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BIC and miR‐155 are highly expressed in Hodgkin, primary mediastinal and diffuse large B cell lymphomas

The Journal of Pathology · 2005 · Vol. 207(2) · pp. 243–249
Joost KluiverSibrand PoppemaDebora de JongTjasso BlokzijlGeert HarmsS. JacobsBart‐Jan KroesenAnke van den Berg

Abstract

In a previous study we demonstrated high expression of the non-coding BIC gene in the vast majority of Hodgkin's lymphomas (HLs). Evidence suggesting that BIC is a primary microRNA transcript containing the mature microRNA-155 (miR-155) as part of a RNA hairpin is now accumulating. We therefore analysed HL cell lines and tissue samples to determine whether miR-155 is also expressed in HL. High levels of miR-155 could be demonstrated, indicating that BIC is processed into a microRNA in HL. Most non-HL subtypes were negative for BIC as determined by RNA-ISH. However, in diffuse large B cell lymphoma (DLBCL) and primary mediastinal B cell lymphoma (PMBL), significant percentages of positive tumour cells were observed in 12/18 and 8/8 cases. A higher proportion of tumour cells were positive for BIC in DLBCL with activated B cell-like phenotype than in DLBCL with germinal centre B cell-like phenotype. Differential BIC expression was confirmed by qRT-PCR analysis. Northern blot analysis showed expression of miR-155 in all DLBCL and PMBL derived cell lines and tissue samples analysed. In summary, we demonstrate expression of primary microRNA BIC and its derivative miR-155 in HL, PMBL and DLBCL.

Lymphoma Diagnosis and TreatmentRNA Research and SplicingCancer-related molecular mechanisms researchmiR-155MedicinePathologyPrimary (astronomy)BiologymicroRNAPhysicsGeneGenetics

MeSH terms

Hodgkin DiseaseHumansImmunohistochemistryLymphomaMediastinal NeoplasmsReceptors, Antigen, B-CellRNA, NeoplasmLymphoma, B-CellLymphoma, Large B-Cell, DiffuseIn Situ HybridizationReverse Transcriptase Polymerase Chain ReactionMicroRNAsCell Line, Tumor
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