Department of Experimental Pathology, Mayo Clinic College of Medicine, Rochester, MN, USA.
Oncogene. 2010 Mar 4;29(9):1362-73. doi: 10.1038/onc.2009.431. Epub 2009 Dec 7.
We have previously shown that a frequently downregulated gene, transcription elongation factor A-like 7 (TCEAL7), promoted anchorage-independent growth and modulated Myc activity in ovarian surface epithelial cells immortalized with temperature-sensitive large T antigen and human telomerase reverse transcriptase (OSEtsT/hTERT). Analysis of protein/DNA array showed that TCEAL7 downregulation resulted in an approximately twofold increase in nuclear factor (NF)-kappaB binding to its target DNA sequence. In this study we showed that short hairpin RNA (shRNA)-mediated downregulation of TCEAL7 in two different immortalized OSE cells showed higher NF-kappaB activity, as determined using reporter and gel-shift assays. Transient transfection of TCEAL7 inhibited the activation of NF-kappaB in TCEAL7-downregulated clones, IOSE-523 and in other ovarian cancer cell lines (OVCAR8, SKOV3ip and DOV13), suggesting that TCEAL7 negatively regulates NF-kappaB pathway. Consistent with this observation, TCEAL7-downregulated clones showed higher levels of NF-kappaB targets, such as pro-proliferative (cyclin-D1 and cMyc), pro-angiogenic (interleukin (IL)-6, IL-8 and vascular endothelial growth factor (VEGF)), inflammatory (intercellular adhesion molecule 1 (ICAM-1) and cyclooxygenase-2 (Cox-2)) and anti-apoptotic (B-cell lymphoma-extra large (Bcl-xl)) genes when compared with vector controls. Inhibition of NF-kappaB by IkappaB kinase (IKK) inhibitor (BMS 345541) attenuated cell survival and proliferation of TCEAL-knockdown clones. Although TCEAL7 inhibited p65 transcriptional activity, it did not modulate the cytoplasmic signaling of the NF-kappaB pathway, by itself or by tumor necrosis factor-alpha (TNF-alpha). Chromatin immunoprecipitation (ChIP) assays revealed increased recruitment of p65 and p300 to the promoters of IL-8 and IL-6 in TCEAL7-downregulated clones. Collectively, these results indicate a novel role for TCEAL7 in the negative regulation of NF-kappaB signaling at the basal level by modulating transcriptional activity of NF-kappaB on its target gene promoters, potentially providing a novel mechanism by which NF-kappaB activity may be deregulated in ovarian cancer cells.
我们之前已经表明,经常下调的基因转录延伸因子 A 样 7(TCEAL7)促进了温度敏感大 T 抗原和人端粒酶逆转录酶(OSEtsT/hTERT)永生化的卵巢表面上皮细胞的无锚定生长,并调节 Myc 活性。蛋白质/DNA 阵列分析表明,TCEAL7 的下调导致核因子(NF)-kappaB 与其靶 DNA 序列的结合增加约两倍。在这项研究中,我们表明,两种不同的永生化 OSE 细胞中短发夹 RNA(shRNA)介导的 TCEAL7 下调导致 NF-kappaB 活性更高,这通过报告基因和凝胶迁移分析来确定。TCEAL7 的瞬时转染抑制了 TCEAL7 下调克隆(IOSE-523 和其他卵巢癌细胞系(OVCAR8、SKOV3ip 和 DOV13)中 NF-kappaB 的激活,表明 TCEAL7 负调节 NF-kappaB 途径。与这一观察结果一致,TCEAL7 下调的克隆显示出更高水平的 NF-kappaB 靶标,例如促增殖(细胞周期蛋白-D1 和 cMyc)、促血管生成(白细胞介素(IL)-6、IL-8 和血管内皮生长因子(VEGF))、炎症(细胞间黏附分子 1(ICAM-1)和环氧化酶-2(Cox-2))和抗凋亡(B 细胞淋巴瘤-额外大(Bcl-xl))基因,与载体对照相比。IkappaB 激酶(IKK)抑制剂(BMS 345541)抑制 NF-kappaB 可减弱 TCEAL 敲低克隆的细胞存活和增殖。尽管 TCEAL7 抑制了 p65 的转录活性,但它本身或通过肿瘤坏死因子-α(TNF-α)都没有调节 NF-kappaB 途径的细胞质信号。染色质免疫沉淀(ChIP)分析显示,在 TCEAL7 下调的克隆中,p65 和 p300 募集到 IL-8 和 IL-6 启动子的增加。总的来说,这些结果表明 TCEAL7 在通过调节 NF-kappaB 对其靶基因启动子的转录活性,在基础水平上负调节 NF-kappaB 信号方面发挥了新的作用,这可能为 NF-kappaB 活性在卵巢癌细胞中失调提供了一种新的机制。