Gu Xuesong, Zerbini Luiz F, Otu Hasan H, Bhasin Manoj, Yang Quanli, Joseph Marie G, Grall Franck, Onatunde Tomi, Correa Ricardo G, Libermann Towia A
BIDMC Genomics Center, Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, Massachusetts 02115, USA.
Cancer Res. 2007 May 1;67(9):4219-26. doi: 10.1158/0008-5472.CAN-06-3689.
The epithelium-specific Ets transcription factor, PDEF, plays a role in prostate and breast cancer, although its precise function has not been established. In prostate cancer, PDEF is involved in regulating prostate-specific antigen expression via interaction with the androgen receptor and NKX3.1, and down-regulation of PDEF by antiproliferative agents has been associated with reduced PDEF expression. We now report that reduced expression of PDEF leads to a morphologic change, increased migration and invasiveness in prostate cancer cells, reminiscent of transforming growth factor beta (TGFbeta) function and epithelial-to-mesenchymal transition. Indeed, inhibition of PDEF expression triggers a transcriptional program of genes involved in the TGFbeta pathway, migration, invasion, adhesion, and epithelial dedifferentiation. Our results establish PDEF as a critical regulator of genes involved in cell motility, invasion, and adhesion of prostate cancer cells.
上皮特异性Ets转录因子PDEF在前列腺癌和乳腺癌中发挥作用,尽管其确切功能尚未明确。在前列腺癌中,PDEF通过与雄激素受体和NKX3.1相互作用参与调节前列腺特异性抗原的表达,抗增殖剂对PDEF的下调与PDEF表达降低有关。我们现在报告,PDEF表达降低会导致前列腺癌细胞发生形态学改变、迁移和侵袭能力增强,这让人联想到转化生长因子β(TGFβ)的功能以及上皮-间质转化。事实上,抑制PDEF表达会触发一个涉及TGFβ途径、迁移、侵袭、黏附及上皮去分化相关基因的转录程序。我们的结果表明,PDEF是参与前列腺癌细胞运动、侵袭和黏附相关基因的关键调节因子。