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.

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.