Clinical implications of AGR2 in primary prostate cancer: Results from a large‐scale study

Author:

Wambach Moritz1,Montani Matteo2,Runz Josefine3,Stephan Carsten4,Jung Klaus4,Moch Holger3,Eberli Daniel5,Bernhardt Marit1,Hommerding Oliver1,Kreft Tobias1,Cronauer Marcus V.1,Kremer Anika1,Mayr Thomas1,Hauser Stefan6,Kristiansen Glen1ORCID

Affiliation:

1. Institute of Pathology University Hospital Bonn Bonn Germany

2. Institute of Pathology University Hospital Bern Bern Switzerland

3. Department of Pathology and Molecular Pathology University Hospital Zurich and University Zurich Zurich Switzerland

4. Department of Urology Charité University Hospital Berlin Germany

5. Clinic of Urology University Hospital Zurich Zurich Switzerland

6. Clinic of Urology University Hospital Bonn Bonn Germany

Abstract

Human anterior gradient‐2 (AGR2) has been implicated in carcinogenesis of various solid tumours, but the expression data in prostate cancer are contradictory regarding its prognostic value. The objective of this study is to evaluate the expression of AGR2 in a large prostate cancer cohort and to correlate it with clinicopathological data. AGR2 protein expression was analysed immunohistochemically in 1023 well‐characterized prostate cancer samples with a validated antibody. AGR2 expression levels in carcinomas were compared with matched tissue samples of adjacent normal glands. AGR2 expression levels were dichotomized and tested for statistical significance. Increased AGR2 expression was found in 93.5% of prostate cancer cases. AGR2 levels were significantly higher in prostate cancer compared with normal prostate tissue. A gradual loss of AGR2 expression was associated with increasing tumour grade (ISUP), and AGR2 expression is inversely related to patient survival, however, multivariable significance is not achieved. AGR2 is clearly upregulated in the majority of prostate cancer cases, yet a true diagnostic value appears unlikely. In spite of the negative correlation of AGR2 expression with increasing tumour grade, no independent prognostic significance was found in this large‐scale study.

Publisher

Wiley

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