Mechanisms of cancer-associated glycosylation changes

Front Biosci (Landmark Ed). 2012 Jan 1;17(2):670-99. doi: 10.2741/3951.

Abstract

Cell membrane glycoconjugates undergo characteristic changes as a consequence of neoplastic transformation. The cancer-associated carbohydrate structures play key roles in cancer progression by altering the cell-cell and cell-environment interactions. In this review, we will discuss some of the most relevant cancer-associated carbohydrate structures, including the β1,6-branching of N-linked chains, the sialyl Lewis antigens, the α2,6-sialylated lactosamine, the Thomsen-Friedenreich-related antigens and gangliosides. We will describe the mechanisms leading to the expression of these structures and their interactions with sugar binding molecules, such as selectins and galectins. Finally, we will discuss how the glycosylation machinery of the cell is controlled by signal transduction pathways, epigenetic mechanisms and responds to hypoxia.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Antigens, Tumor-Associated, Carbohydrate / chemistry
  • Antigens, Tumor-Associated, Carbohydrate / metabolism
  • Carbohydrate Metabolism
  • Carbohydrate Sequence
  • Cell Membrane / metabolism
  • Cell Transformation, Neoplastic
  • Epigenesis, Genetic
  • Genes, Tumor Suppressor
  • Glycoconjugates / chemistry
  • Glycoconjugates / genetics
  • Glycoconjugates / metabolism*
  • Glycosylation
  • Humans
  • Hypoxia / genetics
  • Hypoxia / metabolism
  • Molecular Sequence Data
  • Neoplasms / genetics
  • Neoplasms / metabolism*
  • Oncogenes

Substances

  • Antigens, Tumor-Associated, Carbohydrate
  • Glycoconjugates