Author/Authors :
Bruna، نويسنده , , Alejandra and Darken، نويسنده , , Rachel S. and Rojo، نويسنده , , Federico and Ocaٌa، نويسنده , , Alberto and Peٌuelas، نويسنده , , Silvia and Arias، نويسنده , , Alexandra and Paris، نويسنده , , Raquel and Tortosa، نويسنده , , Avelina and Mora، نويسنده , , Jaume and Baselga، نويسنده , , José B. Seoane، نويسنده , , Joan، نويسنده ,
Abstract :
Summary
cts as a tumor suppressor in normal epithelial cells and early-stage tumors and becomes an oncogenic factor in advanced tumors. The molecular mechanisms involved in the malignant function of TGFβ are not fully elucidated. We demonstrate that high TGFβ-Smad activity is present in aggressive, highly proliferative gliomas and confers poor prognosis in patients with glioma. We discern the mechanisms and molecular determinants of the TGFβ oncogenic response with a transcriptomic approach and by analyzing primary cultured patient-derived gliomas and human glioma biopsies. The TGFβ-Smad pathway promotes proliferation through the induction of PDGF-B in gliomas with an unmethylated PDGF-B gene. The epigenetic regulation of the PDGF-B gene dictates whether TGFβ acts as an oncogenic factor inducing PDGF-B and proliferation in human glioma.
