Abstract

Increased knowledge of the molecular differences between indolent and aggressive prostate cancer is needed for improved risk stratification and treatment selection. Secreted frizzled-related protein 4 (SFRP4) is a modulator of the cancer-associated Wnt pathway, and previously suggested as a potential marker for prostate cancer aggressiveness. In this study, we investigated and validated the association between SFRP4 gene expression and aggressiveness in nine independent cohorts (n = 2157). By differential expression and combined meta-analysis of all cohorts, we detected significantly higher SFRP4 expression in cancer compared with normal samples, and in high (3–5) compared with low (1–2) Grade Group samples. SFRP4 expression was a significant predictor of biochemical recurrence in six of seven cohorts and in the overall analysis, and was a significant predictor of metastatic event in one cohort. In our study cohort, where metabolic information was available, SFRP4 expression correlated significantly with the concentrations of citrate and spermine, two previously suggested biomarkers for aggressive prostate cancer. SFRP4 immunohistochemistry in an independent cohort (n = 33) was not associated with aggressiveness. To conclude, high SFRP4 gene expression is associated with high Grade Group and recurrent prostate cancer after surgery. Future studies investigating the mechanistic and clinical usefulness of SFRP4 in prostate cancer are warranted.

Highlights

  • Prostate cancer is the second most common cancer and the fifth leading cause of cancer related death in men worldwide[1]

  • We showed Secreted frizzled-related protein 4 (SFRP4) expression to be increased in prostate cancer, and further increased in high Grade Group (3–5) compared with low Grade Group (1–2) cancers

  • SFRP4 gene expression was found to be a predictor of worse outcome in prostatectomy-treated prostate cancer patients

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Summary

Introduction

Prostate cancer is the second most common cancer and the fifth leading cause of cancer related death in men worldwide[1]. SFRP4 has been included in different gene expression signatures linked to prostate cancer aggressiveness and recurrence[10,11], including our previously published signature for non-canonical Wnt pathway and epithelial-to-mesenchymal transition (NCWP-EMT) markers[12]. The metabolites citrate and spermine have shown promise as biomarkers and are found in lower concentrations in aggressive compared to indolent cancers[16,17]. Reduced concentrations of these metabolites[12], but the correlation between SFRP4 gene and protein expression levels, and citrate and spermine has not previously been investigated in prostate cancer. The overall aim of this study was to investigate and validate SFRP4 gene expression in prostate cancer, and its relation to cancer aggressiveness. The results were validated in eight independent, publically available gene expression prostate cancer cohorts with patient follow-up data. Our approach of including several independent patient cohorts gave increased statistical power, and improved the accuracy and generalisation of the results

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