Inhibition of guanosine monophosphate synthetase (GMPS) blocks glutamine metabolism and prostate cancer growth

J Pathol. 2021 Jun;254(2):135-146. doi: 10.1002/path.5665. Epub 2021 Apr 21.

Abstract

Glutamine is a critical nutrient in cancer; however, its contribution to purine metabolism in prostate cancer has not previously been determined. Guanosine monophosphate synthetase (GMPS) acts in the de novo purine biosynthesis pathway, utilizing a glutamine amide to synthesize the guanine nucleotide. This study demonstrates that GMPS mRNA expression correlates with Gleason score in prostate cancer samples, while high GMPS expression was associated with decreased rates of overall and disease/progression-free survival. Pharmacological inhibition or knockdown of GMPS significantly decreased cell growth in both LNCaP and PC-3 prostate cancer cells. We utilized [15 N-(amide)]glutamine and [U-13 C5 ]glutamine metabolomics to dissect the pathways involved and despite similar growth inhibition by GMPS knockdown, we show unique metabolic effects across each cell line. Using a PC-3 xenograft mouse model, tumor growth was also significantly decreased after GMPS knockdown, highlighting the importance of glutamine metabolism and providing support for GMPS as a therapeutic target in prostate cancer. © 2021 The Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.

Keywords: GMPS; cell growth; glutamine; immunohistochemistry; knockdown; metabolism; metabolomics; prostate cancer; purine; xenograft.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Carbon-Nitrogen Ligases / antagonists & inhibitors*
  • Carbon-Nitrogen Ligases / genetics
  • Carbon-Nitrogen Ligases / metabolism
  • Cell Line, Tumor
  • Cell Proliferation
  • Cohort Studies
  • Computational Biology
  • Disease Models, Animal
  • Gene Knockdown Techniques
  • Glutamine / metabolism*
  • Humans
  • Male
  • Metabolic Networks and Pathways
  • Metabolomics
  • Mice
  • Prostatectomy
  • Prostatic Neoplasms / enzymology*
  • Prostatic Neoplasms / pathology
  • Prostatic Neoplasms / surgery
  • Purines / metabolism
  • Tissue Array Analysis
  • Up-Regulation
  • Xenograft Model Antitumor Assays

Substances

  • Purines
  • Glutamine
  • Carbon-Nitrogen Ligases
  • GMP synthase (glutamine-hydrolyzing)
  • purine