Novel urine-enriched RNA panel (EPCAM, TTC3, H4C5) to detect prostate cancer and differentiate it from benign prostatic disease.
31 Background: Prostate Cancer (PCa) is one of the leading causes of cancer deaths among men worldwide. Although the Prostate-Specific Antigen (PSA) test is widely used for screening, several advisory groups recommend against PSA because of its non-specific and suboptimal performance. Hence, there is an urgent unmet need for novel and more accurate biomarker panels for PCa detection. Methods: To develop an alternate assay, we collected voided urine (50 ml) from 236 pre- and 198 matched post-prostatectomy men with PCa, 76 benign prostatic hyperplasia (BPH), 21 prostatitis and 107 normal healthy men between the years 40-80. We isolated RNA from exfoliated cells and debris shed into urine, subjected to deep-sequencing of 50 selected genes (adj P value < 0.05 and log FC > 2), and performed advanced machine-learning approaches to discover potential biomarkers in men with PCa. Results: From 50 RNAs initially tested in 20 pooled urine samples, 3 RNAs (EPCAM, TTC3, H4C5) were identified to detect men with PCa robustly (with higher specificity and sensitivity) and distinguished them between pre- and post-prostatectomy in PCa patients. The biomarkers, in combination, outperformed a known urinary RNA marker, PCA3 (area under the curve, 0.96, Figure 1 left). Immunohistochemistry and qPCR analysis in prostate FFPE tissues further confirmed that the origin of these three biomarkers is prostate-specific. In addition, the biomarker panel could separate PCa from benign prostatic disease (area under the curve, 0.89), where both diseases show a higher elevation of PSA. TTC3 and EpCAM gene silencing in PCa cells showed a tumor suppression in vitro and in vivo , suggesting its relevance to PCa development. Conclusions: The urine-based RNA biomarker panel (EPCAM, TTC3, H4C5) is a promising noninvasive diagnostic tool to separate PCa from BPH/prostatitis and healthy individuals; further prospective validation is warranted.
Authors
- Vipul Patel (ORCID: https://orcid.org/0000-0002-7012-5752)
- Márcio Covas Moschovas (ORCID: https://orcid.org/0000-0002-3290-7323)
- Guru Sonpavde (ORCID: https://orcid.org/0000-0002-1010-9611)
- Bongyong Lee (ORCID: https://orcid.org/0000-0003-3134-7093)
- Ranjan J. Perera (ORCID: https://orcid.org/0000-0002-5926-3687)
- Roshane Perera
- Christian P. Pavlovich (ORCID: https://orcid.org/0000-0002-8532-0251)
- Ernest K. Amankwah (ORCID: https://orcid.org/0000-0001-7054-9400)
- Kandarp Joshi (ORCID: https://orcid.org/0000-0002-2153-0110)
- Menglang Yuan
Institutions
- Johns Hopkins University (US)
- Johns Hopkins Medicine (US)
- AdventHealth Celebration (US)
- Florida Hospital Cancer Institute (US)
- Johns Hopkins All Children's Hospital (US)
Publication Details
- Journal
- Journal of Clinical Oncology
- Published
- 2025-02-10
- DOI
- https://doi.org/10.1200/jco.2025.43.5_suppl.31
- Primary Topic
- RNA modifications and cancer
- Type
- article
- Field-Weighted Citation Impact
- 0.00