snRNAs from Radical Prostatectomy Specimens Have the Potential to Serve as Prognostic Factors for Clinical Recurrence after Biochemical Recurrence in Patients with High-Risk Prostate Cancer

Author:

Mikami Hikaru1,Noguchi Syunya2,Akatsuka Jun1,Hasegawa Hiroya1,Obayashi Kotaro1,Takeda Hayato1,Endo Yuki1ORCID,Toyama Yuka1,Takei Hiroyuki3ORCID,Kimura Go1ORCID,Kondo Yukihiro1,Takizawa Toshihiro2

Affiliation:

1. Department of Urology, Nippon Medical School Hospital, Tokyo 113-8603, Japan

2. Department of Molecular Medicine and Anatomy, Nippon Medical School, Tokyo 113-8602, Japan

3. Department of Breast Surgical Oncology, Nippon Medical School, Tokyo 113-8602, Japan

Abstract

In patients with high-risk prostate cancer (HRPC) after radical prostatectomy (RP), biochemical recurrence (BCR) increases the risk of distant metastasis. Accordingly, additional prognostic biomarkers are required to identify the subpopulation of patients with HRPC who develop clinical recurrence (CR) after BCR. The objective of this study was to identify biomarkers in formalin-fixed paraffin-embedded (FFPE) RP samples that are prognostic for CR in patients with HRPC who experience BCR after RP (post-RP BCR). First, we performed a preliminary RNA sequencing analysis to comprehensively profile RNA expression in FFPE RP samples obtained from patients with HRPC who developed CR after post-RP BCR and found that many snRNAs were very abundant in preserved FFPE samples. Subsequently, we used quantitative polymerase chain reaction (qPCR) to compare the expression levels of highly abundant snRNAs in FFPE RP samples from patients with HRPC with and without CR after post-RP BCR (21 CR patients and 46 non-CR patients who had more than 5 years of follow-up after BCR). The qPCR analysis revealed that the expression levels of snRNA RNU1-1/1-2 and RNU4-1 were significantly higher in patients with CR than in patients without CR. These snRNAs were significantly correlated with clinical recurrence-free survival (RFS) in patients with HRPC who experienced post-RP BCR. Furthermore, snRNA RNU1-1/1-2 could serve as an independent prognostic factor for clinical RFS in post-RP BCR of HRPC cases where known prognostic factors (e.g., Gleason score) cannot distinguish between CR and non-CR patients. Our findings provide new insights into the involvement of snRNAs in prostate cancer progression.

Funder

Grants-in-Aid for Scientific Research

Nippon Medical School Grant-in-Aid for Medical Research

Publisher

MDPI AG

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