4.2 Article

MiR-34b-3p Represses the Multidrug-Chemoresistance of Bladder Cancer Cells by Regulating the CCND2 and P2RY1 Genes

Journal

MEDICAL SCIENCE MONITOR
Volume 25, Issue -, Pages 1323-1335

Publisher

INT SCIENTIFIC INFORMATION, INC
DOI: 10.12659/MSM.913746

Keywords

Drug Resistance; MicroRNAs; Urinary Bladder Neoplasms

Funding

  1. Innovation Program of Science and Technology Bureau of Hefei [81572350]
  2. Youth Technical Backbone Fund of West Branch of the First Affiliated Hospital of USTC

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Background: Chemoresistance is a main limitation in chemotherapy for therapeutic cancer. MicroRNA (miRNA) has been indicated in the progression and tumorigenesis of many types of cancer, but the effect of miR-34b-3p in bladder cancer (BCa) cells is still unknown. Material/Methods: This research compared the multidrug-sensitive (5637) BCa cell line and the multidrug-resistant (EJ) BCa cell line. We found that CCND2 (G1/S-specific cyclin-D2) and P2RY1 (purinergic receptor P2Y1) were the targets of miR-34b-3p, as further validated by qRT-PCR (quantitative real-time polymerase chain reaction) and western blot analysis. Results: Forced reversal of the levels of miR-34b-3p or CCND2/P2RY1 changed the chemoresistance profiles in both 5637 cells and EJ cells. Further experiments suggested that the CCND2 gene and the P2RY1 gene act in concert to negatively correlate with miR-34b-3p effect on BCa multidrug-chemoresistance. Conclusions: These results not only reveal new players regulating BCa chemoresistance, but also provide clues for effective chemotherapy for BCa patients.

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