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Metastasis of human colon cancer is altered by modifying expression of the beta-galactoside-binding protein galectin 3.

AbstractBACKGROUND & AIMS:
Galectin 3 is a beta-galactoside-binding protein whose expression has been correlated with advanced tumor stage in the colon, but direct evidence for a role in metastasis is lacking. The current study was designed to more directly establish the role of galectin 3 in colon cancer metastasis.
METHODS:
Galectin 3 levels were manipulated in human colon cancer cells using eukaryotic expression constructs designed to express the complete galectin 3 complementary DNA in either the sense or antisense orientation. Liver colonization was assessed in athymic mice after splenic-portal inoculation or after spontaneous metastasis during cecal growth.
RESULTS:
Introduction of galectin 3 antisense into metastatic colon cancer cells (LSLiM6, HM7) resulted in a significant reduction in galectin 3-specific messenger RNA and total and cell surface galectin 3 protein. Conversely, stable integration of galectin 3 in the sense orientation resulted in an increase in cellular and cell surface galectin 3 in cells of low metastatic potential (LS174T). Reduction in galectin 3 levels was associated with a marked decrease in liver colonization and spontaneous metastasis by LSLiM6 and HM7 cells, whereas up-regulation of galectin 3 resulted in increased metastasis by LS174T cells.
CONCLUSIONS:
This study provides direct evidence that galectin 3 plays an important role in colon cancer metastasis.
AuthorsR S Bresalier, N Mazurek, L R Sternberg, J C Byrd, C K Yunker, P Nangia-Makker, A Raz
JournalGastroenterology (Gastroenterology) Vol. 115 Issue 2 Pg. 287-96 (Aug 1998) ISSN: 0016-5085 [Print] United States
PMID9679034 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, P.H.S.)
Chemical References
  • Antigens, Differentiation
  • Antisense Elements (Genetics)
  • Galactosides
  • Galectin 3
  • beta-galactoside
Topics
  • Adenocarcinoma (metabolism, secondary)
  • Animals
  • Antigens, Differentiation (metabolism)
  • Antisense Elements (Genetics) (genetics)
  • Cell Line, Transformed
  • Cell Membrane (metabolism)
  • Colonic Neoplasms (metabolism, pathology)
  • Galactosides (metabolism)
  • Galectin 3
  • Humans
  • Mice
  • Mice, Nude
  • Tissue Distribution
  • Transfection (genetics)
  • Tumor Cells, Cultured

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