Transcript quantification of Dresden G protein-coupled receptor (D-GPCR) in primary prostate cancer tissue pairs

Research output: Contribution to journalResearch articleContributedpeer-review

Contributors

  • Susanne Fuessel - , Department of Urology (Author)
  • Bernd Weigle - , TUD Dresden University of Technology (Author)
  • Uta Schmidt - , TUD Dresden University of Technology (Author)
  • Gustavo Baretton - , Institute of Pathology (Author)
  • Rainer Koch - , TUD Dresden University of Technology (Author)
  • Michael Bachmann - , Institute for Immunology (Author)
  • E. Peter Rieber - , TUD Dresden University of Technology (Author)
  • Manfred P. Wirth - , TUD Dresden University of Technology (Author)
  • Axel Meye - , TUD Dresden University of Technology (Author)

Abstract

Recently, we identified the novel protein D-GPCR (Dresden G protein-coupled receptor) which is selectively overexpressed in human prostate cancer (PCa) and belongs to the subfamily of odorant-like orphan GPCRs. Quantification of D-GPCR transcripts in paired malignant and non-malignant prostate tissues of 106 patients with primary PCa by real-time PCR demonstrated a significant up-regulation of this gene in tumor samples. Furthermore, its expression increases with higher tumor stages and grades. The evaluation of D-GPCR expression as a potential molecular tumor marker was performed by receiver-operating characteristic curve (ROC) analysis resulting in an area under the curve (AUC) value of 0.6452. Hence, the evaluation of D-GPCR as possible additive diagnostic tool and putative therapy target appears promising.

Details

Original languageEnglish
Pages (from-to)95-104
Number of pages10
JournalCancer letters
Volume236
Issue number1
Publication statusPublished - 8 May 2006
Peer-reviewedYes

External IDs

PubMed 15979782

Keywords

Sustainable Development Goals

ASJC Scopus subject areas

Keywords

  • Expression profile, G protein-coupled receptor, LightCycler, Prostate cancer, Quantitative real-time PCR