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前列腺癌细胞中PDEF表达降低会增加其侵袭能力及间充质基因的表达。

Reduced PDEF expression increases invasion and expression of mesenchymal genes in prostate cancer cells.

作者信息

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

机构信息

BIDMC Genomics Center, Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, Massachusetts 02115, USA.

出版信息

Cancer Res. 2007 May 1;67(9):4219-26. doi: 10.1158/0008-5472.CAN-06-3689.

Abstract

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.

摘要

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。

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