4.4 Article

circ3323 Motivates Host Gene to Promote the Aggressiveness of Bladder Cancer

Journal

BIOCHEMICAL GENETICS
Volume 60, Issue 6, Pages 2327-2345

Publisher

SPRINGER/PLENUM PUBLISHERS
DOI: 10.1007/s10528-022-10210-x

Keywords

Bladder cancer; Malignant progression; miRNA-186; circ3323

Funding

  1. Changzhou Science and Technology Bureau [WZ201931]

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In this study, a novel circRNA (circ3323) was identified and its role in the progression of bladder cancer (BCa) was investigated. It was found that circ3323 modulates the metastasis of BCa through the regulation of the miR-186-5p/APP axis, and its expression level is closely associated with the prognosis of BCa patients.
Bladder cancer (BCa) is the most common cancer in the urinary system with high recurrence rate and poor prognosis. Circular RNA (circRNA) is a novel subclass of noncoding-RNA which participate in progression of BCa. Here, we identified a novel circRNA-circ3323 and aimed to investigate the role of circ3323 in progression of BCa. Public data of RNA sequencing was used to identify significant circRNA related to BCa. The role of circRNAs in progression of BCa was assessed in cytotoxicity assay, transwell assay and flow cytometry. Biotin-coupled RNA pull-down and fluorescence in situ hybridization were performed to evaluate the interaction between circRNAs and miRNAs. The expression of circ3323 was higher in BCa tissues and cells than in normal samples. Experiments in vitro showed that the knockdown of circ3323 inhibited cell proliferation and impeded the metastasis of BCa cells. Mechanistically, we demonstrated that circ3323 acts as a sponge for miR-186-5p and promotes host gene APP's expression. Clinically, circ3323 predicts worse overall survival of BCa patients, indicating its prognostic value. Our study identified that circ3323 modulates metastasis of BCa through miR-186-5p/APP axis and may serve as a promising prognostic biomarker for BCa, which provides novel insights into treatment of BCa.

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