Zimonjic D, Brooks M W, Popescu N, Weinberg R A, Hahn W C
Whitehead Institute for Biomedical Research, Cambridge, Massachusetts 02142, USA.
Cancer Res. 2001 Dec 15;61(24):8838-44.
The majority of adult human epithelial cancers exhibit evidence of genetic instability, and it is widely believed that the genetic instability manifested by aneuploidy or microsatellite instability plays an essential role in the genesis of these tumors. Indeed, most experimental models of cancer also show evidence of genomic instability. The resulting genetic chaos, which has widespread effects on many genes throughout the genome, confounds attempts to determine the precise cohort of genetic changes that are required for the transformation of normal human cells to a tumorigenic state. Here we show that genetic transformation of human kidney epithelial cells can occur in the absence of extensive aneuploidy, chromosomal translocations, and microsatellite instability. These observations demonstrate that the in vitro oncogenic transformation of human cells can proceed without widespread genomic instability.
大多数成人上皮性癌症表现出基因不稳定的迹象,人们普遍认为,非整倍体或微卫星不稳定性所表现出的基因不稳定在这些肿瘤的发生中起着至关重要的作用。事实上,大多数癌症实验模型也显示出基因组不稳定的迹象。由此产生的基因混乱对整个基因组中的许多基因都有广泛影响,这使得确定正常人类细胞转化为致瘤状态所需的确切基因变化群组的尝试变得复杂。在这里,我们表明人类肾上皮细胞的基因转化可以在没有广泛的非整倍体、染色体易位和微卫星不稳定性的情况下发生。这些观察结果表明,人类细胞的体外致癌转化可以在没有广泛基因组不稳定的情况下进行。