| Literature DB >> 26573278 |
Elena Sebastián1,2,3, Miguel Alcoceba1,2,3, David Martín-García4, Óscar Blanco5, Mercedes Sanchez-Barba6, Ana Balanzategui1,2, Luis Marín1,2, Santiago Montes-Moreno3,7, Eva González-Barca3, Emilia Pardal3, Cristina Jiménez1, María García-Álvarez1, Guillem Clot4, Ángel Carracedo8,9, Norma C Gutiérrez1,2, M Eugenia Sarasquete1,2, Carmen Chillón1,2, Rocío Corral1,2, M Isabel Prieto-Conde1, M Dolores Caballero1,2,3, Itziar Salaverria4, Ramón García-Sanz10,11,12,13, Marcos González1,2,14.
Abstract
Copy number analysis can be useful for assessing prognosis in diffuse large B cell lymphoma (DLBCL). We analyzed copy number data from tumor samples of 60 patients diagnosed with DLBCL de novo and their matched normal samples. We detected 63 recurrent copy number alterations (CNAs), including 33 gains, 30 losses, and nine recurrent acquired copy number neutral loss of heterozygosity (CNN-LOH). Interestingly, 20 % of cases acquired CNN-LOH of 6p21 locus, which involves the HLA region. In normal cells, there were no CNAs but we observed CNN-LOH involving some key lymphoma regions such as 6p21 and 9p24.1 (5 %) and 17p13.1 (2.5 %) in DLBCL patients. Furthermore, a model with some specific CNA was able to predict the subtype of DLBCL, 1p36.32 and 10q23.31 losses being restricted to germinal center B cell-like (GCB) DLBCL. In contrast, 8p23.3 losses and 11q24.3 gains were strongly associated with the non-GCB subtype. A poor prognosis was associated with biallelic inactivation of TP53 or 18p11.32 losses, while prognosis was better in cases carrying 11q24.3 gains. In summary, CNA abnormalities identify specific DLBCL groups, and we describe CNN-LOH in germline cells from DLBCL patients that are associated with genes that probably play a key role in DLBCL development.Entities:
Keywords: CNA; CNN-LOH; Diffuse large B cell lymphoma; GC; Non-GC; Paired samples
Mesh:
Year: 2015 PMID: 26573278 DOI: 10.1007/s00277-015-2552-3
Source DB: PubMed Journal: Ann Hematol ISSN: 0939-5555 Impact factor: 3.673