| Literature DB >> 27423697 |
Mina Masoumeh Tayari1, Melanie Winkle1, Gertrud Kortman1, Jantine Sietzema1, Debora de Jong1, Martijn Terpstra2, Pieter Mestdagh3, Frans G M Kroese4, Lydia Visser1, Arjan Diepstra1, Klaas Kok2, Anke van den Berg1, Joost Kluiver5.
Abstract
Hodgkin lymphoma (HL) is a malignancy of germinal center (GC) B-cell origin. To explore the role of long noncoding RNAs (lncRNAs) in HL, we studied lncRNA expression patterns in normal B-cell subsets, HL cell lines, and tissues. Naive and memory B cells showed a highly similar lncRNA expression pattern, distinct from GC-B cells. Significant differential expression between HL and normal GC-B cells was observed for 475 lncRNA loci. For two validated lncRNAs, an enhanced expression was observed in HL, diffuse large B-cell lymphoma, and lymphoblastoid cell lines. For a third lncRNA, increased expression levels were observed in HL and part of Burkitt lymphoma cell lines. RNA fluorescence in situ hybridization on primary HL tissues revealed a tumor cell-specific expression pattern for all three lncRNAs. A potential cis-regulatory role was observed for 107 differentially expressed lncRNA-mRNA pairs localizing within a 60-kb region. Consistent with a cis-acting role, we showed a preferential nuclear localization for two selected candidates. Thus, we showed dynamic lncRNA expression changes during the transit of normal B cells through the GC reaction and widely deregulated lncRNA expression patterns in HL. Three lncRNAs showed a tumor cell-specific expression pattern in HL tissues and might therefore be of value as a biomarker.Entities:
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Year: 2016 PMID: 27423697 DOI: 10.1016/j.ajpath.2016.05.011
Source DB: PubMed Journal: Am J Pathol ISSN: 0002-9440 Impact factor: 4.307