| Literature DB >> 11895757 |
James Z Huang1, Warren G Sanger, Timothy C Greiner, Louis M Staudt, Dennis D Weisenburger, Diane L Pickering, James C Lynch, James O Armitage, Roger A Warnke, Ash A Alizadeh, Izidore S Lossos, Ronald Levy, Wing C Chan.
Abstract
Recently we have identified subgroups of de novo primary diffuse large B-cell lymphoma (DLBCL) based on complementary DNA microarray-generated gene expression profiles. To correlate the gene expression profiles with cytogenetic abnormalities in these DLBCLs, we examined the occurrence of the t(14;18)(q32;q21) in the 2 distinctive subgroups of DLBCL: one with the germinal center B-cell gene expression signature and the other with the activated B cell-like gene expression signature. The t(14;18) was detected in 7 of 35 cases (20%). All 7 t(14;18)-positive cases had a germinal center B-cell gene expression profile, representing 35% of the cases in this subgroup, and 6 of these 7 cases had very similar gene expression profiles. The expression of bcl-2 and bcl-6 proteins was not significantly different between the t(14;18)-positive and -negative cases, whereas CD10 was detected only in the group with the germinal center B-cell expression profile, and CD10 was most frequently expressed in the t(14;18)-positive cases. This study supports the validity of subdividing DLBCL into 2 major subgroups by gene expression profiling, with the t(14;18) being an important event in the pathogenesis of a subset of DLBCL arising from germinal center B cells. CD10 protein expression is useful in identifying cases of DLBCL with a germinal center B-cell gene expression profile and is often expressed in cases with the t(14;18).Entities:
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Year: 2002 PMID: 11895757 DOI: 10.1182/blood.v99.7.2285
Source DB: PubMed Journal: Blood ISSN: 0006-4971 Impact factor: 22.113