4.8 Article

Transition of Mesenchymal and Epithelial Cancer Cells Depends on alpha 1-4 Galactosyltransferase-Mediated Glycosphingolipids

Journal

CANCER RESEARCH
Volume 78, Issue 11, Pages 2952-2965

Publisher

AMER ASSOC CANCER RESEARCH
DOI: 10.1158/0008-5472.CAN-17-2223

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Funding

  1. Swiss National Foundation [310030-156982, 310030_143619, 32, Sinergia 171037]
  2. Krebsliga Schweiz [KFS_3013-08-2012, KIES-3841-02-2016]
  3. Krebsliga beider Basel [06-2013]
  4. Novartis Foundation for Biomedical Research [138093]
  5. Novartis
  6. Department of Biomedicine, university Hospital Basel
  7. University of Basel
  8. Australian Research Council Centre of Excellence in Nanoscale Biophotonics [CE140100003]

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The reversible transitions of cancer cells between epithelial and mesenchymal states comprise cellular and molecular processes essential for local tumor growth and respective dissemination. We report here that globoside glycosphingolipid (GSL) glycosyltransferase-encoding genes are elevated in epithelial cells and correlate with characteristic EMT signatures predictive of disease outcome. Depletion of globosides through CRISPR-Cas9-mediated deletion of the key enzyme A4GALT induces EMT, enhances chemoresistance, and increased CD24(low)/CD44(high) cells. The cholera toxin-induced mesenchymal-to-epithelial transition occurred only in cells with functional A4GALT. Cells undergoing EMT lost E-cadherin expression through epigenetic silencing at the promoter region of CDH1. However, in Delta A4GALT cells, demethylation was able to rescue E-cadherin-mediated cell-cell adhesion only in the presence of exogenous A4GALT. Overall, our data suggest another class of biomolecules vital for epithelial cancer cells and for maintaining cell integrity and function. Significance: This study highlights the essential role of glycosphingolipids in the maintenance of epithelial cancer cell properties. (C) 2018 AACR.

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