CircHIPK3 sponges miR-558 to suppress heparanase expression in bladder cancer cells.
Yawei LiFuxin ZhengXingyuan XiaoFei XieDan TaoChao HuangDong LiuMiao WangLiang WangFuqing ZengGuosong JiangPublished in: EMBO reports (2017)
Increasing evidences suggest that circular RNAs (circRNAs) exert crucial functions in regulating gene expression. In this study, we perform RNA-seq and identify 6,154 distinct circRNAs from human bladder cancer and normal bladder tissues. We find that hundreds of circRNAs are significantly dysregulated in human bladder cancer tissues. We further show that circHIPK3, also named bladder cancer-related circular RNA-2 (BCRC-2), is significantly down-regulated in bladder cancer tissues and cell lines, and negatively correlates with bladder cancer grade, invasion as well as lymph node metastasis, respectively. Over-expression of circHIPK3 effectively inhibits migration, invasion, and angiogenesis of bladder cancer cells in vitro and suppresses bladder cancer growth and metastasis in vivo Mechanistic studies reveal that circHIPK3 contains two critical binding sites for the microRNA miR-558 and can abundantly sponge miR-558 to suppress the expression of heparanase (HPSE). Taken together, our findings provide evidence that circRNAs act as "microRNA sponges", and suggest a new therapeutic target for the treatment of bladder cancer.
Keyphrases
- gene expression
- poor prognosis
- long non coding rna
- endothelial cells
- rna seq
- cell proliferation
- lymph node metastasis
- spinal cord injury
- single cell
- long noncoding rna
- squamous cell carcinoma
- binding protein
- induced pluripotent stem cells
- cell migration
- muscle invasive bladder cancer
- genome wide
- vascular endothelial growth factor