| Literature DB >> 15334547 |
Xin Ying Su1, Maryvonne Busson, Véronique Della Valle, Paola Ballerini, Nicole Dastugue, Pascaline Talmant, Adolfo A Ferrando, Dominique Baudry-Bluteau, Serge Romana, Roland Berger, Olivier A Bernard.
Abstract
Most chromosomal translocations observed in T-cell acute lymphoblastic leukemia (T-ALL) often produce transcriptional activation of transcription factor oncogenes. Ectopic expression of the TLX3 (also known as HOX11L2) gene has been shown to be associated with a cryptic t(5;14)(q35;q32) translocation specific for a subtype of T-ALL. Here we report several examples of variant and alternative translocations resulting in expression of TLX3 in T-ALL, and we describe three of these translocations in detail. In particular, the CDK6 gene was rearranged in two t(5;7)(q35;q21) translocations. In two additional instances, fusion of the BCL11B (also known as CTIP2) and RANBP17/TLX3 loci were shown to result from subtle genomic insertion/deletion within these loci. This study further underscores that TLX3 expression in T-ALL is strongly associated with the presence of genomic rearrangements. Copyright 2004 Wiley-Liss, Inc.Entities:
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Year: 2004 PMID: 15334547 DOI: 10.1002/gcc.20088
Source DB: PubMed Journal: Genes Chromosomes Cancer ISSN: 1045-2257 Impact factor: 5.006