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3-D Cell Culture System for Studying Invasion and Evaluating Therapeutics in Bladder Cancer
Published on: September 13, 2018
MicroRNA-93 promotes bladder cancer proliferation and invasion by targeting PEDF
Hua Jiang1, Qiang Bu1, Minghui Zeng1
1Department of Urology, People's Hospital of Danyang, Jiangsu, China.
Objective:
MicroRNA-93 (miR-93) is upregulated in the urine of patients with bladder cancer (BC). Here, we investigated the role of miR-93 in BC progression and explored the underlying mechanism.
Methods:
miR-93 expression in BC tissues and cells was detected by real time-polymerase chain reaction. The effects of miR-93 and pigment epithelium-derived factor (PEDF) on cell proliferation and invasion were assessed using the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide and Transwell assays. The binding of miR-93 to the 3'-untranslated region of PEDF was identified by the luciferase reporter assay.
Results:
miR-93 expression was higher in BC tissues than in normal controls, and its expression was associated with tumor stage and node stage. Inhibition of miR-93 suppressed the proliferation and invasion of BC cells. PEDF was identified as a target of miR-93 and shown to mediate the effect of miR-93 on cell proliferation and invasion.
Conclusions:
The present data suggested that miR-93 promoted BC cell proliferation and invasion by targeting PEDF, providing new biomarkers and targets for BC diagnosis and treatment.
Insights
MicroRNA-93 (miR-93) promotes bladder cancer (BC) cell growth and spread by targeting pigment epithelium-derived factor (PEDF). This finding offers potential new biomarkers and therapeutic targets for BC.
Area of Science:
- Oncology
- Molecular Biology
- Biochemistry
Background:
- Bladder cancer (BC) is a significant global health concern.
- MicroRNA-93 (miR-93) has been observed to be upregulated in BC patients' urine.
- The precise role and mechanism of miR-93 in BC progression require further elucidation.
Purpose of the Study:
- To investigate the role of miR-93 in bladder cancer (BC) progression.
- To explore the underlying molecular mechanisms by which miR-93 influences BC.
- To identify potential diagnostic and therapeutic targets for BC.
Main Methods:
- Quantitative real-time polymerase chain reaction (qRT-PCR) was used to measure miR-93 expression in BC tissues and cells.
- Cell proliferation was assessed using the MTT assay, and cell invasion was evaluated using Transwell assays.
- The interaction between miR-93 and pigment epithelium-derived factor (PEDF) was confirmed via luciferase reporter assays.
Main Results:
- miR-93 expression was significantly elevated in BC tissues compared to normal controls.
- Higher miR-93 levels correlated with advanced tumor and node stages in BC patients.
- Inhibition of miR-93 notably reduced BC cell proliferation and invasion.
- Pigment epithelium-derived factor (PEDF) was identified as a direct target of miR-93, mediating its effects on cell behavior.
Conclusions:
- miR-93 promotes bladder cancer cell proliferation and invasion through the targeting of PEDF.
- These findings highlight miR-93 as a potential biomarker for BC diagnosis.
- Targeting the miR-93/PEDF pathway presents a promising therapeutic strategy for bladder cancer.
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