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CircZNF609 promotes bladder cancer progression and inhibits cisplatin sensitivity via miR-1200/CDC25B pathway
Dexiang Feng1, Jiancheng Lv1, Kai Li1
1Department of Urology, The First Affiliated Hospital of Nanjing Medical University, Nanjing, 210029, China.
Abstract:
Circular RNAs (circRNAs) have been extensively studied in tumor development and treatment. CircZNF609 (hsa_circ_0000615) has been shown to serve as an oncogene in all kinds of solid tumors and may act as the novel biomarker in tumor diagnosis and therapy in tumor early diagnosis and therapy. However, the underlying character and mechanism of circZNF609 in cisplatin chemosensitivity and bladder cancer (BCa) development were unknown. The expression level of cell division cycle 25B (CDC25B), microRNA 1200 (miR-1200), and circZNF609 in BCa cells and tissues depended on quantitative real-time PCR (qRT-PCR). CDC25B protein level was assayed with Western blot. Functional assays in vitro and in vivo had been conducted to inspect the important role of circZNF609 on BCa progression and cisplatin chemosensitivity in BCa. RNA sequencing and online databases were used to predict the interactions among circZNF609, miR-1200, and CDC25B. Mechanistic exploration was confirmed by RNA pull-down assay, RNA fluorescence in situ hybridization (FISH) and Dual luciferase reporter assay. CircZNF609 expression was increased significantly in BCa cell lines and tissues. For BCa patients, increased expression of circZNF609 was correlated with a worse survival. In vitro and in vivo, enforced expression of circZNF609 enhanced BCa cells proliferation, migration, and cisplatin chemoresistance. Mechanistically, circZNF609 alleviated the inhibition effect on target CDC25B expression by sponging miR-1200. CircZNF609 promoted tumor growth through novel circZNF609/miR-1200/CDC25B axis, implying that circZNF609 has significant potential to act as a new diagnostic biomarker and therapeutic target in BCa. Enhancing cisplatin sensitivity is an important direction for bladder cancer management. 1. This research reveals that circZNF609 improves bladder cancer progression and inhibits cisplatin sensitivity by inducing G1/S cell cycle arrest via a novel miR-1200/CDC25B cascades. 2. CircZNF609 was confirmed associated with worse survival of bladder cancer patients. 3. CircZNF609 act as a prognostic biomarker for bladder cancer treatment.
Insights
Circular RNA ZNF609 (circZNF609) promotes bladder cancer progression and reduces cisplatin sensitivity by regulating the miR-1200/CDC25B pathway. CircZNF609 may serve as a prognostic biomarker for bladder cancer treatment.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Circular RNAs (circRNAs) are implicated in tumor development and treatment.
- CircZNF609 (hsa_circ_0000615) is recognized as an oncogene in solid tumors and a potential biomarker.
- The specific role of circZNF609 in bladder cancer (BCa) and its impact on cisplatin chemosensitivity remain unclear.
Purpose of the Study:
- To investigate the role and mechanism of circZNF609 in bladder cancer progression.
- To explore the relationship between circZNF609 and cisplatin chemosensitivity in bladder cancer.
- To assess circZNF609 as a potential diagnostic and therapeutic target for bladder cancer.
Main Methods:
- Quantitative real-time PCR (qRT-PCR) and Western blot were used to measure circZNF609, miR-1200, and CDC25B levels.
- In vitro and in vivo functional assays evaluated circZNF609's impact on BCa progression and chemosensitivity.
- RNA sequencing, bioinformatics, RNA pull-down, FISH, and dual luciferase assays elucidated the molecular mechanism.
Main Results:
- CircZNF609 expression was significantly elevated in BCa cell lines and tissues, correlating with poorer patient survival.
- Overexpression of circZNF609 enhanced BCa cell proliferation, migration, and cisplatin resistance in vitro and in vivo.
- CircZNF609 acts as a molecular sponge for miR-1200, thereby upregulating CDC25B expression and promoting tumor growth via the circZNF609/miR-1200/CDC25B axis.
Conclusions:
- CircZNF609 promotes bladder cancer progression and reduces cisplatin sensitivity by inhibiting G1/S cell cycle arrest through the novel miR-1200/CDC25B pathway.
- Elevated circZNF609 levels are associated with worse survival in bladder cancer patients.
- CircZNF609 shows significant potential as a prognostic biomarker and therapeutic target for bladder cancer.
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