| Literature DB >> 19321746 |
Stephan Mathas1, Stephan Kreher, Karen J Meaburn, Korinna Jöhrens, Björn Lamprecht, Chalid Assaf, Wolfram Sterry, Marshall E Kadin, Masanori Daibata, Stefan Joos, Michael Hummel, Harald Stein, Martin Janz, Ioannis Anagnostopoulos, Evelin Schrock, Tom Misteli, Bernd Dörken.
Abstract
Although the identification and characterization of translocations have rapidly increased, little is known about the mechanisms of how translocations occur in vivo. We used anaplastic large cell lymphoma (ALCL) with and without the characteristic t(2;5)(p23;q35) translocation to study the mechanisms of formation of translocations and of ALCL transformation. We report deregulation of several genes located near the ALCL translocation breakpoint, regardless of whether the tumor contains the t(2;5). The affected genes include the oncogenic transcription factor Fra2 (located on 2p23), the HLH protein Id2 (2p25), and the oncogenic tyrosine kinase CSF1-receptor (5q33.1). Their up-regulation promotes cell survival and repression of T cell-specific gene expression programs that are characteristic for ALCL. The deregulated genes are in spatial proximity within the nuclear space of t(2;5)-negative ALCL cells, facilitating their translocation on induction of double-strand breaks. These data suggest that deregulation of breakpoint-proximal genes occurs before the formation of translocations, and that aberrant transcriptional activity of genomic regions is linked to their propensity to undergo chromosomal translocations. Also, our data demonstrate that deregulation of breakpoint-proximal genes has a key role in ALCL.Entities:
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Year: 2009 PMID: 19321746 PMCID: PMC2667034 DOI: 10.1073/pnas.0900912106
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205