Glioblastoma Tumor Microenvironment: An Important Modulator for Tumoral Progression and Therapy Resistance

Author:

Tataranu Ligia Gabriela12ORCID,Turliuc Serban3ORCID,Kamel Amira2ORCID,Rizea Radu Eugen12ORCID,Dricu Anica4ORCID,Staicu Georgiana-Adeline4ORCID,Baloi Stefania Carina4ORCID,Rodriguez Silvia Mara Baez2,Manole Andrada Ioana Maria2

Affiliation:

1. Neurosurgical Department, University of Medicine and Pharmacy “Carol Davila”, 020022 Bucharest, Romania

2. Neurosurgical Department, Clinical Emergency Hospital “Bagdasar-Arseni”, 041915 Bucharest, Romania

3. Medical Department, University of Medicine and Pharmacy “G. T. Popa”, 700115 Iasi, Romania

4. Biochemistry Department, University of Medicine and Pharmacy, 200349 Craiova, Romania

Abstract

The race to find an effective treatment for glioblastoma (GBM) remains a critical topic, because of its high aggressivity and impact on survival and the quality of life. Currently, due to GBM’s high heterogeneity, the conventional treatment success rate and response to therapy are relatively low, with a median survival rate of less than 20 months. A new point of view can be provided by the comprehension of the tumor microenvironment (TME) in pursuance of the development of new therapeutic strategies to aim for a longer survival rate with an improved quality of life and longer disease-free interval (DFI). The main components of the GBM TME are represented by the extracellular matrix (ECM), glioma cells and glioma stem cells (GSCs), immune cells (microglia, macrophages, neutrophils, lymphocytes), neuronal cells, all of them having dynamic interactions and being able to influence the tumoral growth, progression, and drug resistance thus being a potential therapeutic target. This paper will review the latest research on the GBM TME and the potential therapeutic targets to form an up-to-date strategy.

Publisher

MDPI AG

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