Chromosome missegregation causes colon cancer by APC loss of heterozygosity

被引:28
作者
Baker, Darren J. [1 ]
van Deursen, Jan M. [1 ,2 ]
机构
[1] Mayo Clin, Coll Med, Dept Pediat & Adolescent Med, Rochester, MN 55905 USA
[2] Mayo Clin, Coll Med, Dept Mol Biol & Biochem, Rochester, MN USA
基金
美国国家卫生研究院;
关键词
Bub1; Apc(Min); mitotic checkpoint; loss of heterozygosity; colon cancer; aneuploidy; AGING-ASSOCIATED PHENOTYPES; SPINDLE CHECKPOINT; MITOTIC CHECKPOINT; TUMOR-SUPPRESSOR; MAMMALIAN-CELLS; INSTABILITY; MICE; ANEUPLOIDY; TUMORIGENESIS; BUB1;
D O I
10.4161/cc.9.9.11314
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
A longstanding hypothesis in the field of cancer biology is that aneuploidy causes cancer by promoting loss of chromosomes that contain tumor suppressor genes. By crossing aneuploidyprone Bub1 hypomorphic mice onto a heterozygous null background for p53, we provided conclusive evidence for this idea. 1 Surprisingly, the tumors that developed in this model had not just lost the chromosome 11 copy harboring wildtype p53, but had also gained an extra copy of chromosome 11 bearing the p53 null allele. Here we report that a similar chromosome-reshuffling blueprint drives colonic tumorigenesis in Bub1 hypomorphic mice that are heterozygous for Apc(Min), but now involving chromosome 18. These extended studies highlight that in order for whole chromosome instability to drive tumorigenesis, it needs to establish tumor suppressor gene loss of heterozygosity while retaining two copies of the other genes on the chromosome. Additional restrictions seem to apply to whole chromosome instability as a cancer causing mechanism, which will be discussed in this paper.
引用
收藏
页码:1711 / 1716
页数:6
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