cancer-related inflammation, and metastasis.

Identifiants

pubmed: 35269652
pii: ijms23052509
doi: 10.3390/ijms23052509
pmc: PMC8910233
pii:
doi:

Substances chimiques

Chemokines 0
Receptors, Chemokine 0

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Ministerul Cercetării și Inovării
ID : PNIII.P2-2.1-PED-2019-3141, PN 19.29.01.04, ID: P_40_197/2016, 31PFE/30.12.2021

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Front Immunol. 2018 Nov 27;9:2750
pubmed: 30542347

Auteurs

Elena Codrici (E)

Victor Babes National Institute of Pathology, 050096 Bucharest, Romania.

Ionela-Daniela Popescu (ID)

Victor Babes National Institute of Pathology, 050096 Bucharest, Romania.

Cristiana Tanase (C)

Victor Babes National Institute of Pathology, 050096 Bucharest, Romania.
Department of Clinical Biochemistry, Faculty of Medicine, Titu Maiorescu University, 031593 Bucharest, Romania.

Ana-Maria Enciu (AM)

Victor Babes National Institute of Pathology, 050096 Bucharest, Romania.
Department of Cell Biology and Histology, Carol Davila University of Medicine and Pharmacy, 050474 Bucharest, Romania.

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