ACTA FAC MED NAISS 2020;37(3):211-230 |
Review article
UDC:
616.831-006.48:612
DOI:
10.5937/afmnai2003211T
Angiogenesis in Glioblastoma: Molecular and Cellular Mechanisms and Clinical
Applications
Desanka Tasić2,4, Irena Dimov5,
Miloš Kostov6, Nataša Vidović3, Dragan Dimov2,4
1University of Niš, Faculty of Medicine,
Niš, Serbia
2University of Niš, Faculty of Medicine,
Retired professor, Niš, Serbia
4Center for Pathology and Pathological
Anatomy, Retired pathologist, Niš, Serbia
SUMMARY
Glioblastoma (GBM) is the most
common malignant primary brain tumor in adults and carries
poor prognosis. Despite advances in therapy, no significant increase in
survival has been achieved for GBM patients. These tumors inevitably recur in
the majority of patients, and the therapeutic options for recurrent tumors are
limited. GBMs are aggressive, fast-growing, and highly infiltrative tumors, with
exuberant angiogenesis (microvascular proliferation) and necrosis. However, the
newly formed tumor vessels are structurally and functionally abnormal, creating
areas of hypoxia and ultimately necrosis, contributing to tumor progression and
aggressiveness. Since GBMs are hypervascular in nature, targeting tumor
angiogenesis emerged as a promising therapeutic strategy.
In this review, we summarized
the molecular and cellular mechanisms governing GBM angiogenesis, the other
modes of tumor vascularization, and the key mediators of these processes. We
also discussed the importance of tumor hypoxia in promoting angiogenic and
vasculogenic processes, the contributions of GBM stem cells to tumor
vasculature, the anti-angiogenic therapy for GBM, and the resistance to such
therapy. A better understanding of the molecular and cellular basis of GBM
neovascularization, the mechanisms of resistance to therapy, and the
contributions of GBM stem cells to tumor vasculature will lead to the
development of more effective treatment strategies.
Key words:
glioblastoma (GBM), angiogenesis, vasculogenesis, hypoxia, GBM stem cells, anti-angiogenic
therapy, resistance