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Elevated expression of H type GDP-L-fucose:β-D-galactoside α-2-L-fucosyltransferase is associated with human colon adenocarcinoma progression

  • Jing Sun
  • , Jan Thurin
  • , Harry S. Cooper
  • , Ping Wang
  • , Miroslaw Mackiewicz
  • , Zenon Steplewski
  • , Magdalena Blaszczyk-Thurin
  • Wistar Institute
  • Hahnemann University

Research output: Contribution to journalArticlepeer-review

60 Scopus citations

Abstract

GDP-L-fucose:β-D-galactoside α-2-L-fucosyltransferase (EC 2.4.1.69) is a key enzyme in the biosynthesis of fucosylated type 1 and 2 lactoseries structures, such as Lewis b and the H type 2 and Lewis Y, respectively, that are accumulated in colon adenocarcinoma. Analysis of the mRNA transcript level for the human H gene-encoded β-D-galactoside α-2-L-fucosyltransferase revealed 40- and 340-fold increases in the mRNA levels in all adenocarcinomas and tumor cell lines, respectively, compared to normal colon mucosa where a low level of mRNA transcript was detected. A variable increase in mRNA transcript levels was observed in 50% of adenomatous polyps. Nucleotide sequence analysis of the protein coding region of the cDNAs derived from normal colon, adenoma, and colon adenocarcinoma revealed 100% homology, suggesting that there are no tumor-associated allelic variations within the H β-D-galactoside α-2-L-fucosyltransferase cDNA. These results suggest that β-D-galactoside α-2-L-fucosyltransferase expression highly correlates with malignant progression of colon adenocarcinoma.

Original languageEnglish
Pages (from-to)5724-5728
Number of pages5
JournalProceedings of the National Academy of Sciences of the United States of America
Volume92
Issue number12
DOIs
StatePublished - Jun 6 1995

Keywords

  • Adenocarcinoma/enzymology
  • Animals
  • Base Sequence
  • Carbohydrates/immunology
  • Cloning, Molecular
  • Colonic Neoplasms/enzymology
  • DNA Primers
  • DNA, Complementary
  • Disease Progression
  • Epitopes/analysis
  • Fucosyltransferases/genetics
  • Galactoside 2-alpha-L-fucosyltransferase
  • Humans
  • Molecular Sequence Data
  • Polymerase Chain Reaction
  • RNA, Messenger/genetics
  • Transfection
  • Tumor Cells, Cultured

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