Williams Bret R, Prabhu Vineet R, Hunter Karen E, Glazier Christina M, Whittaker Charles A, Housman David E, Amon Angelika
David H. Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology (MIT), Cambridge, MA 02139, USA.
Science. 2008 Oct 31;322(5902):703-9. doi: 10.1126/science.1160058.
Aneuploidy, an incorrect number of chromosomes, is the leading cause of miscarriages and mental retardation in humans and is a hallmark of cancer. We examined the effects of aneuploidy on primary mouse cells by generating a series of cell lines that carry an extra copy of one of four mouse chromosomes. In all four trisomic lines, proliferation was impaired and metabolic properties were altered. Immortalization, the acquisition of the ability to proliferate indefinitely, was also affected by the presence of an additional copy of certain chromosomes. Our data indicate that aneuploidy decreases not only organismal but also cellular fitness and elicits traits that are shared between different aneuploid cells.
非整倍体,即染色体数目错误,是人类流产和智力迟钝的主要原因,也是癌症的一个标志。我们通过生成一系列携带四条小鼠染色体之一额外拷贝的细胞系,研究了非整倍体对原代小鼠细胞的影响。在所有四个三体细胞系中,增殖均受到损害,代谢特性也发生了改变。永生化,即获得无限增殖的能力,也受到某些染色体额外拷贝的影响。我们的数据表明,非整倍体不仅降低了机体适应性,还降低了细胞适应性,并引发了不同非整倍体细胞之间共有的特征。
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