CircRNA circPDSS1 promotes bladder cancer by down-regulating miR-16
Qinnan Yu1, Pei Liu1, Guangye Han1
1Department of Urology, The First Affiliated Hospital of Xinxiang Medical College, Weihui City, Henan Province 453100, P.R. China.
Bioscience Reports
|December 24, 2019
Summary
Circular RNA circPDSS1 is elevated in urothelial bladder cancer (UBC) and promotes cancer progression by down-regulating miR-16. This finding suggests circPDSS1 as a potential therapeutic target for UBC.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Circular RNA (circRNA) circPDSS1, an identified oncogene in gastric cancer, has unknown roles in other cancers.
- This study investigates the function of circPDSS1 in urothelial bladder cancer (UBC).
Purpose of the Study:
- To elucidate the role of circPDSS1 in the development and progression of urothelial bladder cancer (UBC).
- To investigate the relationship between circPDSS1 and miR-16 in UBC.
- To assess the potential of circPDSS1 as a therapeutic target for UBC.
Main Methods:
- Gene expression levels of circPDSS1 and miR-16 were measured using RT-qPCR in 72 UBC patient biopsies and UBC cell lines (HT-1197, UMUC3).
- Cell transfections were performed to manipulate circPDSS1 and miR-16 expression.
- Functional assays including proliferation, migration, and invasion assays were conducted to evaluate the impact of circPDSS1 and miR-16 on UBC cell behavior.
Main Results:
- circPDSS1 was found to be significantly up-regulated in UBC tissues, with expression levels correlating with advanced clinical stages.
- circPDSS1 overexpression led to increased proliferation, migration, and invasion of UBC cells.
- circPDSS1 was found to down-regulate miR-16, and miR-16 overexpression inhibited UBC cell proliferation, migration, and invasion, while also attenuating the effects of circPDSS1.
Conclusions:
- circRNA circPDSS1 promotes UBC progression, potentially by down-regulating miR-16.
- circPDSS1 represents a potential oncogene and therapeutic target in urothelial bladder cancer.
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