You are currently visiting the test version of the radboud Dspace repository. To access the production instance, you can navigate to: https://repository.ubn.ru.nl

Fulltext:
87269.pdf
Embargo:
until further notice
Size:
86.73Kb
Format:
PDF
Description:
Publisher’s version
Publication year
2010Source
Cell Cycle, 9, 9, (2010), pp. 1711-6ISSN
Annotation
01 mei 2010
Publication type
Article / Letter to editor

Display more detailsDisplay less details
Organization
Cell Biology (UMC)
Journal title
Cell Cycle
Volume
vol. 9
Issue
iss. 9
Page start
p. 1711
Page end
p. 6
Subject
NCMLS 6: Genetics and epigenetic pathways of disease; ONCOL 3: Translational researchAbstract
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 wild-type 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.
This item appears in the following Collection(s)
- Academic publications [244578]
- Electronic publications [132441]
- Faculty of Medical Sciences [92890]
Upload full text
Use your RU or RadboudUMC credentials to log in with SURFconext to upload a file for processing by the repository team.