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Interplay between PCBP2 and miRNA modulates ARHGDIA expression and function in glioma migration and invasion.


ABSTRACT: RNA-RNA and protein-RNA interactions are essential for post-transcriptional regulation in normal development and may be deregulated in cancer initiation and progression. The RNA-binding protein PCBP2, an oncogenic protein in human malignant gliomas, is an essential regulator of mRNA and miRNA biogenesis, stability and activity. Here, we identified Rho GDP dissociation inhibitor ? (ARHGDIA) as a target mRNA that binds to PCBP2, and we uncovered the role of ARHGDIA as a putative metastasis suppressor through analyses of in vitro and in vivo models of EMT and metastasis. Furthermore, we demonstrated that ARHGDIA is a potential target of miR-151-5p and miR-16 in gliomas. The interaction between PCBP2 and the 3'UTR of the ARHGDIA mRNA may induce a local change in RNA structure that favors subsequent binding of miR-151-5p and miR-16, thus leading to the suppression of ARHGDIA expression. PCBP2 may facilitate miR-151-5p and miR-16 promotion of glioma cell migration and invasion through mitigating the function of ARHGDIA.

SUBMITTER: Lin X 

PROVIDER: S-EPMC4991396 | biostudies-literature | 2016 Apr

REPOSITORIES: biostudies-literature

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Interplay between PCBP2 and miRNA modulates ARHGDIA expression and function in glioma migration and invasion.

Lin Xihua X   Yang Bin B   Liu Wei W   Tan Xiaochao X   Wu Fan F   Hu Peishan P   Jiang Tao T   Bao Zhaoshi Z   Yuan Jiangang J   Qiang Boqin B   Peng Xiaozhong X   Han Wei W  

Oncotarget 20160401 15


RNA-RNA and protein-RNA interactions are essential for post-transcriptional regulation in normal development and may be deregulated in cancer initiation and progression. The RNA-binding protein PCBP2, an oncogenic protein in human malignant gliomas, is an essential regulator of mRNA and miRNA biogenesis, stability and activity. Here, we identified Rho GDP dissociation inhibitor α (ARHGDIA) as a target mRNA that binds to PCBP2, and we uncovered the role of ARHGDIA as a putative metastasis suppres  ...[more]

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