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Sequencing Small Non-coding RNA from Formalin-fixed Tissues and Serum-derived Exosomes from Castration-resistant Prostate Cancer Patients
Published on: November 19, 2019
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[Primary candidate rna biomarker screening by RNA-seq for prostate cancer diagnostics]
A S Nikitina1, V V Babenko2, K A Babalyan3
1Federal Research and Clinical Center of Physical-Chemical Medicine, Moscow, Russia; Moscow Institute of Physics and Technology, Dolgoprudniy, Russia.
Biomeditsinskaia Khimiia
|December 31, 2015
Summary
RNA sequencing successfully identified prostate cancer biomarkers in urine and plasma, even in benign prostatic hyperplasia (BPH) cases. Further research is needed to confirm specificity for accurate, minimally invasive prostate cancer diagnostics.
Area of Science:
- Molecular Biology
- Oncology
- Biomarker Discovery
Context:
- Prostate cancer diagnosis often relies on invasive procedures.
- Minimally invasive methods for detecting prostate cancer biomarkers are highly desirable.
- RNA biomarkers in bodily fluids offer a promising avenue for noninvasive screening.
Purpose:
- To evaluate the feasibility of using RNA sequencing (RNA-seq) to screen for prostate cancer RNA biomarkers in plasma and urine.
- To assess the presence of known prostate cancer RNA biomarkers in samples from patients with benign prostatic hyperplasia (BPH).
- To investigate the influence of library preparation methods on biomarker detection.
Summary:
- RNA-seq is a feasible approach for screening prostate cancer RNA biomarkers in plasma and urine.
- Significant numbers of prostate cancer-associated RNA biomarkers were detected in both plasma and urine samples from BPH patients.
- The number of detected RNA biomarkers varied depending on the library preparation method used for transcriptome profiling.
- The presence of these biomarkers in BPH samples indicates a potential lack of specificity, necessitating further investigation.
Impact:
- Demonstrates the potential of RNA-seq in plasma and urine for minimally invasive prostate cancer diagnostics.
- Highlights the need for rigorous validation to ensure the specificity of identified RNA biomarkers.
- Suggests that RNA biomarker profiles may differ between prostate cancer and BPH, requiring further research to differentiate.

