| Literature DB >> 29196303 |
Rozario Thomas1,2, Daniel Henry Marks2, Yvette Chin2, Robert Benezra3,2.
Abstract
Whole chromosome gains or losses (aneuploidy) are a hallmark of ~70% of human tumors. Modeling the consequences of aneuploidy has relied on perturbing spindle assembly checkpoint (SAC) components, but interpretations of these experiments are clouded by the multiple functions of these proteins. Here, we used a Cre recombinase-mediated chromosome loss strategy to individually delete mouse chromosomes 9, 10, 12, or 14 in tetraploid immortalized murine embryonic fibroblasts. This methodology also involves the generation of a dicentric chromosome intermediate, which subsequently undergoes a series of breakage-fusion-bridge (BFB) cycles. While the aneuploid cells generally display a growth disadvantage in vitro, they grow significantly better in low adherence sphere-forming conditions and three of the four lines are transformed in vivo, forming large and invasive tumors in immunocompromised mice. The aneuploid cells display increased chromosomal instability and DNA damage, a mutator phenotype associated with tumorigenesis in vivo Thus, these studies demonstrate a causative role for whole chromosome loss and the associated BFB-mediated instability in tumorigenesis and may shed light on the early consequences of aneuploidy in mammalian cells.Entities:
Keywords: aneuploidy; chromosomal instability; chromosome losses; tetraploidy; tumorigenesis
Mesh:
Year: 2017 PMID: 29196303 PMCID: PMC5770879 DOI: 10.15252/embj.201797630
Source DB: PubMed Journal: EMBO J ISSN: 0261-4189 Impact factor: 11.598