Abstract
Mechanisms responsible for the progression of malignant melanoma to highly aggressive brain-metastatic disease remain largely unknown. Brain neurotrophins can modulate the brain invasion of melanoma cells and the activity of an enzyme called heparanase. Heparanase is an endo-β-glucuronidase that degrades the heparan sulfate chains of heparan sulfate proteoglycans, essential and ubiquitous macromolecules associated with the cell surface and the extracellular matrix of a wide range of cells and tissues. Human heparanase has been recently cloned as a single gene family and found to be a potential target for anticancer drugs because of its critical roles in anglogenic and invasive processes. The potential relevance of heparanase, as a cellular switch from noninvasive to the invasive phenotype and novel therapeutic target for invasive brain tumors, is introduced.
Original language | English (US) |
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Pages (from-to) | 459-463 |
Number of pages | 5 |
Journal | Expert Review of Neurotherapeutics |
Volume | 2 |
Issue number | 4 |
DOIs | |
State | Published - 2002 |
Keywords
- Astrocytes
- Brain invasion and angiogenesis
- Brain metastasis
- Extracellular matrix degradation
- Heparanase
- Neurotrophins
ASJC Scopus subject areas
- General Neuroscience
- Clinical Neurology
- Pharmacology (medical)