| Literature DB >> 23827691 |
Elise Chapiro1, Isabelle Radford-Weiss, Hong-Anh Cung, Nicole Dastugue, Nathalie Nadal, Sylvie Taviaux, Carole Barin, Stephanie Struski, Pascaline Talmant, Peter Vandenberghe, Marie-Joelle Mozziconacci, Isabelle Tigaud, Christine Lefebvre, Dominique Penther, Christian Bastard, Eric Lippert, Francine Mugneret, Serge Romana, Olivier A Bernard, Christine J Harrison, Lisa J Russell, Florence Nguyen-Khac.
Abstract
Chromosomal translocations involving the immunoglobulin heavy chain locus (IGH@) are recurrent but rare in B-cell precursor acute lymphoblastic leukemia (BCP-ALL), and various partner genes have been described. Here, we report a new series of 29 cases of BCP-ALL with IGH@ translocations. The partner gene was identified by fluorescence in situ hybridization and/or molecular cloning in 20 patients. Members of the CEBP gene family (n = 11), BCL2 (n = 3), ID4 (n = 3), EPOR (n = 2), and TRA/D@ (n = 1) were identified and demonstrated by quantitative real-time reverse transcriptase-polymerase chain reaction to be markedly up-regulated. The present cases, added to those already reported, confirm the diversity of the partner genes, which, apart from BCL2, are specific to BCP-ALL. Collectively, patients with IGH@ translocations may represent a novel sub-group of BCP-ALL occurring in adolescents and young adults.Entities:
Keywords: B-cell progenitor acute lymphoblastic leukemia; IGH@ translocations
Mesh:
Substances:
Year: 2013 PMID: 23827691 DOI: 10.1016/j.cancergen.2013.04.004
Source DB: PubMed Journal: Cancer Genet