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Cited by 337

The DOI matches its Crossref record; 5 of the 5 references it cites were found in a registry or an index.

Angiogenesis in malignant gliomas

Plate, Karl H., Risau, Werner·1995·Glia

Abstract

One event that accompanies glioma progression is the upregulation of angiogenesis. Low‐grade gliomas are moderately vascularized tumors whereas high‐grade gliomas show prominent microvascular proliferations and areas of high vascular density. To analyze the molecular mechanisms underlying glioma angiogenesis, we studied the expression of vascular endothelial growth factor (VEGF) and its tyrosine kinase receptors VEGFR‐1 and VEGFR‐2 during normal brain development and glioma‐induced angiogenesis. Our results suggest a paracrine control of angiogenesis and endothelial cell proliferation that is tightly regulated and transient in the embryonic brain, switched off in the normal adult brain, and turned on in tumor cells (VEGF) and the host vasculature (VEGFR‐1 and −2) during tumor progression. It is unknown how VEGF and VEGF receptors are upregulated during glioma angiogenesis, but there is recent evidence that VEGF as well as endogenous inhibitors of angiogenesis could be under control of the tumor suppressor genes p53 and VHL. © 1995 Wiley‐Liss, Inc.

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Metadata

Authors
Plate, K. H., & Risau, W.
Venue
Glia
Publisher
Wiley
Published
1995-11
Volume
15
Issue
3
Pages
339-347
ISSN
  • 0894-1491 (ISSN-L)
  • 1098-1136
OpenAlex
W1984284981
Cited by
337
References
5
FWCI
3.32
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Angiogenesis in malignant gliomas. https://app.cochat.ai/papers/10.1002/glia.440150313
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Plate, K. H., & Risau, W. (1995). Angiogenesis in malignant gliomas. Glia. https://doi.org/10.1002/glia.440150313

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