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      Follicular lymphomas with and without translocation t(14;18) differ in gene expression profiles and genetic alterations.

      Blood
      Chromosomes, Human, Pair 14, Chromosomes, Human, Pair 18, Cohort Studies, Comparative Genomic Hybridization, Gene Amplification, genetics, Gene Expression Profiling, Gene Expression Regulation, Neoplastic, Genetic Variation, Humans, Lymphoma, Follicular, Oligonucleotide Array Sequence Analysis, Polymorphism, Single Nucleotide, Proto-Oncogene Proteins c-bcl-2, metabolism, Translocation, Genetic

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          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.

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