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CircURI1 interacts with hnRNPM to inhibit metastasis by modulating alternative splicing in gastric cancer.


ABSTRACT: Circular RNAs (circRNAs) have emerged as key regulators of human cancers, yet their modes of action in gastric cancer (GC) remain largely unknown. Here, we identified circURI1 back-spliced from exons 3 and 4 of unconventional prefoldin RPB5 interactor 1 (URI1) from circRNA profiling of five-paired human gastric and the corresponding nontumor adjacent specimens (paraGC). CircURI1 exhibits the significantly higher expression in GC compared with paraGC and inhibitory effects on cell migration and invasion in vitro and GC metastasis in vivo. Mechanistically, circURI1 directly interacts with heterogeneous nuclear ribonucleoprotein M (hnRNPM) to modulate alternative splicing of genes, involved in the process of cell migration, thus suppressing GC metastasis. Collectively, our study expands the current knowledge regarding the molecular mechanism of circRNA-mediated cancer metastasis via modulating alternative splicing.

SUBMITTER: Wang X 

PROVIDER: S-EPMC8379983 | biostudies-literature | 2021 Aug

REPOSITORIES: biostudies-literature

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<i>CircURI1</i> interacts with hnRNPM to inhibit metastasis by modulating alternative splicing in gastric cancer.

Wang Xiaolin X   Li Jingxin J   Bian Xing X   Wu Cheng C   Hua Jinghan J   Chang Shuhui S   Yu Tianyi T   Li Hong H   Li Yongxiang Y   Hu Shanshan S   Shan Ge G   Lin Wenchu W  

Proceedings of the National Academy of Sciences of the United States of America 20210801 33


Circular RNAs (circRNAs) have emerged as key regulators of human cancers, yet their modes of action in gastric cancer (GC) remain largely unknown. Here, we identified <i>circURI1</i> back-spliced from exons 3 and 4 of unconventional prefoldin RPB5 interactor 1 (URI1) from circRNA profiling of five-paired human gastric and the corresponding nontumor adjacent specimens (paraGC). <i>CircURI1</i> exhibits the significantly higher expression in GC compared with paraGC and inhibitory effects on cell m  ...[more]

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