Mai Sabine, Mushinski J Frederic
Manitoba Institute of Cell Biology, Cancer Care Manitoba, University of Manitoba, Winnipeg, Manitoba, Canada.
J Environ Pathol Toxicol Oncol. 2003;22(3):179-99. doi: 10.1615/jenvpathtoxoncol.v22.i3.30.
c-myc is one of a small family of proto-oncogenes that do not require mutation to contribute to neoplastic transformation. Instead, the deregulated expression of the oncoprotein at even modest levels is sufficient to initiate this process. The transforming activity of c-Myc is generally thought to lie in its ability to modulate the expression of a series of genes, among them certain proliferation-promoting genes. In reality, c-Myc is a multifunctional protein that also affects the stability of the genome. In this review, we summarize the growing evidence that deregulated c-myc expression generates genomic instability by initiating gene amplification (both intra- and extra-chromosomally), gene rearrangements, and karyotypic instability. Cancer is a disease of impaired genomic stability, to which c-Myc contributes during its initiation and progression through the induction of genomic instability in critical genes. Myc thus acts as a structural modifier of the genome and as a promoter of neoplastic transformation.
c-Myc是原癌基因小家族的成员之一,其无需发生突变就能促进肿瘤转化。相反,即使癌蛋白表达水平适度失调也足以启动这一过程。一般认为,c-Myc的转化活性在于其调节一系列基因表达的能力,其中包括某些促进增殖的基因。实际上,c-Myc是一种多功能蛋白,它还会影响基因组的稳定性。在本综述中,我们总结了越来越多的证据,即c-myc表达失调通过引发基因扩增(包括染色体内部和外部)、基因重排和核型不稳定而导致基因组不稳定。癌症是一种基因组稳定性受损的疾病,c-Myc在癌症的发生和发展过程中,通过诱导关键基因的基因组不稳定而发挥作用。因此,Myc既是基因组的结构修饰因子,也是肿瘤转化的促进因子。