Ryan K M, Birnie G D
Beatson Institute for Cancer Research, Cancer Research Campaign Beatson Laboratories, Bearsden, Glasgow, UK.
Oncogene. 1997 Jun 12;14(23):2835-43. doi: 10.1038/sj.onc.1201124.
The c-myc proto-oncogene has been shown to cause blockages to differentiation in many cell lineages. Although the mechanism by which c-Myc affects this process remains unknown, it is considered that it might result indirectly as an outcome of the continued cell-cycle progression invoked by c-Myc in cells which must growth arrest in order to differentiate. However, as there is little evidence to support this hypothesis, it is equally possible that a differentiation blockage occurs through a mechanism independent of c-Myc's involvement in cell-cycle progression. To explore this possibility we utilised a differentiation-defective variant of the U937 cell line, which still responds to the differentiation inducer by undergoing rapid growth arrest. Analysis of this line during growth arrest revealed that, although the expression of the Myc target gene, ornithine decarboxylase (ODC) was down-regulated, the cells differed from those of the parental line in that they continued to express high levels of c-Myc protein, but did not maintain high levels of expression of the Myc antagonists, mad1 and mxi1. Moreover, antisense down-regulation of the c-Myc protein levels in these growth-arrested cells revealed that this continued c-Myc expression was essential for their differentiation blockage. These data therefore indicate that c-Myc can block differentiation by a mechanism dissociated from its ability to direct cell-cycle progression or the expression of ODC.
c-myc原癌基因已被证明在许多细胞谱系中会导致分化受阻。尽管c-Myc影响这一过程的机制尚不清楚,但人们认为这可能是c-Myc在必须生长停滞才能分化的细胞中引发细胞周期持续进展的间接结果。然而,由于几乎没有证据支持这一假设,分化受阻也同样可能是通过一种独立于c-Myc参与细胞周期进展的机制发生的。为了探究这种可能性,我们利用了U937细胞系的一个分化缺陷变体,该变体仍能通过快速生长停滞对分化诱导剂作出反应。在生长停滞期间对该细胞系的分析表明,尽管Myc靶基因鸟氨酸脱羧酶(ODC)的表达下调,但这些细胞与亲代细胞系不同,它们继续高水平表达c-Myc蛋白,但没有维持Myc拮抗剂mad1和mxi1的高水平表达。此外,在这些生长停滞的细胞中对c-Myc蛋白水平进行反义下调表明,这种持续的c-Myc表达对于它们的分化受阻至关重要。因此,这些数据表明,c-Myc可以通过一种与其指导细胞周期进展或ODC表达能力无关的机制来阻断分化。