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CircHIPK3 sponges miR-558 to suppress heparanase expression in bladder cancer cells.


ABSTRACT: 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.

SUBMITTER: Li Y 

PROVIDER: S-EPMC5579470 | biostudies-literature | 2017 Sep

REPOSITORIES: biostudies-literature

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CircHIPK3 sponges miR-558 to suppress heparanase expression in bladder cancer cells.

Li Yawei Y   Zheng Fuxin F   Xiao Xingyuan X   Xie Fei F   Tao Dan D   Huang Chao C   Liu Dong D   Wang Miao M   Wang Liang L   Zeng Fuqing F   Jiang Guosong G  

EMBO reports 20170809 9


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  ...[more]

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