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MicroRNA-214 targets PCBP2 to suppress the proliferation and growth of glioma cells.
Tang, Shi-Lei; Gao, Yuan-Lin; Chen, Xiao-Bing.
Afiliação
  • Tang SL; Department of Neurosurgery, Huaihe Hospital, Henan University Kaifeng 475000, China.
  • Gao YL; Department of Neurology, Kaifeng Central Hospital Kaifeng 475000, China.
  • Chen XB; Department of Neurosurgery, Huaihe Hospital, Henan University Kaifeng 475000, China.
Int J Clin Exp Pathol ; 8(10): 12571-6, 2015.
Article em En | MEDLINE | ID: mdl-26722446
ABSTRACT
PCBP2, a member of the poly(C)-binding protein (PCBP) family, is involved in posttranscriptional and translational regulation by interacting with single-stranded poly(C) motifs in target mRNAs. Recent studies have shown that PCBP2 is overexpressed and plays an important role in human cancers, including glioma. However, the molecular basis for its up-regulation remains poorly understood. Here, we show that microRNA-214 (miR-214) interacts with the 3'-untranslated region of PCBP2 mRNA and induces its degradation, leading to reductions in its protein expression. As a result, overexpression of miR-214 mimics significantly inhibited, while its antisense oligos proliferation and growth of glioma cells. Restoration of PCBP2 remarkably reversed the tumor-suppressive effects of miR-214 on cell proliferation and growth. In summary, our data indicate that miR-214 may function as tumor suppressor in glioma by targeting PCBP2.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Encefálicas / Regulação Neoplásica da Expressão Gênica / Proteínas de Ligação a RNA / MicroRNAs / Proliferação de Células / Glioma Limite: Humans Idioma: En Revista: Int J Clin Exp Pathol Assunto da revista: PATOLOGIA Ano de publicação: 2015 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Encefálicas / Regulação Neoplásica da Expressão Gênica / Proteínas de Ligação a RNA / MicroRNAs / Proliferação de Células / Glioma Limite: Humans Idioma: En Revista: Int J Clin Exp Pathol Assunto da revista: PATOLOGIA Ano de publicação: 2015 Tipo de documento: Article País de afiliação: China