Schmidt E V
MGH Cancer Center, Massachusetts General Hospital, Charlestown 02129, USA.
Oncogene. 1999 May 13;18(19):2988-96. doi: 10.1038/sj.onc.1202751.
Cell division is coupled to cell growth. Since some c-myc target genes are regulators of cell growth while others function in cell division pathways, c-myc is apparently poised at the interface of these processes. Cell culture systems have shown specific myc-associated growth phenotypes. Increased cell growth precedes DNA synthesis after myc activation in cells expressing myc-estrogen receptor fuson constructs and cells lacking c-myc exhibit a marked loss of protein synthesis. A number of candidate c-myc target genes regulate processes required for cell growth including rRNA transcription and processing, ribosomal protein transcription and translation, and translation initiation. These interactions all have the potential to account for the growth phenotypes in c-myc mutant cells. The ability of translation initiation factors, including eIF4E, to transform cells makes them particularly interesting targets of c-myc. Further evaluation of these target genes will provide important insights into growth control and c-myc's functions in cellular proliferation.
细胞分裂与细胞生长相关联。由于一些c-myc靶基因是细胞生长的调节因子,而其他一些则在细胞分裂途径中发挥作用,因此c-myc显然处于这些过程的交汇点。细胞培养系统已经显示出特定的与myc相关的生长表型。在表达myc-雌激素受体融合构建体的细胞中,myc激活后细胞生长增加先于DNA合成,而缺乏c-myc的细胞则表现出蛋白质合成的显著丧失。许多候选c-myc靶基因调节细胞生长所需的过程,包括rRNA转录和加工、核糖体蛋白转录和翻译以及翻译起始。这些相互作用都有可能解释c-myc突变细胞中的生长表型。包括eIF4E在内的翻译起始因子具有转化细胞的能力,这使得它们成为c-myc特别有趣的靶标。对这些靶基因的进一步评估将为生长控制和c-myc在细胞增殖中的功能提供重要见解。