| Literature DB >> 26726318 |
Nicholas A Willis1, Emilie Rass1, Ralph Scully1.
Abstract
Chromosome rearrangement plays a causal role in tumorigenesis by contributing to the inactivation of tumor suppressor genes, the dysregulated expression or amplification of oncogenes and the generation of novel gene fusions. Chromosome breaks are important intermediates in this process. How, when and where these breaks arise and the specific mechanisms engaged in their repair strongly influence the resulting patterns of chromosome rearrangement. Here, we review recent progress in understanding how certain distinctive features of the cancer genome, including clustered mutagenesis, tandem segmental duplications, complex breakpoints, chromothripsis, chromoplexy and chromoanasynthesis may arise.Entities:
Year: 2015 PMID: 26726318 PMCID: PMC4695301 DOI: 10.1016/j.trecan.2015.10.007
Source DB: PubMed Journal: Trends Cancer ISSN: 2405-8025