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A new recurrent and specific cryptic translocation, t(5;14)(q35;q32), is associated with expression of the Hox11L2 gene in T acute lymphoblastic leukemia.

Authors
  • Bernard, O A
  • Busson-LeConiat, M
  • Ballerini, P
  • Mauchauffé, M
  • Della Valle, V
  • Monni, R
  • Nguyen Khac, F
  • Mercher, T
  • Penard-Lacronique, V
  • Pasturaud, P
  • Gressin, L
  • Heilig, R
  • Daniel, M T
  • Lessard, M
  • Berger, R
Type
Published Article
Journal
Leukemia
Publication Date
Oct 01, 2001
Volume
15
Issue
10
Pages
1495–1504
Identifiers
PMID: 11587205
Source
Medline
License
Unknown

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.

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