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Article
Effects of global O-GlcNAcylation on galectin gene-expression profiles in human cancer cell lines
Anticancer Research
  • Ali A. Sherazi, Western University
  • Komal A. Jariwala, Western University
  • Amanda N. Cybulski, Western University
  • Justin W. Lewis, Western University
  • Jim Karagiannis, Western University
  • Robert C. Cumming, Western University
  • Alexander V. Timoshenko, Western University
Document Type
Article
Publication Date
12-1-2018
URL with Digital Object Identifier
10.21873/anticanres.13037
Abstract

Background/Aim: The effects of O-linked β-N-acetyl-D-glucosamine (O-GlcNAc) transferase (OGT) and O-GlcNAcase (OGA) inhibitors on galectin gene expression profiles were examined in MCF7, HT-29, and HL-60 cancer cell lines. Materials and Methods: Cell cultures were treated for 24 h with OGA inhibitor thiamet G or OGT inhibitor 2-acetamido-1,3,4,6-tetra-O-acetyl-2-deoxy-5-thio-α-D-glucopyranose, and global O-GlcNAc levels and expression of galectin genes were determined using an immunodot blot assay and real-time quantitative polymerase chain reaction. Results: Two galectin genes, LGALS3 in MCF7 cells and LGALS12 in HL-60 cells, were up-regulated by O-GlcNAc, whereas other cell-specific galectins were unresponsive to changes in O-GlcNAc level. Of interest, basal levels of O-GlcNAc in resting HL-60 and HT-29 cells were significantly higher than those in cells differentiated into neutrophilic or enterocytic lineages, respectively. Conclusion: O-GlcNAc-mediated signaling pathways may be involved in regulating the expression of only a limited number of galectin genes. Additional O-GlcNAc-dependent mechanisms may work at the protein level (galectin secretion and intracellular localization) and warrant further investigation.

Citation Information
Ali A. Sherazi, Komal A. Jariwala, Amanda N. Cybulski, Justin W. Lewis, et al.. "Effects of global O-GlcNAcylation on galectin gene-expression profiles in human cancer cell lines" Anticancer Research Vol. 38 Iss. 12 (2018) p. 6691 - 6697
Available at: http://works.bepress.com/robert-cumming/4/