Intrinsic and Microenvironmental Drivers of Glioblastoma Invasion

Author:

De Fazio Emerson1,Pittarello Matilde2ORCID,Gans Alessandro3ORCID,Ghosh Bikona4ORCID,Slika Hasan5ORCID,Alimonti Paolo16,Tyler Betty5ORCID

Affiliation:

1. Department of Medicine, Vita-Salute San Raffaele University School of Medicine, 20132 Milan, Italy

2. Department of Medicine, Humanitas University School of Medicine, 20089 Rozzano, Italy

3. Department of Neurology, University of Milan, 20122 Milan, Italy

4. School of Medicine and Surgery, Dhaka Medical College, Dhaka 1000, Bangladesh

5. Hunterian Neurosurgical Laboratory, Department of Neurosurgery, Johns Hopkins University School of Medicine, Baltimore, MD 21231, USA

6. Department of Neurosurgery, Brigham and Women’s Hospital, Harvard Medical School, Boston, MA 02115, USA

Abstract

Gliomas are diffusely infiltrating brain tumors whose prognosis is strongly influenced by their extent of invasion into the surrounding brain tissue. While lower-grade gliomas present more circumscribed borders, high-grade gliomas are aggressive tumors with widespread brain infiltration and dissemination. Glioblastoma (GBM) is known for its high invasiveness and association with poor prognosis. Its low survival rate is due to the certainty of its recurrence, caused by microscopic brain infiltration which makes surgical eradication unattainable. New insights into GBM biology at the single-cell level have enabled the identification of mechanisms exploited by glioma cells for brain invasion. In this review, we explore the current understanding of several molecular pathways and mechanisms used by tumor cells to invade normal brain tissue. We address the intrinsic biological drivers of tumor cell invasion, by tackling how tumor cells interact with each other and with the tumor microenvironment (TME). We focus on the recently discovered neuronal niche in the TME, including local as well as distant neurons, contributing to glioma growth and invasion. We then address the mechanisms of invasion promoted by astrocytes and immune cells. Finally, we review the current literature on the therapeutic targeting of the molecular mechanisms of invasion.

Funder

Khatib Brain Tumor Center

Publisher

MDPI AG

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