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Loss of cadherin related family member 5 (CDHR5) expression in clear cell renal cell carcinoma is a prognostic marker of disease progression.
Bläsius, Felix Marius; Meller, Sebastian; Stephan, Carsten; Jung, Klaus; Ellinger, Jörg; Glocker, Michael O; Thiesen, Hans-Jürgen; Tolkach, Yuri; Kristiansen, Glen.
Affiliation
  • Bläsius FM; Institute of Pathology, University Hospital Bonn, Bonn, Germany.
  • Meller S; Institute of Pathology, University Hospital Bonn, Bonn, Germany.
  • Stephan C; Clinic of Urology, Charité-Universitätsmedizin Berlin, Berlin, Germany.
  • Jung K; Berlin Institute for Urologic Research, Robert-Koch Platz 7, Berlin, Germany.
  • Ellinger J; Clinic of Urology, University Hospital Bonn, Bonn, Germany.
  • Glocker MO; Proteome Center Rostock, University of Rostock, Rostock, Germany.
  • Thiesen HJ; Proteome Center Rostock, University of Rostock, Rostock, Germany.
  • Tolkach Y; Institute of Pathology, University Hospital Bonn, Bonn, Germany.
  • Kristiansen G; Institute of Pathology, University Hospital Bonn, Bonn, Germany.
Oncotarget ; 8(43): 75076-75086, 2017 Sep 26.
Article in En | MEDLINE | ID: mdl-29088846
ABSTRACT
Reduced expression of Cadherin-Related Family Member 5 (CDHR5) was recently found implied in carcinogenesis of colon cancer, but its role in other tumors is unknown. We aimed to analyze the expression of CDHR5 in different subtypes of renal cell carcinoma. CDHR5 expression was immunohistochemically examined using tissue micro arrays (TMAs) covering 279 patients with primary renal cell carcinoma. Additionally, expression data from the TCGA (The Cancer Genome Atlas) of an independent cohort of 489 clear-cell RCC cases was evaluated. CDHR5 protein expression was found in 74.9% of cases, with higher levels seen in clear cell and papillary RCC. In the univariate analysis CDHR5 expression was significantly associated with a longer overall survival of RCC patients at the protein (p = 0.026, HR = 0.56) and transcript levels (TCGA-cohort p = 0.0002, HR = 0.55). Importantly, differences in survival times were confirmed independently in multivariate analyses in a model with common clinicopathological variables at the transcript level (p = 0.0097, HR = 0.65). Investigation of the putative functional role of CDHR5 using TCGA data and Enrichment analysis for Gene Ontology and Pathways revealed associations with many metabolic and some tumor growth-associated processes and pathways. CDHR5 expression appears to be a promising and new independent prognostic biomarker in renal cell carcinoma.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Prognostic_studies Language: En Journal: Oncotarget Year: 2017 Document type: Article Affiliation country: Alemania

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Prognostic_studies Language: En Journal: Oncotarget Year: 2017 Document type: Article Affiliation country: Alemania