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Analysis of Combinatorial miRNA Treatments to Regulate Cell Cycle and Angiogenesis
Published on: March 30, 2019
LncRNA growth arrest-specific transcript 5 targets miR-21 gene and regulates bladder cancer cell proliferation and
Dong Chen1, Yihong Guo1, Yaqiu Chen1
1Department of Urology, The Second Affiliated Hospital of Fujian Medical University, Quanzhou, China.
Abstract:
The aim of this study was to investigate the mechanism by which growth arrest-specific transcript 5 (GAS5) regulates bladder cancer cells. Bladder cancer samples were collected and tested for experiment. Dual-luciferase reporter assay was used to verify the downstream target genes for GAS5 and miR-21. The expression level of GAS5 was decreased and that of miR-21 was increased, indicating a negative correlation between the two. Patients with high GAS5 level and low miR-21 level had relatively longer survival rates. GAS5 inhibited bladder cancer cells proliferation and promoted apoptosis, and miR-21 had the opposite effects. MiR-21 was a direct target for GAS5, whereas phosphatase and tensin homolog (PTEN) was a direct target gene of miR-21. Low expression of miR-21 could reverse the proliferative and antiapoptotic effects caused by GAS5 silencing. High levels of GAS5 and low levels of miR-21 might be associated with a higher survival rate in bladder cancer patients. GAS5 could exert antiproliferative and proapoptotic effects on bladder cancer cells through miR-21 and PTEN.
Insights
Growth arrest-specific transcript 5 (GAS5) inhibits bladder cancer progression by downregulating miR-21, a key factor in cell proliferation and survival. This suggests GAS5 and low miR-21 levels are linked to better patient outcomes.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Bladder cancer remains a significant health concern with complex regulatory mechanisms.
- Growth arrest-specific transcript 5 (GAS5) is a long non-coding RNA implicated in various cellular processes.
- Understanding the role of GAS5 in bladder cancer is crucial for developing targeted therapies.
Purpose of the Study:
- To elucidate the regulatory mechanism of GAS5 in bladder cancer cells.
- To investigate the interaction between GAS5, miR-21, and PTEN in bladder cancer.
- To correlate GAS5 and miR-21 expression levels with patient survival rates.
Main Methods:
- Analysis of bladder cancer patient samples.
- Dual-luciferase reporter assays to identify downstream targets of GAS5 and miR-21.
- Quantitative assessment of GAS5 and miR-21 expression levels.
- In vitro assays to evaluate effects on cell proliferation and apoptosis.
Main Results:
- GAS5 expression was inversely correlated with miR-21 expression in bladder cancer tissues.
- GAS5 demonstrated inhibitory effects on bladder cancer cell proliferation and promoted apoptosis.
- miR-21 was identified as a direct target of GAS5, and PTEN as a direct target of miR-21.
- High GAS5 and low miR-21 levels correlated with improved patient survival.
Conclusions:
- GAS5 exerts antiproliferative and proapoptotic effects on bladder cancer cells via the miR-21/PTEN pathway.
- The GAS5/miR-21/PTEN axis represents a potential therapeutic target for bladder cancer.
- GAS5 and miR-21 levels may serve as prognostic biomarkers for bladder cancer patients.
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