Development of alkyl glycerone phosphate synthase inhibitors: Structure-activity relationship and effects on ether lipids and epithelial-mesenchymal transition in cancer cells

Eur J Med Chem. 2019 Feb 1:163:722-735. doi: 10.1016/j.ejmech.2018.11.050. Epub 2018 Nov 28.

Abstract

In aggressive tumors, alkylglyceronephosphate synthase (AGPS) controls cellular ether phospholipid utilization and metabolism to promote cancer cell proliferation and motility. SAR studies on the first-in-class AGPS inhibitor 1, discovered by our group, led to the 2,6-difluoro analog 2i which showed higher binding affinity than 1in vitro. In 231MFP cancer cells, 2i reduced ether lipids levels and cell migration rate. When tested in PC-3 and MDA-MB-231 cancer cells, 2i specifically impaired epithelial to mesenchymal transition (EMT) by modulating E-cadherin, Snail and MMP2 expression levels. Moreover, the combination of siRNAs against AGPS and 2i provided no additive effect, confirming that the modulation of 2i on EMT specifically relies on AGPS inhibition. Finally, this compound also affected cancer cell proliferation especially in MDA-MB-231 cells expressing higher AGPS level, whereas it provided negligible effects on MeT5A, a non-tumorigenic cell line, thus showing cancer specificity.

Keywords: AGPS inhibitors; Cancer; E-cadherin; Ether lipids; Snail.

MeSH terms

  • Alkyl and Aryl Transferases / antagonists & inhibitors*
  • Cadherins / metabolism
  • Cell Line
  • Cell Line, Tumor
  • Cell Movement / drug effects
  • Cell Proliferation / drug effects
  • Epithelial-Mesenchymal Transition / drug effects*
  • Humans
  • Lipid Metabolism / drug effects*
  • Matrix Metalloproteinase 2 / metabolism
  • Neoplasms / drug therapy
  • Neoplasms / pathology*
  • Snail Family Transcription Factors / metabolism
  • Structure-Activity Relationship

Substances

  • Cadherins
  • Snail Family Transcription Factors
  • Alkyl and Aryl Transferases
  • alkylglycerone-phosphate synthase
  • MMP2 protein, human
  • Matrix Metalloproteinase 2