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Updated: Nov 28, 2025

miRNA Expression Analyses in Prostate Cancer Clinical Tissues
Published on: September 8, 2015
Silencing circSLC19A1 Inhibits Prostate Cancer Cell Proliferation, Migration and Invasion Through Regulating
Banggao Huang1, Danhong Zhou2, Xinmian Huang1
1Department of Urology, Zhejiang Provincial People's Hospital, Hangzhou, Zhejiang Province, People's Republic of China.
Background:
Emerging evidence indicates that circular RNAs (circRNAs), which form as covalently closed loops, play a regulatory role in various types of cancer, including prostate cancer (PCa). CircSLC19A1, one kind of circRNA, was subjected to the study and its role in PCa was explored.
Methods:
Expressions of circSLC19A1, miR-326 and MAPK1 in PCa tissues and cells were assessed by qRT-PCR. CircSLC19A1 was identified by RNase R treatment. The binding relations between circSLC19A1 and miR-326 and between miR-326 and MAPK1 were predicted by RegRNA2.0 or Targetscan7.2 and further confirmed by dual-luciferase reporter assay. Pearson correlation analysis of the correlation among circSLC19A1, miR-326 and MAPK1 was performed. CCK-8, cell colony formation, wound healing and Transwell assays were used to assess PCa cell viability, proliferation, migration and invasion, respectively.
Results:
CircSLC19A1 expression was up-regulated in PCa tissue and cell cytoplasm. Silencing circSLC19A1 inhibited PCa cell viability, proliferation, migration, invasion and miR-326 expression. MiR-326 inhibitor promoted the luciferase activities of circSLC19A1 and MAPK1, increased MAPK1 expression and facilitated PCa cell progression. MiR-326 expression was down-regulated in PCa tissue and there was a negative correlation between miR-326 and circSLC19A1 expressions. MAPK1 expression was up-regulated in PCa tissue. There was a negative correlation between MAPK1 and miR-326 expressions as well as a positive correlation between MAPK1 and circSLC19A1 expressions. Silencing MAPK1 promoted the viability, proliferation, migration, and invasion of PCa cells co-transfected with siRNA-circSLC19A1a and miR-326 inhibitor.
Conclusion:
CircSLC19A1 silencing inhibited PCa cell proliferation, migration and invasion through regulating miR-326/MAPK1 axis.
Insights
Circular RNA (circRNA) circSLC19A1 is upregulated in prostate cancer (PCa). Silencing circSLC19A1 inhibits PCa progression by regulating the miR-326/MAPK1 axis, offering a potential therapeutic target for PCa.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Circular RNAs (circRNAs) are increasingly recognized for their regulatory roles in cancer.
- Prostate cancer (PCa) is a significant area of research within oncology.
- CircSLC19A1 has emerged as a specific circRNA of interest for its potential involvement in PCa pathogenesis.
Purpose of the Study:
- To investigate the role and mechanism of circSLC19A1 in prostate cancer (PCa).
- To explore the regulatory relationship between circSLC19A1, miR-326, and MAPK1 in PCa cells.
Main Methods:
- Quantitative real-time PCR (qRT-PCR) to assess gene expression levels.
- RNase R treatment to confirm circRNA identification.
- Dual-luciferase reporter assays to validate binding interactions.
- Cellular assays including CCK-8, colony formation, wound healing, and Transwell assays to evaluate cell behavior.
Main Results:
- CircSLC19A1 expression was significantly upregulated in PCa tissues and cells.
- Silencing circSLC19A1 suppressed PCa cell viability, proliferation, migration, and invasion.
- A regulatory axis involving circSLC19A1, miR-326, and MAPK1 was identified, with circSLC19A1 positively correlating with MAPK1 and negatively with miR-326.
Conclusions:
- CircSLC19A1 acts as an oncogenic circRNA in prostate cancer.
- CircSLC19A1 silencing inhibits PCa cell proliferation, migration, and invasion.
- The findings highlight the circSLC19A1/miR-326/MAPK1 pathway as a potential therapeutic target for PCa treatment.
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