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Expression of the endogenous galactose-binding protein galectin-3 correlates with the malignant potential of tumors in the central nervous system.

AbstractBACKGROUND:
The 31-kilodalton beta-galactoside-binding protein galectin-3 has been associated with cellular transformation and metastasis. Because neural tissues contain large amounts of glycoconjugates, and endogenous carbohydrate-binding proteins have been described in the human brain, the authors examined the expression of galectin-3 in human brain tumors and metastases to the central nervous system.
METHODS:
Brain tumors were categorized by the World Health Organization system and galectin-3 expression by immunoperoxidase staining using a quantitative staining score.
RESULTS:
Glioblastomas (Grade 4 astrocytomas) all stained strongly for galectin-3, whereas low grade astrocytomas (Grade 2) did not express the endogenous lectin. Anaplastic astrocytomas (Grade 3) exhibited intermediate expression. The staining score was significantly associated with tumor grade (P < 0.001). Normal brain tissue and benign tumors did not express galectin-3, whereas metastases to the brain were all positive for galectin-3 expression. Metastases expressed significantly more galectin-3 than the primary tumors from which they were derived (P = 0.003).
CONCLUSIONS:
Galectin-3 expression correlates with the malignant potential of tumors in the central nervous system.
AuthorsR S Bresalier, P S Yan, J C Byrd, R Lotan, A Raz
JournalCancer (Cancer) Vol. 80 Issue 4 Pg. 776-87 (Aug 15 1997) ISSN: 0008-543X [Print] United States
PMID9264362 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, P.H.S.)
Chemical References
  • Antigens, Differentiation
  • Galectin 3
  • Neoplasm Proteins
  • Galactose
Topics
  • Antigens, Differentiation (metabolism)
  • Astrocytoma (metabolism, pathology)
  • Brain Neoplasms (metabolism, pathology, secondary)
  • Galactose (metabolism)
  • Galectin 3
  • Glioblastoma (metabolism, pathology)
  • Humans
  • Immunohistochemistry
  • Neoplasm Proteins (metabolism)
  • Protein Binding

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