P21 activated kinase-1 mediates transforming growth factor beta 1-induced prostate cancer cell epithelial to mesenchymal transition

摘要

Transforming growth factor beta (TGF beta) is believed to play a dual role in prostate cancer. Molecular mechanism by which TGF beta 1 suppresses early prostate tumor growth and induces epithelial-to-mesenchymal transition (EMT) in advanced stages is not known. We determined if P21-activated kinase1 (Pak1), which mediates cytoskeletal remodeling is necessary for the TGF beta 1 induced prostate cancer EMT. Effects of TGF beta 1 on control prostate cancer PC3 and DU145 cells and those with IPA 3 and siRNA mediated Pak1 inhibition were tested for prostate tumor xenograft in vivo and EMT in vitro. TGF beta 1 inhibited PC3 tumor xenograft growth via activation of P38-MAPK and caspase-3, 9. Long-term stimulation with TGF beta 1 induced PC3 and DU145 cell scattering and increased expression of EMT markers such as Snail and N-cadherin through tumor necrosis factor receptor-associated factor-6 (TRAF6)-mediated activation of Rac1/Pak1 pathway. Selective inhibition of Pak1 using IPA 3 or knockdown using siRNA both significantly inhibited TGF beta 1-induced prostate cancer cell EMT and expression of mesenchymal markers. Our study demonstrated that TGF beta 1 induces apoptosis and EMT in prostate cancer cells via activation of P38-MAPK and Rac1/Pak1 respectively. Our results reveal the potential therapeutic benefits of targeting TGF beta 1-Pak1 pathway for advanced-stage prostate cancer. (C) 2015 Elsevier B.V. All rights reserved.