Chromosome missegregation causes colon cancer by APC loss of heterozygosity

Darren J. Baker, Jan M. Van Deursen

Research output: Contribution to journalReview articlepeer-review

27 Scopus citations


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 ApcMin, 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.

Original languageEnglish (US)
Pages (from-to)1711-1716
Number of pages6
JournalCell Cycle
Issue number9
StatePublished - May 1 2010


  • Aneuploidy
  • Apc
  • Bub1
  • Colon cancer
  • Loss of heterozygosity
  • Mitotic checkpoint

ASJC Scopus subject areas

  • Molecular Biology
  • Developmental Biology
  • Cell Biology


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