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A Novel Non-Immunoglobulin (non-Ig)/BCL6 Translocation in Diffuse Large B-Cell Lymphoma Involving Chromosome 10q11.21 Loci and Review on Clinical Consequences of BCL6 Rearrangements
M. Jarosova, E. Kriegova, P. Schneiderova, R. Fillerova, V. Prochazka, M. Mikesova, P. Flodr, K. Indrak, T. Papajik,
Language English Country Netherlands
Document type Case Reports, Journal Article, Research Support, Non-U.S. Gov't, Review
NLK
ProQuest Central
from 1997-03-01 to 2019-01-31
Medline Complete (EBSCOhost)
from 2014-01-01
Nursing & Allied Health Database (ProQuest)
from 1997-03-01 to 2019-01-31
Health & Medicine (ProQuest)
from 1997-03-01 to 2019-01-31
ROAD: Directory of Open Access Scholarly Resources
from 1995
- MeSH
- Lymphoma, Large B-Cell, Diffuse genetics MeSH
- Gene Rearrangement * MeSH
- Middle Aged MeSH
- Humans MeSH
- Chromosomes, Human, Pair 10 genetics MeSH
- Prognosis MeSH
- Proto-Oncogene Proteins c-bcl-6 genetics MeSH
- Translocation, Genetic genetics MeSH
- Check Tag
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Publication type
- Journal Article MeSH
- Case Reports MeSH
- Research Support, Non-U.S. Gov't MeSH
- Review MeSH
BCL6 rearrangements (3q27) are the most common chromosomal abnormalities in diffuse large B-cell lymphoma (DLBCL), with numerous immunoglobulin (Ig) and non-Ig genes as partners. In DLBCL, the translocations occur predominantly in the "major breakpoint region" encompassing the first noncoding exon and a part of the first intron of BCL6; few cases with "alternative breakpoint cluster" located 245-285 kb 5' BCL6 were also described. The regulatory sequences of known Ig and non-Ig partners replace the 5' untranslated region of the BCL6 in the same transcriptional orientation. Contrary to Ig/BCL6 fusions typical by high BCL6 gene expression, in non-Ig/BCL6 translocations were observed unexpectedly low BCL6 mRNA levels. From the clinical point of view, the survival rate of DLBCL patients with non-Ig partners is inferior to those with Ig/BCL6 translocations, suggesting that non-Ig/BCL6 fusion is a poor prognostic indicator. Hereby we provide comprehensive information about known non-Ig translocation partners and clinical consequences of BCL6 rearrangements in DLBCL. Moreover, we describe a novel reciprocal translocation t(3;10) in refractory patient with DLBCL with the breaking points at 5' untranslated region of BCL6 and 5' untranslated region of the RASGEF1A gene on chromosome 10q11.21 loci; this rearrangement was associated with low BCL6 and RASGEF1A gene expressions. Our patient harbouring dual chromosomal rearrangement involving BCL2 and BCL6 genes relapsed three-times and died soon; thus, further supporting the notion that non-Ig/BCL6 fusion is a poor prognostic indicator of DLBCL. There is evidence of prognostic value of BCL6 rearrangements also in rituximab era.
References provided by Crossref.org
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