Peritoneal colonization by human pancreatic cancer cells is inhibited by antisense FUT3 sequence

Int J Cancer. 2000 Nov 15;88(4):558-65. doi: 10.1002/1097-0215(20001115)88:4<558::aid-ijc7>3.0.co;2-b.

Abstract

Several alpha(1,3/1,4) fucosyltransferases expressed in human pancreatic cancer cells can participate in the biosynthesis of cell surface sialyl-Lewis a and sialyl-Lewis x antigens that contribute to hematogenous metastatis. Previously, we observed a significant increase of the alpha(1,4) fucosyltransferase activity in tumoral pancreatic cell lines, suggesting that FUT3 could be involved in the sialyl-Lewis antigen expression. Therefore, we invalidated the expression of FUT3 by expressing FUT3 antisense sequence in the human pancreatic tumor BxPC-3 cell line, which expresses the alpha(1,4) fucosyltransferase activity and harbors the cell surface sialyl-Lewis antigens. The decrease of FUT3 transcript after transfection of antisense cDNA of FUT3 in these cells results in a substantial reduction of sialyl-Lewis antigen expression on cell surface. This decreased antigen expression was associated with an inhibition of adhesive properties to E-selectin and a decrease of metastatic power of FUT3 antisense-transfected BxPC-3 cells as tested in nude mice. Our study provides evidence that the expression level of FUT3 may regulate the expression of sialyl-Lewis a and sialyl-Lewis x surface antigens and consequently could play an important role in metastatic properties of human pancreatic cancer cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • CHO Cells
  • Cricetinae
  • E-Selectin / genetics
  • E-Selectin / physiology
  • Female
  • Fucosyltransferases / genetics*
  • Fucosyltransferases / metabolism
  • Humans
  • Mice
  • Mice, Nude
  • Oligosaccharides / analysis
  • Pancreatic Neoplasms / enzymology
  • Pancreatic Neoplasms / genetics
  • Pancreatic Neoplasms / pathology*
  • Peritoneal Neoplasms / genetics
  • Peritoneal Neoplasms / pathology
  • Peritoneal Neoplasms / prevention & control
  • Peritoneal Neoplasms / secondary*
  • RNA, Antisense / genetics*
  • RNA, Messenger / genetics
  • Reverse Transcriptase Polymerase Chain Reaction
  • Sialyl Lewis X Antigen
  • Transcription, Genetic
  • Tumor Cells, Cultured
  • Xenograft Model Antitumor Assays

Substances

  • E-Selectin
  • Oligosaccharides
  • RNA, Antisense
  • RNA, Messenger
  • Sialyl Lewis X Antigen
  • Fucosyltransferases
  • 3-galactosyl-N-acetylglucosaminide 4-alpha-L-fucosyltransferase