| Literature DB >> 11587205 |
O A Bernard1, M Busson-LeConiat, P Ballerini, M Mauchauffé, V Della Valle, R Monni, F Nguyen Khac, T Mercher, V Penard-Lacronique, P Pasturaud, L Gressin, R Heilig, M T Daniel, M Lessard, R Berger.
Abstract
FISH identified a cryptic t(5;14)(q35;q32) in T acute lymphoblastic leukemia (ALL), whereas it was not observed in B ALL samples. This translocation is present in five out of 23 (22%) children and adolescents with T ALL tested. RanBP17, a gene coding for a member of the importin beta protein family, and Hox11Like2, an orphan homeobox gene were mapped close to the chromosome 5 breakpoints and CTIP2, which is highly expressed during normal T cell differentiation, was localized in the vicinity of the chromosome 14 breakpoints. The Hox11L2 gene was found to be transcriptionally activated as a result of the translocation, probably under the influence of CTIP2 transcriptional regulation elements. These data establish the t(5;14)(q35;q32) as a major abnormality, and Hox11 family member activation as an important pathway in T ALL leukemogenesis.Entities:
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Year: 2001 PMID: 11587205 DOI: 10.1038/sj.leu.2402249
Source DB: PubMed Journal: Leukemia ISSN: 0887-6924 Impact factor: 11.528