Duke Institute for Genome Sciences & Policy, Duke University Medical Center, Durham, North Carolina, USA.
Cancer Res. 2010 Jun 15;70(12):4820-8. doi: 10.1158/0008-5472.CAN-10-0659. Epub 2010 Jun 1.
The Myc pathway, often deregulated in cancer, is critical in determining cell fate by coordinating a gene expression program that links the control of cell proliferation with cell fate decisions. As such, precise control of the Myc pathway activity must be achieved to ensure faithful execution of appropriate cellular response and to prevent progressing toward a malignant state. With recent highlighted roles of microRNAs (miRNA) as critical components of gene control, we sought to evaluate the extent to which miRNAs may contribute in the execution of Myc function. Combined analysis of mRNA and miRNA expression profiles reveals an integration whereby the Myc-mediated induction of miRNAs leads to the repression of various mRNAs encoding tumor suppressors that block cell proliferation including p21, p27, and Rb. In addition, the proapoptotic PTEN tumor suppressor gene is also repressed by Myc-induced miRNAs, suggesting that Myc-induced miRNAs contribute to the precise control of a transcriptional program that coordinates the balance of cell proliferation and cell death.
Myc 通路在癌症中经常失调,通过协调一个基因表达程序,将细胞增殖的控制与细胞命运决定联系起来,从而对细胞命运起着决定性作用。因此,必须精确控制 Myc 通路的活性,以确保细胞能够执行适当的反应,防止向恶性状态发展。鉴于 microRNAs(miRNA)作为基因调控关键成分的最新突出作用,我们试图评估 miRNA 在执行 Myc 功能方面可能起到的作用。mRNA 和 miRNA 表达谱的综合分析揭示了一种整合方式,即 Myc 介导的 miRNA 诱导导致各种编码肿瘤抑制因子的 mRNA 被抑制,这些抑制因子阻止细胞增殖,包括 p21、p27 和 Rb。此外,促凋亡的 PTEN 肿瘤抑制基因也被 Myc 诱导的 miRNA 抑制,这表明 Myc 诱导的 miRNA 有助于精确控制协调细胞增殖和细胞死亡平衡的转录程序。