화학공학소재연구정보센터
Biochemical and Biophysical Research Communications, Vol.463, No.3, 187-192, 2015
TGF-beta induced miR-132 enhances the activation of TGF-beta signaling through inhibiting SMAD7 expression in glioma cells
Transforming growth factors beta (TGF-beta) pathway has been proven to play important roles in oncogenesis and angiogenesis of gliomas. MiR-132 might be related to TGF-beta 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-beta 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-beta concentration were both increased in patients with brain glioma. Correlation analysis revealed that TGF-beta concentration was positively correlated with mRNA level of miR-132. In addition, the mRNA level of miR-132 was up-regulated by TGF-beta in a concentration-dependent and time-dependent manner. Furthermore, we found that miR-132 was involved in modulation of the TGF-beta 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-beta and might enhance the activation of TGF-beta signaling through inhibiting SMAD7 expression in glioma cells. These findings contribute to a better understanding of the mechanism of the activation of TGF-beta signaling by miR-132. (C) 2015 Elsevier Inc. All rights reserved.