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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 :
E. Loraine Karran
Alexander Claviez
Stefan Gesk
Reiner Siebert
Keiji Sugimoto
Lana Harder
Takashi Akasaka
Inga Nagel
Lisa J. Russell
Fiona M. Ross
Helen Mazzullo
Martin J. S. Dyer
Jonathan C. Strefford
Anthony V. Moorman
Aneela Majid
Christine J. Harrison
Source :
Blood. 111(1)
Publication Year :
2007

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

ISSN :
00064971
Volume :
111
Issue :
1
Database :
OpenAIRE
Journal :
Blood
Accession number :
edsair.doi.dedup.....44f91ef6b38dfaf5e29b10e9584d1c42