Department of Biological Sciences, University of South Carolina, Columbia, South Carolina 29208, USA.
Cell Signal. 2012 Jan;24(1):316-24. doi: 10.1016/j.cellsig.2011.09.017. Epub 2011 Sep 22.
We previously identified FOXF1 as a potential tumor suppressor gene with an essential role in preventing DNA rereplication to maintain genomic stability, which is frequently inactivated in breast cancer through the epigenetic mechanism. Here we further addressed the role of the p53-p21(WAF1) checkpoint pathway in DNA rereplication induced by silencing of FOXF1. Knockdown of FOXF1 by small interference RNA (siRNA) rendered colorectal p53-null and p21(WAF1)-null HCT116 cancer cells more susceptible to rereplication and apoptosis than the wild-type parental cells. In parental HCT116 cells with a functional p53 checkpoint, the p53-p21(WAF1) checkpoint pathway was activated upon FOXF1 knockdown, which was concurrent with suppression of the CDK2-Rb cascade and induction of G(1) arrest. In contrast, these events were not observed in FOXF1-depleted HCT116-p53-/- and HCT116-p21-/- cells, indicating that the p53-dependent checkpoint function is vital for inhibiting CDK2 to induce G(1) arrest and protect cells from rereplication. The pharmacologic inhibitor (caffeine) of ataxia telangiectasia mutated (ATM) and ataxia telangiectasia and Rad3 related (ATR) protein kinases abolished activation of the p53-p21(WAF1) pathway upon FOXF1 knockdown, suggesting that suppression of FOXF1 function triggered the ATM/ATR-mediated DNA damage response. Cosilencing of p53 by siRNA synergistically enhanced the effect of FOXF1 depletion on the stimulation of DNA rereplication and apoptosis in wild-type HCT116. Finally, we show that FOXF1 expression is predominantly silenced in breast and colorectal cancer cell lines with inactive p53. Our study demonstrated that the p53-p21(WAF1) checkpoint pathway is an intrinsically protective mechanism to prevent DNA rereplication induced by silencing of FOXF1.
我们之前已经确定 FOXF1 是一种潜在的肿瘤抑制基因,在防止 DNA 重复制以维持基因组稳定性方面具有重要作用,而在乳腺癌中,这种基因通过表观遗传机制频繁失活。在这里,我们进一步研究了 p53-p21(WAF1)检查点途径在 FOXF1 沉默诱导的 DNA 重复制中的作用。通过小干扰 RNA(siRNA)敲低 FOXF1,使结直肠 p53 缺失和 p21(WAF1)缺失的 HCT116 癌细胞比野生型亲本细胞更容易发生重复制和凋亡。在具有功能性 p53 检查点的亲本 HCT116 细胞中,FOXF1 敲低后激活了 p53-p21(WAF1)检查点途径,同时抑制了 CDK2-Rb 级联并诱导 G1 期阻滞。相比之下,在 FOXF1 耗尽的 HCT116-p53-/-和 HCT116-p21-/-细胞中没有观察到这些事件,表明 p53 依赖性检查点功能对于抑制 CDK2 诱导 G1 期阻滞和保护细胞免受重复制至关重要。ATR 和 ATM 蛋白激酶的药理学抑制剂(咖啡因)抑制了 FOXF1 敲低后 p53-p21(WAF1)途径的激活,表明 FOXF1 功能的抑制触发了 ATM/ATR 介导的 DNA 损伤反应。siRNA 共沉默 p53 协同增强了 FOXF1 耗竭对野生型 HCT116 中 DNA 重复制和凋亡的刺激作用。最后,我们表明 FOXF1 在具有失活 p53 的乳腺癌和结直肠癌细胞系中主要被沉默。我们的研究表明,p53-p21(WAF1)检查点途径是一种内在的保护机制,可防止 FOXF1 沉默诱导的 DNA 重复制。