| Literature DB >> 19471018 |
Ellen Leich1, Itziar Salaverria, Silvia Bea, Andreas Zettl, George Wright, Victor Moreno, Randy D Gascoyne, Wing-Chung Chan, Rita M Braziel, Lisa M Rimsza, Dennis D Weisenburger, Jan Delabie, Elaine S Jaffe, Andrew Lister, Jude Fitzgibbon, Louis M Staudt, Elena M Hartmann, Hans-Konrad Mueller-Hermelink, Elias Campo, German Ott, Andreas Rosenwald.
Abstract
Follicular lymphoma (FL) is genetically characterized by the presence of the t(14;18)(q32;q21) chromosomal translocation in approximately 90% of cases. In contrast to FL carrying the t(14;18), their t(14;18)-negative counterparts are less well studied about their immunohistochemical, genetic, molecular, and clinical features. Within a previously published series of 184 FLs grades 1 to 3A with available gene expression data, we identified 17 FLs lacking the t(14;18). Comparative genomic hybridization and high-resolution single nucleotide polymorphism (SNP) array profiling showed that gains/amplifications of the BCL2 gene locus in 18q were restricted to the t(14;18)-positive FL subgroup. A comparison of gene expression profiles showed an enrichment of germinal center B cell-associated signatures in t(14;18)-positive FL, whereas activated B cell-like, NFkappaB, proliferation, and bystander cell signatures were enriched in t(14;18)-negative FL. These findings were confirmed by immunohistochemistry in an independent validation series of 84 FLs, in which 32% of t(14;18)-negative FLs showed weak or absent CD10 expression and 91% an increased Ki67 proliferation rate. Although overall survival did not differ between FL with and without t(14;18), our findings suggest distinct molecular features of t(14;18)-negative FL.Entities:
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Year: 2009 PMID: 19471018 PMCID: PMC2716022 DOI: 10.1182/blood-2009-01-198580
Source DB: PubMed Journal: Blood ISSN: 0006-4971 Impact factor: 22.113