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Updated: Nov 30, 2025

miRNA Expression Analyses in Prostate Cancer Clinical Tissues
Published on: September 8, 2015
Hsa_circ_0088233 Alleviates Proliferation, Migration, and Invasion of Prostate Cancer by Targeting hsa-miR-185-3p
Zhi-Hai Deng1, Gan-Shen Yu2, Ke-Lei Deng3
1Department of Urology, Gaozhou People's Hospital, Gaozhou, China.
Abstract:
Prostate cancer is the most common malignant tumor of the urinary system. The mechanisms of the initiation and progression of prostate cancer have not been fully elucidated. Increasing evidence suggests that circular RNAs (circRNAs) are involved in cancer pathogenesis. In this study, we aimed to identify differentially expressed circRNAs in prostate cancer tissues and explored the role of circRNAs in the pathogenesis of prostate cancer. By screening a circRNA microarray assay, we found that circ_0088233 was upregulated in prostate cancer tissues compared to adjacent normal tissues, and this upregulation can be verified in 46 pairs of prostate cancer and adjacent normal tissues examined using quantitative reverse transcription-PCR. The level of circ_0088233 correlated with the TNM stage. Knockdown of circ_0088233 reduced cell proliferation, migration, invasion, and induced G1 phase arrest and apoptosis. In addition, miR-185-3p was identified as the downstream target of circ_0088233 using luciferase reporter assays and a biotinylated circ_0088233 probe pull-down assay. The miR-185-3p level showed a negative correlation with the circ_0088233 level in prostate cancer tissues. Overexpression of circ_0088233 blocked the effects of miR-185-3p on cell proliferation, migration, invasion, cell cycle, and apoptosis. In conclusion, circ_0088233 may function as an oncogene and play an oncogenic role by sponging hsa-miR-185-3p. This study increases the understanding of circRNAs in the progression of prostate cancer. These results implicate circ_0088233 as a potential therapeutic target for prostate cancer.
Insights
Circular RNAs (circRNAs) like circ_0088233 are upregulated in prostate cancer and promote tumor growth. Targeting circ_0088233 may offer a new therapeutic strategy for prostate cancer patients.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Prostate cancer pathogenesis remains incompletely understood.
- Circular RNAs (circRNAs) are increasingly implicated in cancer development.
- The specific role of circRNAs in prostate cancer requires further investigation.
Purpose of the Study:
- To identify differentially expressed circRNAs in prostate cancer.
- To explore the functional role of circRNAs in prostate cancer progression.
- To investigate circ_0088233 as a potential therapeutic target.
Main Methods:
- circRNA microarray screening.
- Quantitative reverse transcription-PCR (qRT-PCR) validation.
- Cell proliferation, migration, invasion, cell cycle, and apoptosis assays.
- Luciferase reporter and pull-down assays to identify miRNA targets.
Main Results:
- circ_0088233 was significantly upregulated in prostate cancer tissues and correlated with TNM stage.
- Knockdown of circ_0088233 inhibited proliferation, migration, invasion, and induced apoptosis.
- circ_0088233 acts as a sponge for miR-185-3p, inhibiting its tumor-suppressive effects.
- circ_0088233 functions as an oncogene in prostate cancer.
Conclusions:
- circ_0088233 promotes prostate cancer progression by sponging miR-185-3p.
- circ_0088233 is a potential diagnostic biomarker and therapeutic target for prostate cancer.
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