Tumor vasculature and glioma stem cells: Contributions to glioma progression
•Glioma-derived endothelial cells (EC) are functionally distinct from normal brain EC.•The tumor vasculature can regulate glioma stem cell self-renewal and tumorigenicity.•Glioma stem cells contribute to tumor angiogenesis. Glioblastoma multiforme (GBM), the most malignant of brain tumors, is charac...
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Published in | Cancer letters Vol. 380; no. 2; pp. 545 - 551 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
Ireland
Elsevier B.V
01.10.2016
Elsevier Limited |
Subjects | |
Online Access | Get full text |
ISSN | 0304-3835 1872-7980 1872-7980 |
DOI | 10.1016/j.canlet.2014.12.028 |
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Summary: | •Glioma-derived endothelial cells (EC) are functionally distinct from normal brain EC.•The tumor vasculature can regulate glioma stem cell self-renewal and tumorigenicity.•Glioma stem cells contribute to tumor angiogenesis.
Glioblastoma multiforme (GBM), the most malignant of brain tumors, is characterized by extensive vascularization and a high degree of invasion. The current standard of care is not very effective, resulting in tumor recurrence with patients rarely surviving over 2 years. This tumor recurrence is attributed to the presence of chemo and radiation resistant glioma stem cells (GSCs). These cells are associated with vascular niches which regulate GSC self-renewal and survival. Recent studies suggest that while blood vessels support glioma stem cells, these tumor cells in turn may regulate and contribute to the tumor vasculature by transdifferentiating into endothelial cells directly or through the secretion of regulatory growth factors such as vascular endothelial growth factor (VEGF) and hepatoma derived growth factor (HDGF). The relationship between the tumor vasculature and the glioma stem cells is the subject of this review. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 ObjectType-Review-3 content type line 23 |
ISSN: | 0304-3835 1872-7980 1872-7980 |
DOI: | 10.1016/j.canlet.2014.12.028 |