Department of Molecular and Cellular Biology, Baylor College of Medicine, Houston, Texas 77030, USA.
J Biol Chem. 2010 Apr 9;285(15):11258-69. doi: 10.1074/jbc.M109.073932. Epub 2010 Feb 5.
The Ets family of transcription factors control a myriad of cellular processes and contribute to the underlying genetic loss of cellular homeostasis resulting in cancer. PDEF (prostate-derived Ets factor) has been under investigation for its role in tumor development and progression. However, the role of PDEF in cancer development has been controversial. Some reports link PDEF to tumor promoter, and others show tumor-suppressing functions in various systems under different conditions. So far, there has been no conclusive evidence from in vivo experiments to prove the role of PDEF. We have used both in vitro and in vivo systems to provide a conclusive role of PDEF in the progression process. PDEF-expressing cells block the cell growth rate, and this retardation was reversible when PDEF expression was silenced with PDEF-specific small interfering RNA. When these PDEF-expressing cells were orthotopically implanted into the mouse mammary gland, tumor incidence and growth rate were significantly retarded. Cell cycle analysis revealed that PDEF expression partially blocked cell cycle progression at G(1)/S without an effect on apoptosis. PDEF overexpression resulted in an increase in p21/CIP1 at both the mRNA and protein levels, resulting in decreased Cdk2 activity. Promoter deletion analysis, electrophoresis mobility shift assays, and chromatin immunoprecipitation studies identified the functional Ets DNA binding site at -2118 bp of the p21/CIP1 gene promoter. This site is capable of binding and responding to PDEF. Furthermore, we silenced p21/CIP1 expression in PDEF-overexpressing cells by small interfering RNA. p21-silenced PDEF cells exhibited significantly increased cell growth in vitro and in vivo, demonstrating the p21 regulation by PDEF as a key player. These experiments identified PDEF as a new transcription factor that directly regulates p21/CIP1 expression under non-stressed conditions. This study conclusively proves that PDEF is a breast tumor suppressor for the first time using both in vitro and in vivo systems. PDEF can be further developed as a target for designing therapeutic intervention of breast cancer.
Ets 转录因子家族控制着无数的细胞过程,并导致细胞稳态的潜在遗传丢失,从而导致癌症。PDEF(前列腺衍生的 Ets 因子)因其在肿瘤发生和发展中的作用而受到研究。然而,PDEF 在癌症发展中的作用一直存在争议。一些报告将 PDEF 与肿瘤促进剂联系起来,而另一些报告则显示在不同条件下的各种系统中具有肿瘤抑制功能。到目前为止,还没有来自体内实验的确凿证据证明 PDEF 的作用。我们使用体外和体内系统为 PDEF 在进展过程中的作用提供了确凿的证据。表达 PDEF 的细胞会阻止细胞生长速度,当用 PDEF 特异性小干扰 RNA 沉默 PDEF 表达时,这种抑制作用是可逆的。当这些表达 PDEF 的细胞被原位植入小鼠乳腺时,肿瘤的发生率和生长速度明显减慢。细胞周期分析显示,PDEF 表达部分阻止了细胞周期在 G1/S 期的进展,而对细胞凋亡没有影响。PDEF 过表达导致 p21/CIP1 在 mRNA 和蛋白质水平上的增加,从而导致 Cdk2 活性降低。启动子缺失分析、电泳迁移率变动分析和染色质免疫沉淀研究鉴定了 p21/CIP1 基因启动子-2118bp 处的功能性 Ets DNA 结合位点。该位点能够结合并响应 PDEF。此外,我们通过小干扰 RNA 沉默 PDEF 过表达细胞中的 p21/CIP1 表达。p21 沉默的 PDEF 细胞在体外和体内表现出明显增加的细胞生长,表明 PDEF 对 p21 的调节是关键因素。这些实验首次使用体外和体内系统证明 PDEF 是一种直接调节非应激条件下 p21/CIP1 表达的新型转录因子。这项研究首次使用体外和体内系统证明 PDEF 是一种直接调节非应激条件下 p21/CIP1 表达的新型转录因子。这项研究首次使用体外和体内系统证明 PDEF 是一种直接调节非应激条件下 p21/CIP1 表达的新型转录因子。这项研究首次使用体外和体内系统证明 PDEF 是一种直接调节非应激条件下 p21/CIP1 表达的新型转录因子。PDEF 可以进一步开发为设计乳腺癌治疗干预的靶点。