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t(6;14)(p22;q32): a new recurrent IGH@ translocation involving ID4 in B-cell precursor acute lymphoblastic leukemia (BCP-ALL)

Authors :
Russell, Lisa J.
Akasaka, Takashi
Majid, Aneela
Sugimoto, Kei-ji
Loraine Karran, E.
Nagel, Inga
Harder, Lana
Claviez, Alexander
Gesk, Stefan
Moorman, Anthony V.
Ross, Fiona
Mazzullo, Helen
Strefford, Jonathan C.
Siebert, Reiner
Dyer, Martin J. S.
Harrison, Christine J.
Source :
Blood; January 2008, Vol. 111 Issue: 1 p387-391, 5p
Publication Year :
2008

Abstract

Translocations involving the immunoglobulin heavy chain locus (IGH@) at chromosome band 14q32 are common in mature B-cell neoplasms, but are rare in B-cell precursor acute lymphoblastic leukemia (BCP-ALL). Here, we report the translocation, t(6;14)(p22;q32), involving IGH@ as a novel recurrent translocation in 13 BCP-ALL patients. Fluorescence in situ hybridization and long-distance inverse polymerase chain reaction (PCR) identified ID4 as the partner gene. Breakpoints were scattered over a 19kb region centromeric of ID4. Quantitative real-time PCR showed up-regulation of ID4 mRNA. All patients had deletions of CDKN2A and PAX5 located on the short arm of chromosome 9, frequently as a result of an isochromosome, i(9)(q10) (9/13, 69%). This study defines a new subgroup of BCP-ALL characterized by ID4 over-expression and CDKN2A and PAX5 deletions. Preliminary survival data suggest that this subgroup may be associated with a good response to therapy.

Details

Language :
English
ISSN :
00064971 and 15280020
Volume :
111
Issue :
1
Database :
Supplemental Index
Journal :
Blood
Publication Type :
Periodical
Accession number :
ejs53040713
Full Text :
https://doi.org/10.1182/blood-2007-07-092015