miR-31 Functions as an Oncomir Which Promotes Epithelial-Mesenchymal Transition via Regulating BAP1 in Cervical Cancer.

MicroRNA-31 (miR-31) functions as tumor suppressors or oncogenes that are involved in tumor behavior. However, the function of miR-31 in cervical carcinogenesis remains unclear. The aim of this study was to validate the potential role of miR-31 and BRCA1-associated protein-1 (BAP1) on regulating epi...

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Published in:BioMed Research International Vol. 2017; pp. 1 - 13
Main Authors: Wang, Nan, Li, Yong, Zhou, Jianhong
Format: pictorial research tables/charts Journal Article
Published: Wiley-Blackwell 10/11/2017
Online Access:View this record in EBSCOhost
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      dt: 10/11/2017
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      pub: Wiley-Blackwell
      place: Malden, Massachusetts
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        10.1155/2017/6361420
        125597012
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        atl: miR-31 Functions as an Oncomir Which Promotes Epithelial-Mesenchymal Transition via Regulating BAP1 in Cervical Cancer.
      aug:
        au:
          Wang, Nan
          Li, Yong
          Zhou, Jianhong
        affil: Laboratory of Molecular Biology, College of Life Science, Jiaying University, Meizhou 514015, China
      sug:
        subj:
          MicroRNA
          Cervix Neoplasms Familial and Genetic
          Gene Expression
          Human
          Polymerase Chain Reaction
          In Vivo Studies
          Xenografts
      ab: MicroRNA-31 (miR-31) functions as tumor suppressors or oncogenes that are involved in tumor behavior. However, the function of miR-31 in cervical carcinogenesis remains unclear. The aim of this study was to validate the potential role of miR-31 and BRCA1-associated protein-1 (BAP1) on regulating epithelial-mesenchymal transition (EMT) in cervical cancer. In the present study, qRT-PCR assay revealed that the expression of miR-31 was upregulated in human cervical cancer cells and clinical tissues. Results of wound healing and cell migration assay revealed that knockdown of miR-31 inhibited cell metastasis and migration. Bioinformatic and dual-luciferase reporter gene assay showed that BAP1 was the direct target of miR-31. Furthermore, the results revealed that miR-31 promoted proliferation and EMT in cervical cancer cells and accelerated the development of tumor growth in vivo xenograft experiment by inhibiting BAP1 expression. Overall, these results highlight an important role of miR-31 functioning as an oncomir which could promote EMT in cervical cancer via downregulating BAP1 expression. Thus, downregulation of miR-31 could be a novel approach for the molecular treatment of cervical cancers and other malignancies.
      pubtype: Academic Journal
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        research
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        Journal Article
      ougenre: Article
    language: English
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