Abstract
Background: Whereas the expression of Cathepsin D (Cath D) is suggested to enhance the biological aggressiveness of human malignancies, its role in renal cell carcinoma (RCC), however, has not been investigated. Methods: By tissue microarray analysis, tumor and benign tissue samples from 176 RCC patients were investigated for Cath D expression by immunohistochemistry and Western blots. Expression levels were correlated to clinical variables and to the postoperative outcome. Results: High Cath D expression levels were detected in 29%/9% of tumor and benign tissue samples, respectively (p < 0.0001). In case of a high vs. low Cath D expression level, development of distant metastases was observed in 12% vs. 88% of cases (p < 0.05). With a median follow-up of 50 (2-146) months, high level Cath D expression was correlated with an improved long-term survival when compared with patients presenting with decreased expression [median long-term survival: 82 vs. 53 months in case of a high vs. low expression level] (p < 0.05). Conclusions: The Cath D staining pattern predicted a reduced risk for metastatic spread and tumor dependent death, hereby indicating its role as a biological variable revealing additional prognostic information for renal cell cancer patients. Increased expression of Cath D in tumor vs. benign tissue samples might indicate a role for the development and progression of RCC.
| Original language | English |
|---|---|
| Journal | European Urology |
| Volume | 48 |
| Issue number | 3 |
| Pages (from-to) | 519-526 |
| Number of pages | 8 |
| ISSN | 0302-2838 |
| DOIs | |
| Publication status | Published - 09.2005 |
Funding
The study is supported by a grant from the Federal Ministry of Education and Research (Fö. 01KS9602) and the Interdisciplinary Center of Clinical Research Tuebingen (IZKF). A.S.M. is partly supported by a postgraduate grant from the Novartis Foundation. P.S. is supported by the Fortune program (grant F 1481010).
Research Areas and Centers
- Research Area: Luebeck Integrated Oncology Network (LION)