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Updated: Nov 22, 2025

MicroRNA Detection in Prostate Tumors by Quantitative Real-time PCR qPCR
Published on: May 16, 2012
Downregulation of circ-TRPS1 suppressed prostatic cancer prognoses by regulating miR-124-3p/EZH2 axis-mediated
Jianjun Sha1, Lei Xia1, Qing Han2
1Department of Urology, Renji Hospital, School of Medicine, Shanghai Jiaotong University Shanghai 200127, China.
Abstract:
Abnormal circular RNA (circRNA) expression correlates with human traits such as many kinds of cancers. Though circRNAs have links to cancer, they have less characterization in metastatic castration-resistant prostate cancer (PCa), which is main reason for PCa mortality. Therefore, high-throughput sequencing was used for selected circRNA profiles. The result showed that circ-TRPS1 was upregulated significantly in high-grade PCa tissues or cell lines. High circ-TRPS1 expression correlated to aggressive PCa phenotypes. Knockdown of circ-TRPS1 suppressed PCa proliferation and metastasis through targeting miR-124-3p/EZH2 axis-mediated stemness in PCa, which was validated by luciferase reporter assays. EZH2 overexpression or miR-124-3p inhibition reversed the inhibition of circ-TRPS1 silencing in PCa cell migration and proliferation by recovering stemness. In summary, data demonstrated that circ-TRPS1 suppressed PCa progression through functioning similar to a miR-124-3p sponge to enhance EZH2 expression and cancer stem-like cell differentiation. Thus, circ-TRPS1 might be a candidate target for PCa treatment.
Insights
Circular RNAs (circRNAs) are linked to cancer. This study found circ-TRPS1 is upregulated in prostate cancer (PCa), driving its progression by targeting the miR-124-3p/EZH2 axis.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Abnormal circular RNA (circRNA) expression is associated with various cancers.
- circRNAs are under-characterized in metastatic castration-resistant prostate cancer (PCa), a leading cause of PCa mortality.
Purpose of the Study:
- To investigate the role of circRNAs in prostate cancer progression.
- To identify potential therapeutic targets for PCa treatment.
Main Methods:
- High-throughput sequencing to profile circRNAs in PCa tissues and cell lines.
- circRNA knockdown experiments to assess functional impact on PCa phenotypes.
- Luciferase reporter assays to validate molecular interactions.
Main Results:
- circ-TRPS1 was significantly upregulated in high-grade PCa tissues and cell lines.
- High circ-TRPS1 expression correlated with aggressive PCa phenotypes.
- Knockdown of circ-TRPS1 suppressed PCa proliferation and metastasis via the miR-124-3p/EZH2 axis, affecting stemness.
Conclusions:
- circ-TRPS1 acts as a miR-124-3p sponge, enhancing EZH2 expression and promoting cancer stem-like cell differentiation.
- circ-TRPS1 plays a crucial role in suppressing PCa progression.
- circ-TRPS1 represents a potential therapeutic target for prostate cancer.
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