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TGF-ß induced miR-132 enhances the activation of TGF-ß signaling through inhibiting SMAD7 expression in glioma cells.
Wang, Zhao-hui; Zhang, Qi-shun; Duan, Yan-li; Zhang, Jian-lei; Li, Guo-fei; Zheng, Dong-lin.
Afiliación
  • Wang ZH; Department of Internal Neurology, Huaihe Hospital of Henan University, Kaifeng, 475000, China. Electronic address: wzhkf0526@163.com.
  • Zhang QS; Department of Internal Neurology, Huaihe Hospital of Henan University, Kaifeng, 475000, China.
  • Duan YL; Department of Ultrasonography, Obstetrics and Gynecology Hospital of Kaifeng, Kaifeng, 475000, China.
  • Zhang JL; Department of Internal Neurology, Huaihe Hospital of Henan University, Kaifeng, 475000, China.
  • Li GF; Department of Internal Neurology, Huaihe Hospital of Henan University, Kaifeng, 475000, China.
  • Zheng DL; Department of Internal Neurology, Huaihe Hospital of Henan University, Kaifeng, 475000, China.
Biochem Biophys Res Commun ; 463(3): 187-92, 2015 Jul 31.
Article en En | MEDLINE | ID: mdl-25983322
ABSTRACT
Transforming growth factors ß (TGF-ß) pathway has been proven to play important roles in oncogenesis and angiogenesis of gliomas. MiR-132 might be related to TGF-ß signaling pathway and high miR-132 expression was reported to be a biomarker of poor prognosis in patients diagnosed with glioma. However, the expression regulation way involved in TGF-ß pathway and clinical significance of miR-132 have not been investigated in glioma cells. Here we reported that the mRNA level of miR-132 and TGF-ß concentration were both increased in patients with brain glioma. Correlation analysis revealed that TGF-ß concentration was positively correlated with mRNA level of miR-132. In addition, the mRNA level of miR-132 was up-regulated by TGF-ß in a concentration-dependent and time-dependent manner. Furthermore, we found that miR-132 was involved in modulation of the TGF-ß signaling pathway and down-regulation of SMAD7 expression by directly targeting the SMAD7 3'-UTR. MiR-132 was negatively correlated with SMAD7 in patients with brain glioma. Taken together, our results suggest that miR-132 could be stimulated by TGF-ß and might enhance the activation of TGF-ß signaling through inhibiting SMAD7 expression in glioma cells. These findings contribute to a better understanding of the mechanism of the activation of TGF-ß signaling by miR-132.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Neoplasias Encefálicas / Regulación Neoplásica de la Expresión Génica / Factor de Crecimiento Transformador beta / MicroARNs / Proteína smad7 / Glioma Tipo de estudio: Prognostic_studies Límite: Female / Humans / Male Idioma: En Revista: Biochem Biophys Res Commun Año: 2015 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Neoplasias Encefálicas / Regulación Neoplásica de la Expresión Génica / Factor de Crecimiento Transformador beta / MicroARNs / Proteína smad7 / Glioma Tipo de estudio: Prognostic_studies Límite: Female / Humans / Male Idioma: En Revista: Biochem Biophys Res Commun Año: 2015 Tipo del documento: Article