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

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.
AuthorsGiulia Stazi, Cecilia Battistelli, Valentina Piano, Roberta Mazzone, Biagina Marrocco, Sara Marchese, Sharon M Louie, Clemens Zwergel, Lorenzo Antonini, Alexandros Patsilinakos, Rino Ragno, Monica Viviano, Gianluca Sbardella, Alessia Ciogli, Giancarlo Fabrizi, Roberto Cirilli, Raffaele Strippoli, Alessandra Marchetti, Marco Tripodi, Daniel K Nomura, Andrea Mattevi, Antonello Mai, Sergio Valente
JournalEuropean journal of medicinal chemistry (Eur J Med Chem) Vol. 163 Pg. 722-735 (Feb 01 2019) ISSN: 1768-3254 [Electronic] France
PMID30576903 (Publication Type: Journal Article)
CopyrightCopyright © 2018 Elsevier Masson SAS. All rights reserved.
Chemical References
  • Cadherins
  • Snail Family Transcription Factors
  • Alkyl and Aryl Transferases
  • alkylglycerone-phosphate synthase
  • MMP2 protein, human
  • Matrix Metalloproteinase 2
Topics
  • 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, pathology)
  • Snail Family Transcription Factors (metabolism)
  • Structure-Activity Relationship

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