Abstract

Glioblastoma and other brain or CNS malignancies (like neuroblastoma and medulloblastoma) are difficult to treat and are characterized by excessive vascularization that favors further tumor growth. Since the mean overall survival of these types of diseases is low, the finding of new therapeutic approaches is imperative. In this review, we discuss the importance of the interaction between the endothelium and the tumor cells in brain and CNS malignancies. The different mechanisms of formation of new vessels that supply the tumor with nutrients are discussed. We also describe how the tumor cells (TC) alter the endothelial cell (EC) physiology in a way that favors tumorigenesis. In particular, mechanisms of EC–TC interaction are described such as (a) communication using secreted growth factors (i.e., VEGF, TGF-β), (b) intercellular communication through gap junctions (i.e., Cx43), and (c) indirect interaction via intermediate cell types (pericytes, astrocytes, neurons, and immune cells). At the signaling level, we outline the role of important mediators, like the gasotransmitter nitric oxide and different types of reactive oxygen species and the systems producing them. Finally, we briefly discuss the current antiangiogenic therapies used against brain and CNS tumors and the potential of new pharmacological interventions that target the EC–TC interaction.

Highlights

  • Malignant tumors of the central nervous system (CNS) are among the malignancies with the poorest prognosis

  • Based on these preclinical studies, a clinical phase I/II study was published in 2019, showing that the infusion of the CXCR4 inhibitor plerifaxor was well tolerated as an adjunct to standard chemoirradiation with newly diagnosed glioblastoma and improved local control of tumor recurrences [27]. The results from this clinical trial are encouraging; since this was a small and non-randomized study, future larger randomized trials are warranted. When it comes to pediatric tumors, it has been shown that high levels of circulating VEGF receptor 2 (VEGFR2)+ bone marrow-derived progenitor cells correlate with metastatic disease in children with solid malignancies, including brain tumors such as medulloblastoma, brain stem glioma, and brain stem pilocytic astrocytoma [28]

  • Vasculogenic mimicry (VM) is a phenomenon whereby the tumor cells themselves form “vessel-like structures” independent from angiogenesis based on endothelial cell (EC), generating a system that supplies the tumor with nutrients and oxygen [49]

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Summary

Brain and CNS Malignancies

Malignant tumors of the central nervous system (CNS) are among the malignancies with the poorest prognosis. This is indicated by the association of brain tumors with the highest estimated number of years (mean: ~20 years) of potential life lost due to any type of tumor [1]. We briefly describe the main types of brain and CNS malignancies such as gliomas, medulloblastomas, and neuroblastomas

Gliomas
Medulloblastomas
Neuroblastomas
Sprouting Angiogenesis
Intussusceptive Angiogenesis
Vasculogenic Mimicry and Transdifferentiation of Cancer Cells
Vascular Co-Option
Role of EMT and EndoMT in Brain Tumors
Levels of EC–Tumor Cell Interaction
Interaction with Secreted Factors
PDFG-B
Pleiotrophin
EVs and miRs
Direct Interaction via Gap Junctions
Pericytes
Astrocytes
Neurons
Findings
Conclusions and Future Prospects
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