Prognostic relevance of uPAR-del4/5 and TIMP-3 mRNA expression levels in breast cancer

Research output: Contribution to journalResearch articleContributedpeer-review

Contributors

  • Matthias Kotzsch - , Institute of Pathology (Author)
  • Juliane Farthmann - , Technical University of Munich (Author)
  • Axel Meye - , Department of Urology (Author)
  • Susanne Fuessel - , Department of Urology (Author)
  • Gustavo Baretton - , Institute of Pathology (Author)
  • Vivianne C.G. Tjan-Heijnen - , Radboud University Nijmegen (Author)
  • Manfred Schmitt - , Technical University of Munich (Author)
  • Thomas Luther - , Medical Laboratory East Saxony , Institute of Pathology (Author)
  • Fred C.G.J. Sweep - , Radboud University Nijmegen (Author)
  • Viktor Magdolen - , Technical University of Munich (Author)
  • Paul N. Span - , Radboud University Nijmegen (Author)

Abstract

Recently, two components of important protease systems in cancer, i.e., the urokinase plasminogen activator receptor (uPAR) mRNA splice variant uPAR-del4/5 and the tissue inhibitor of matrix metalloproteinase-3 (TIMP-3), were independently reported to be of prognostic value in breast cancer. In the present study, we have evaluated the impact of both these factors on disease-free survival (DFS) in 205 breast cancer patients by assessing mRNA expression in tumour tissue by quantitative PCR. High uPAR-del4/5 mRNA expression was associated with shorter DFS in breast cancer patients (P = 0.0363), whereas high TIMP-3 mRNA levels were associated with a good prognosis (P = 0.0049). Furthermore, by combining uPAR-del4/5 with TIMP-3 values, we demonstrate that breast cancer patients with high uPAR-del4/5 and low TIMP-3 mRNA levels had a highly significantly shorter DFS in comparison to those patients with low uPAR-del4/5 and high TIMP-3 mRNA expression (P < 0.0001). These patients had a more than 6-fold higher risk for disease recurrence or death in multivariate analysis. Therefore, considering the prognostic impact of two proteolytic factors stemming from complementary protease systems may improve the prediction of disease recurrence in breast cancer.

Details

Original languageEnglish
Pages (from-to)2760-2768
Number of pages9
JournalEuropean journal of cancer
Volume41
Issue number17
Publication statusPublished - Nov 2005
Peer-reviewedYes

External IDs

PubMed 16256342

Keywords

Sustainable Development Goals

ASJC Scopus subject areas

Keywords

  • Breast cancer, Prognosis, Quantitative real-time PCR, Tissue inhibitor of metalloproteinase-3, Urokinase receptor transcript variants